Bing Xu, Brandeis University
Shawn Chen, National Institute of Biomedical Imaging and Bioengineering
Honggang Cui, The Johns Hopkins University
Brandeis University, MRSEC, MilliporeSigma (Sigma-Aldrich Materials Science), Cell Press
BM1.1: Young Investigators
Monday AM, November 28, 2016
Hynes, Level 1, Room 102
9:30 AM - BM1.1.01
Molecular Engineering of Polymeric Materials for Innovative Medical Solutions
Shiyi Zhang 1
1 Shanghai Jiao Tong University Shanghai ChinaShow Abstract
The innovative engineering methodologies that allow for the preparation of functional polymer materials by simple strategies have significant fundamental interest and enormous potential to address unmet clinical needs. This talk will focus on the design principle that is simple, novel and applicable, for the development of polymeric materials for distinct applications. In treating three pulmonary diseases, two degradable nanoparticle systems based on one functional polyphosphoester will be discussed, with the highlight of the simple, efficient and versatile chemistry involved in each stage of the production. For the prolonged gastric retention with improved safety profile, the development of three polymer systems will be presented, giving the emphasis to a novel pH-responsive supramolecular gel that helped to achieve a 5-7 days gastric retention in a large animal model promising the application to solve the poor medication adherence.
9:45 AM - BM1.1.02
Refilling Drug-Eluting Hydrogels through Systemic Administration of Inert Prodrugs
Yevgeny Brudno 1 , David Mooney 1 , Michael Aizenberg 1
1 Harvard University Cambridge United StatesShow Abstract
Drug-eluting material systems have proven useful in a variety of clinical settings, including preventing restenosis with stenting, treating cancer and enhancing wound healing. These systems benefit from tunable drug release kinetics, continuous drug release, and local delivery, which together provide spatiotemporal control over drug availability and diminish drug toxicity. I will describe our efforts to overcome one major hurdle to widespread use of drug-eluting systems in vivo – that they carry a finite depot of drug and require invasive procedures to refill. I will describe a technology to modify materials so as to capture blood-circulating drug refills, allowing for repeated refilling of the depots for local release. Bioorthogonal chemistry and nucleic acid-based methods for selective depot replenishment will be discussed. Repeated drug refilling and release improved outcomes in cancer models and allowed for selective drug homing in models of lower limb ischemia and osteomyelitis. Refillable drug delivery devices that enable repeated and spatiotemporally controlled drug release may have clinical applications in cancer therapy, wound healing, immunotherapy, and drug-eluting vascular grafts and stents.
10:00 AM - BM1.1.03
Synthesis, Assembly and Characterization of POMaC Elastomer Used in Biodegradable Strain and Pressure Sensor for Tendons Recovery Monitoring
Clementine Boutry 1 , Anais Legrand 1 , Bob Schroeder 2 , Zhenan Bao 1
1 Stanford University Stanford United States, 2 Queen Mary University of London London United KingdomShow Abstract
New biosensors, entirely made of biodegradable materials and designed for being implanted in the human body, are currently emerging. These sensors open the field for new therapeutic applications, without need for a second surgery to remove the devices after their predefined period of use. The development of new spatiotemporally-controlled biomaterials is required for being used in such sensors.
In the present work, we investigate the use of the biodegradable elastomer POMaC in a new stretchable strain and pressure sensor developed in the context of tendons recovery monitoring. This biomaterial is used both as a key structural and packaging material. Various synthesis approaches, combining exposure to UV irradiation (photocrosslinked POMaC) and oven curing (polycondensation crosslinked POMaC), are evaluated. The material response to long-term mechanical cycling before and after in vitro degradation in PBS solution is also investigated. We show in particular that the tensile modulus and resistance to cycling of POMaC can be adjusted using an appropriate synthesis approach, to better fit the final therapeutic application. Moreover, a strategy for the final packaging of the sensor based on sealing with UV-exposed prePOMaC is investigated. We show efficient packaging properties, with negligible sensor signal variation after hours of immersion in PBS solution.
Our investigations on the synthesis and assembly of this biodegradable elastomer permit the development of a sensor with high sensitivity, fast response time and long-term stability, allowing its use in the context of tendon tissues recovery monitoring.
10:15 AM - BM1.1.04
Design of Self-Assembling Bio-Inks for Cell-Based 3D Printing
Karen Dubbin 1 , Yuki Hori 1 , Kazuomori Lewis 1 , Sarah Heilshorn 1
1 Stanford University Stanford United StatesShow Abstract
Despite the rise of 3D printing of thermoplastics both in industry and the general public, a key limitation preventing the widespread use of cell-based 3D printing is the lack of suitable bio-inks that are cell-compatible and have the required properties for printing. Current commonly used biomaterials have distinct limitations when used as a bio-ink including difficulty maintaining a homogeneous cell suspension, avoiding cell damage during extrusion, customizing the printed matrix properties to facilitate cell-matrix interactions, and printing within a bath to prevent cell dehydration while preserving high print resolution. We designed a new family of tunable biomaterials specifically designed for cell-based 3D printing. These hydrogel-based bio-inks are produced from a blend of engineered recombinant proteins and peptide-modified, alginate polysaccharides. The use of engineered proteins provides control of ligand presentation for cellular attachment and signaling, while the alginate enables cyto-compatible, rapid crosslinking within a hydrated sample. This design is advantageous due to the ability of the bio-ink to undergo two-stages of crosslinking: (i) weak, peptide-based, self-assembly to homogeneously encapsulate cells within the ink cartridge, to prevent cell settling in the print cartridge, and to mechanically shield the cells from damaging forces during extrusion and (ii) electrostatic crosslinking of alginate upon printing within a calcium bath to rapidly stabilize the construct and to tailor the final mechanical properties for optimal cell-matrix interactions with full cell hydration.
10:30 AM - BM1.1.05
Enzyme-Triggered Peptide Folding and Self-Assembly of Phosphopeptides
Junfeng Shi 1 , Joel Schneider 1
1 National Cancer Institute Frederick United StatesShow Abstract
Enzymatic transformation is essential mechanism for signal transduction in the cell. In this work, we report the use of enzyme to regulate the peptide folding and self-assembly, thus induced the supramolecular hydrogelation. HPLC and LC-MS analysis identify that the designed phosphopeptide is the substrate of protein phosphatase. Circular dichroism (CD) spectra show the enzyme is able to modulate the rate of peptide folding and self-assembly. Electron microscopy reveals that the enzymatic reaction converts the unfolding peptide to protofibrils, and nanofibrils. Rheology confirmed the formation of stable hydrogel. As the first case of enzyme-triggered peptide folding and self-assembly, this work not only provide an approach to generate sophisticated materials, but also offer insight how to modulate the interaction of peptide and cellular environment.
10:45 AM - BM1.1.06
Programmable Self-Assembly of Peptide-Polymer Hybrid Hydrogels
Daniel Aili 1 , Christopher Aronsson 1 , Robert Selegard 1 , Staffan Danmark 1
1 Department of Physics, Chemistry and Biology Linköping University Linköping SwedenShow Abstract
Hydrogels are attractive as cell carriers and bioinks in injection-based therapies and 3D bioprinting as they can protect cells from damaging shear forces during the injection or the additive manufacturing process. Hydrogels can also offer extracellular matrix mimicking environments for both tissue engineering applications and 3D cell culture. Different applications and processing conditions require hydrogels with significantly different properties. To this end, we have established a flexible modular strategy for fabrication of supramolecular hydrogels that offer means to tightly control both the self-assembly process as well as the mechanical and structural properties of the hydrogels. A set of different modular peptide-polymer hybrids have been synthesized using de novo designed peptides that dimerize and fold into well-defined alpha-helical motifs.[1,2] The peptides were grafted to four-arm PEGs and hyaluronic acid using click chemistry. Self-assembly of physical hydrogels was triggered by peptide dimerization and folding. The properties of the hydrogels can be rationally and dynamically modulated using peptides with different affinities for dimerization and by complexation of cations. In addition to offer means to dynamically assemble and disassemble the hydrogels, the storage modulus of the hydrogels can be varied from about 200 to 1000 Pa when using peptides with affinities for dimerization spanning from the nanomolar to the picomolar range. This novel strategy thus enables fabrication of dynamic stimuli-responsive soft materials for biomedical applications with properties that can be programmed using defined and tunable peptide-mediated interactions.
 D. Aili, F.-I. Tai, K. Enander, L. Baltzer, B. Liedberg, “Self-assembling fibers and nano-rings from disulphide linked helix-loop-helix polypeptides”, Angew. Chem., Int. Ed., 2008, 47, 5554-5556.
 C. Aronsson, S. Dånmark, F. Zhou, P. Öberg, K. Enander, H. Su, D. Aili, "Self-Sorting Heterodimeric Coiled Coil Peptides with Defined and Tuneable Self-Assembly Properties”, Sci. Rep., 2015, 5, 14063; doi:10.1038/srep14063.
 S. Dånmark, C. Aronsson, D. Aili, "Tailoring Supramolecular Peptide-Poly(ethylene glycol) Hydrogels by Coiled Coil Self-Assembly and Self-Sorting", Biomacromolecules, 2016, 17, 2260–2267.
11:30 AM - BM1.1.07
Tie Up Actin Cytoskeleton to Suppress Cancer Metastasis
Ye Zhang 1
1 Okinawa Institute of Science and Technology Kunigami-gun JapanShow Abstract
Cancer therapeutics that are designed to inhibit metastasis by targeting signaling pathways have not proven to be effective in clinical trials because cancer cells can modify their migration mechanism in response to different conditions. To cope with the dynamic transform, we developed a novel access to inhibit metastasis by tying up actin cytoskeleton through physical interaction for restriction of cancer cell migration by mechanical force. We designed and synthesized multi-dimensional luminescent molecules that self-assemble into nanoscale morphologies and selectively forms extracellular matrix (ECM) on ovarian cancer cell filopodia. The ECM fixate adhesion receptors and block their redistribution. The actin skeleton linked with adhesion receptors were tied up results into physically restrained cancer cell deformability and migration.
11:45 AM - BM1.1.08
Three-Dimensional Micro-Patterning of Biodegradable Polymers for Controlled Drug Delivery
Thanh Nguyen 1 , Robert Langer 2
1 University of Connecticut Storrs United States, 2 Koch Institute Massachusetts Institute of Technology Cambridge United StatesShow Abstract
The ability to create three-dimensional (3D) biomaterial structures with high resolution and aspect-ratio enables significant biomedical applications. Numerous methods including 3D printing technologies have been developed to fabricate microdevices and particles with well-defined 3D structure. However, these techniques are limited in terms of shape, aspect ratio, scalability, and either require potentially toxic additives or lack the fine resolution demanded for some applications. Here we present a novel method - termed StampEd Assembly of polymer Layers (SEAL) - which can create versatile 3D microstructures of pure biodegradable polymers such as poly-lactic-glycolid acid (PLGA), and use this method to create a robust drug delivery platform with unique pulsatile release kinetics. SEAL combines computer-chip manufacturing technologies, micromolding, and a novel layer-by-layer assembly process to fabricate 3D microstructures of biomedically relevant materials without processing additives. We employed SEAL to create PLGA/drug core-shell microparticles for controlled drug delivery applications. These SEAL-fabricated particles exhibited delayed, pulsatile release for up to 2 months, which is particularly exciting to the development of single-injection vaccines. We also demonstrate the use of SEAL for creating particles using an enteric polymer that exhibits pH-dependent release following oral administration for selective colon targeting. Finally, we show that the SEAL method is compatible with sensitive biomacromolecules such as the highly instable inactivated polio vaccine (IPV). As such, SEAL is a powerful method that can supplement 3D printing when high resolution, high-throughput, and biocompatibility are required for proper device function. We anticipate many applications from this platform technology such as the creation of 3D tissue synthetic scaffolds with well-defined microstructure and injectable drug delivery devices with unique targeting or release kinetics based on complex 3D architecture and/or material composition.
12:00 PM - BM1.1.09
Membrane-Embedded Nanoparticles Facilitate the Rapid Translocation of Charged Species across Lipid Bilayers
Reid Van Lehn 1
1 University of Wisconsin-Madison Madison United StatesShow Abstract
Functionalized nanoparticles (NPs) are versatile materials with heterogeneous surface properties that can be engineered to mimic typical biological macromolecules. Recently, a particular class of charged, amphiphilic NPs were shown to embed within lipid bilayers to obtain configurations similar to transmembrane proteins. Embedding involves the dynamic rearrangement of NP surface properties to adapt to the bilayer environment. This behavior is surprising, however, because the NPs must also transport charged groups across the hydrophobic bilayer core within short timescales to stably insert into the bilayer. Here, we use atomistic molecular dynamic simulations to gain a mechanistic understanding of this rapid charge transport. We show that charged species grafted to a bilayer-embedded scaffold – such as the NPs or multispanning transmembrane proteins – translocate across the bilayer more rapidly than isolated ions. We further study the system features that affect translocation rates in order to identify methods to facilitate the translocation of specific charged groups. This work suggests design guidelines for synthetic materials capable of transporting charged, soluble small molecules across bilayers, which may be useful for ferrying therapeutic molecules to the interior of cells for drug delivery applications.
12:15 PM - BM1.1.10
Micro-Robotic Devices for Localized Actuation and Selective Positioning
in the Gastrointestinal Tract
Jinxing Li 1 , Soracha Kun Thamphiwatana 1 , Liangfang Zhang 1 , Joseph Wang 1
1 University of California, San Diego La Jolla United StatesShow Abstract
Robotics deals with automated machines that can locomote themselves and operate tasks in various environments over many orders of magnitudes in scale. One of the most inspiring goals is the construction of smart and powerful nanorobotic systems for operation in the human body. However, viscous forces dominate inertial forces at such small scales, leading to the “low-Reynolds number challenge” for nanoscale propulsion. This presentation will discuss newly created multi-functional nanorobots which can overcome this challenge by utilizing local chemical reactions to achieve efficient movement in biological matrices. With selectively engineered materials, the nanorobots possess numerous attractive properties, including biocompatibility, biodegradability, high loading capacity, and the ability to autonomously release of payloads ‘on-the-fly’. The increased capabilities and sophistication of these tiny robots hold considerable promise for a variety of biomedical applications ranging from drug delivery to minimally invasive surgery. Particularly, using zinc-based micromotors as model robots, we reported the first in vivo study of artificial micromotors in a living organism. Such in vivo evaluation examines the distribution, retention, cargo delivery, and acute toxicity profile of synthetic motors in mouse stomachs via oral administration. We demonstrate that the acid-driven propulsion in the stomach effectively enhances the binding and retention of the motors as well as of cargo payloads on the stomach wall.
In another design, we demonstrate an enteric micromotor system capable of precise positioning and controllable retention in desired segments of the Gastrointestinal (GI) tract. These motors, consisting of magnesium-based tubular micromotors coated with an enteric polymer layer, act as a robust nanobiotechnology tool for site-specific GI delivery. The micromotors can deliver payload to particular location via dissolution of their enteric coating to activate their propulsion at the target site towards localized tissue penetration and retention. Our work is anticipated to significantly advance the emerging field of biomedical nanorobots and to open the door to in vivo evaluation and clinical applications of these biomedical nanorobots.
 Artificial Micromotors in the Mouse’s Stomach: A Step toward in Vivo Use of Synthetic Motors. ACS Nano, 2015, 9, 117–123.
 An Enteric Micromotor can Selectively Position and Spontaneously Propel in the Gastrointestinal Tract. Submitted to Nature Mater.
12:30 PM - *BM1.1.11
Targeting Siglecs with a Sialic Acid-Decorated Nanoparticle Abrogates Inflammation
Michelle Greene 1 , Shaun Spence 1 , Francois Fay 3 , Emily Hams 2 , Sean Saunders 2 , Umar Hamid 1 , Marianne Fitzgerald 1 , Cecilia O'Kane 1 , Denise Fitzgerald 1 , James Johnston 4 , Padraic Fallon 2 , Daniel McAuley 1 , Adrien Kissenpfennig 1 , Christopher Scott 1
1 Queen's University Belfast Belfast United Kingdom, 3 Icahn School of Medicine at Mount Sinai New York United States, 2 Trinity College Dublin Dublin Ireland, 4 Amgen Inc. Thousand Oaks United StatesShow Abstract
Sepsis is the most common cause of death in hospitalised patients, with an annual incidence of 1 million cases and 200,000 deaths in the USA alone1. Moreover, approximately 25% of sepsis cases are complicated by the development of Acute Respiratory Distress Syndrome (ARDS), which also incurs a high mortality rate2. Both sepsis and ARDS are characterised by excessive pro-inflammatory responses, for which there are currently no effective treatments. Instead, supportive therapy within the critical care setting forms the mainstay of treatment and so novel therapeutic strategies are urgently required.
Given the fundamental role of sialic acid-binding immunoglobulin-like lectins (Siglecs) in modulating immune responses, these receptors represent potential anti-inflammatory targets in sepsis and ARDS. In particular, previous studies demonstrated that engagement of murine Siglec-E negatively regulates Toll-like receptor (TLR)-mediated inflammation3. In this current work, a novel sialylated nanoparticle was developed to actively target Siglec receptors expressed on macrophages, with potential therapeutic utility in sepsis and ARDS.
Polylactic-co-glycolic acid (PLGA) nanoparticles were formulated via a salting-out approach and decorated with α2,8 N-acetylneuraminic acid targeting moieties (α2,8 NANA-NP). Physicochemical characterisation of α2,8 NANA-NP revealed an average diameter of 152 ± 13 nm and a polydispersity index of 0.16 ± 0.08, indicative of a monodisperse size distribution. When tested in cultures of lipopolysaccharide (LPS)-stimulated murine macrophages, α2,8 NANA-NP potently inhibited the secretion of pro-inflammatory tumour necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) cytokines in a Siglec-E dependent manner. Therapeutic efficacy was also confirmed in both systemic and pulmonary in vivo models of inflammation, where α2,8 NANA-NP enhanced survival rates, attenuated neutrophil infiltration, inhibited pro-inflammatory cytokine production and augmented anti-inflammatory IL-10 levels, amongst other readouts. Mechanistic studies uncovered that the functionality of α2,8 NANA-NP was both macrophage- and IL-10-dependent, given the loss of efficacy in clodronate-treated and IL-10 knockout mice, respectively. Moreover, the translational potential of this nanoplatform was demonstrated in cultures of primary human monocytes and macrophages, and also in a human ex vivo lung perfusion model, where α2,8 NANA-NP significantly attenuated LPS-induced inflammation.
Collectively, these findings demonstrate that the targeted cross-linking and activation of Siglecs can be exploited therapeutically in models of sepsis and ARDS. In addition to these syndromes, α2,8 NANA-NP may also find potential application in other conditions underpinned by aberrant pro-inflammatory signalling.
1 Immunity 2014, 40(4), 463-75
2 Intensive Care Med 2004, 30(1), 51-61
3 J Immunol 2009, 183(12), 7703-9
Monday PM, November 28, 2016
Hynes, Level 1, Room 102
2:30 PM - *BM1.2.01
Surface-Engineered Nanocrystals—Synthesis, Assembly, and Applications
Peng Wang 1 , Qirong Xiong 1 , Jiajing Zhou 1 , Hongwei Duan 1
1 Nanyang Technological University Singapore SingaporeShow Abstract
Inorganic nanocrystals with unique optical, electronic, magnetic, and structural properties have found widespread use in biosensing, bioimaging, surface-enhanced spectroscopy, drug delivery, and catalysis. Organization of the nanocrystals into superstructures often leads to collective properties that are different from those in the discrete units. Controlled assembly of the nanocrystals is currently under intense research and development for a wide range of applications in electronic devices, biosensing, and drug delivery. This talk summarizes our recent results in developing plasmonic and magnetic superstructures for cancer diagnostic and therapeutic applications. Metallic nanostructures with localized surface plasmon resonance arising from the collective excitation of conduction electrons LSPR spectral shifts induced by interparticle plasmonic coupling have attracted considerable research interest in controlled assembly of plasmonic nanoparticles, which, in conjugation with responsive “smart” coatings, has been exploited to detect a wide range of molecular targets and environmental factors. We have developed versatile approaches to engineer nanoparticle surface with polymer ligands and assemble the nanoparticles into well-defined structures in aqueous dispersion and at oil-water interfaces, which hold great promise in traceable drug delivery, surface enhanced Raman scattering, and biosensing. We have developed a new approach, built upon the use of mussel-inspired polydopamine, to preparing robust multifunctional nanochains of magnetic nanoparticles with readily tailorable surface chemistry for applications in different environments. We have found that the resulting rigid magnetic nanochains undertake localized rotation when placed in a spinning magnetic field, making it possible for the nanochains to serve as nanomotors and nanoscale stir bars to promote molecular transport and mixing in extremely small spaces, which is highly desirable for applications in microreactors and ultrasmall sensing devices. More interestingly, conjugation of DNA aptamer ligands of specific receptors overexpressed on cancer cell membrane led to targeted nanochains that bound to selective cancer cells, and subsequent exposure to a spinning magnetic field caused pronounced cell death via magnetolysis of cell membranes.
3:00 PM - *BM1.2.02
Membrane Fusion Delivery of siRNA Using Nanoparticle Nanocapsules—Applications of Direct Cytosol Delivery In Vitro and In Vivo
Vincent Rotello 1
1 University of Massachusetts Amherst United StatesShow Abstract
Therapeutic delivery of proteins and nucleic acids is a difficult goal. Of the many challenges in the delivery process, perhaps the most demanding is providing these biologics with access to the cytosol. Most delivery strategies employ endosomal uptake, requiring endosomal escape for the payload biologics to be effective. In our research, we have developed an alternative strategy that uses nanoparticle-stabilized nanocapsules (NPSCs) to deliver proteins and nucleic acids (siRNA and DNA) directly to the cytosol. These NPSCs use a membrane fusion process to bypass the endosomal pathway, providing highly effective payload delivery. The direct access to the cytosol makes NPSCs effective tools for therapeutic delivery, particularly in conjunction with intracellular targeting. Mechanistic studies of NPSCs and their use in vivo for immunomodulation will be discussed.
3:30 PM - BM1.2.03
Diagnosis of Tropical Viruses Using Gold Nanoparticles in Lateral Flow Immunoassays
Helena de Puig Guixe 1 , Marc Carre-Camps 1 , Irene Bosch 1 , Kimberly Hamad-Schifferli 2 , Lee Gehrke 1
1 Massachusetts Institute of Technology Cambridge United States, 2 University of Massachusetts Boston United StatesShow Abstract
In the currently ongoing outbreak, zika (ZIKV) is co-circulating with dengue virus (DENV) and chikungunya (CHKV), which also share the same vector, the mosquitoes Aedes aegypti and Aedes albopictus. Infection by any of the three diseases leads to similar flu-like symptoms, complicating proper disease management. Point-of-care diagnostics are critically needed for rapid response in patient treatment, resource allocation and to predict epidemics. Lateral flow devices are ideal candidates to diagnose diseases in remote areas because they can be operated by non-experts, are cheap, portable, and do not require electric power to be operated. We present results on a machine-readable multiplexed lateral flow device for the detection of several tropical disease markers. By making the device readable by a mobile phone, it is able to provide real-time epidemiologic data to monitor disease distribution. The device relies on a lateral flow immunoassay, which uses capillary flow and the accumulation of ligand-coated nanoparticles to detect the presence of target proteins. Gold nanoparticle-antibody conjugates are critical to ensure that the device will have enough sensitivity to detect the illness even at low concentrations of target protein, such as in early stages of the disease. The sensitivity of lateral flow devices greatly depends on the nature of the ligand-target pair and their binding thermodynamics on the nanoparticle interface. We engineer the nanoparticle shape, size, surface chemistry, and biofunctionalization in order to lower the overall detection limit of the device. The nanoparticle surface properties and biofunctionalization are characterized by gel electrophoresis, DLS, and fluorescence/optical spectroscopy in conjunction with chemical displacement.
These new, effective, low-cost devices would be very useful in developing countries, but also for developed countries, where they can contribute to lowering the overall cost of healthcare and enable widespread use for other applications such as crowdsourcing.
3:45 PM - BM1.2.04
Overcoming the Blood-Brain Barrier—Post-Resection Drug Delivery to Glioblastoma Multiforme Using Supramolecular Hydrogels
Oren Scherman 1
1 University of Cambridge Cambridge United KingdomShow Abstract
Glioblastoma multiforme (GBM) is a devastating disease with extremely poor survival statistics owing to high rates of disease recurrence. Typical treatment of patients diagnosed with GBM is surgical resection of accessible tumorous tissue followed by radiotherapy and chemotherapy. Chemotherapeutic choices are limited on account of most drugs’ poor propensity to cross the blood brain barrier. Systemic treatment with unspecified concentrations of chemotherapy is ineffective and risks adverse side effects. An alternative approach involves the use of supramolecular hydrogels, which can be readily loaded with therapeutic agents for sustained localized delivery.
High water content (99%) and biocompatible hydrogels based on hyaluronic acid (HA) backbones developed within the our group rely on non-covalent cross-links between polymers, formed by utilizing the dynamic host-guest chemistry of cucurbituril (CB). In this system, amino acid derived “guest moieties” that are bound to HA polymers complex in a 2:1 fashion with a “host-molecule” CB, creating multiple cross-links resulting in gelation. As these complexes are non-covalent they can be broken with mechanical stress and instantly reformed upon relaxation due to fast binding kinetics. This material can encapsulate water-soluble drug compounds, be injected through a needle and rapidly self heal preventing any cargo loss. Tissue strength and elasticity can also be replicated in the hydrogel properties by simply modulating the polymer or CB concentration.
In vitro release studies of various drug compounds encapsulated in the hydrogel have been performed and efficacy against multiple patient-derived human GBM cell lines determined. In vivo experiments with a mouse model are currently underway. We envisage that access to such drug-delivery technology will lead to clinical studies in the near future with an overall goal to prevent disease recurrence and improve patient survival rates.
4:30 PM - *BM1.2.05
Intra-Mitochondrial Assembly of Peptide Amphiphiles as Novel Cancer Therapy
Ja-Hyoung Ryu 1 , M. T. Jeena 1
1 Ulsan National Institute of Science and Technology Ulsan Korea (the Republic of)Show Abstract
Mitochondria are vital organelles to eukaryotic cells. Since damage and dysfunction of mitochondria cause cell apoptosis, mitochondrial specific targeting gains lots of interest in cancer therapeutics. Delivery of cancer specific drug into mitochondria has already been established in recent years by various approaches such as conjugation of drug molecule with mitochondria targeting ligands. However, mitochondrial damage due to self-assembly of amphiphilic molecules inside mitochondria still remains challenging. It is already well proved that peptides have intrinsic ability to form various self-assembled structure such as fiber, ribbon, sphere and vesicle. Study of selfassembling behavior of peptide inside the live cell organelle is least established till now. Here, we introduce mitochondria targeting short peptide containing sequence as Py-FFK(TPP) [Py = Pyrenebutyric acid, TPP = Triphenyl phosphonium, F = phenyl alanine, K = lysine]. The TPP moiety can provide mitochondrial specific targeting to mitochondria and pyrene butyric acid provides both a self-assembling building block and a fluorescent probe. The peptide exhibited well-defined morphology in water, high mitochondrial localization and cancer-cell cytotoxicity. The improved mitochondrial localization of peptide is attributed to the TPP moiety and high hydrophobicity. Under the mitochondrial environment the peptide can undergo aggregation due to increased concentration above the critial aggregation cocnetraion (40 uM). The self-assembly of the peptide induces mitochondrial stress and thereby generates ROS and causes cell death.
5:00 PM - *BM1.2.06
Durable Bio-Inert Coating for Biomedical Applications
Xinhua Li 1
1 Nano Terra, Inc Cambridge United StatesShow Abstract
A surface that can suppress nonspecific binding and resist biofouling is critical for the performance of biomedical and analytical devices. A number of bio-inert chemical functions has been identified using self-assembled monolayers (SAM). Significant effort has been made to apply these chemistries in the development of biomedical products; however, a durable and easy to use bio-inert coating is still lacking. We developed coating formulations for the treatment of various surfaces to reduce protein binding and cell adhesion. We demonstrated that the bio-inert coating is stable under gamma irradiation and the treated plastic surface strongly resists adhesion of various cells including 3T3, MCF-7 and MDA-MB-231.
5:30 PM - *BM1.2.07
The Art of Falling Apart—Exploiting Nanomaterial Disassembly for Health Sciences
Adah Almutairi 1
1 University of California, San Diego La Jolla United StatesShow Abstract
This presentation will cover several recent advances in the development of light- and inflammation-responsive polymers as tools for biological research and drug delivery. In the area of light-responsive materials, four exciting strategies will be discussed: chemically amplifying the light signal to accelerate degradation, single-photon absorption of red light, novel upconverting structures enabling efficient conversion of more biologically compatible wavelengths, and application of previously reported polymers to the treatment of various diseases. The chemical amplification strategy relies on phototriggered unmasking of acidic groups that hydrolyze adjacent ketals, which overcomes ketals’ requirement of low pH for efficient degradation. Particles composed of the photocaged-acid/ ketal polymer degrade rapidly upon brief irradiation. The red light-degradable polymer incorporates a photocage not previously used in responsive materials, which cleaves in hydrophobic environments (unlike coumarins). Particles composed of this polymer, when subcutaneously injected and irradiated through tissue, release sufficient drug to significantly reduce carrageenan-induced paw inflammation in mice. Finally, we have evidence that a UV-degradable polymer (Fomina et al., J Am Chem Soc 2010) may be useful for the delivery of anti-angiogenics in the eye to treat macular degeneration. This strategy would preserve clinician control over dose timing while reducing the frequency of intravitreal injections. UV-degradable particles are stable in the eye for months and release a therapeutically effective dose of a small molecule anti-angiogenic; the irradiation required for release is well-tolerated by the eye.
Inflammation-responsive materials have been recently applied in the lab towards prevention of systemic inflammatory response syndrome (SIRS), treatment of Age Related Macular Degeneration with a single annual injection of a drug depot of VEGF Trap and detection of atherosclerotic plaque likely to disrupt and cause a heart attack or stroke. The first project involves delivering anti-inflammatory drugs in nanoparticles composed of our polythioether ketal (published in 2011). Using this strategy to deliver drugs 12 h prior to the bacterial toxin LPS reduces mortality in mice, suggesting that such nanoparticles could lead to a means of preventing organ failure following systemic infection or trauma. In the second, particles composed of dextran modified to be acid- and H2O2-responsive encapsulate Gd-based nanocrystals with unprecedented relaxivity, such that MRI signal is silenced until encountering inflammation, where particles loosen and nanocrystals can relax surrounding water molecules. This material’s ability to detect inflammation in vivo has been demonstrated using fluorescence activation;
Bing Xu, Brandeis University
Shawn Chen, National Institute of Biomedical Imaging and Bioengineering
Honggang Cui, The Johns Hopkins University
Brandeis University, MRSEC, MilliporeSigma (Sigma-Aldrich Materials Science), Cell Press
BM1.3: Responsive Materials
Tuesday AM, November 29, 2016
Hynes, Level 1, Room 102
9:30 AM - *BM1.3.01
From Nano to Micro and Back—Porphyrin Supramolecular Assembly for Cancer Imaging and Therapy
Gang Zheng 1 2
1 Department of Medical Biophysics University of Toronto Toronto Canada, 2 Princess Margaret Cancer Centre Toronto CanadaShow Abstract
Porphyrins are aromatic, organic, light-absorbing molecules that occur abundantly in nature, especially in the form of molecular self-assemblies. In 2011, we first discovered ‘porphysomes’, the self-assembled porphyrin-lipid nanoparticles with intrinsic multimodal photonic properties. The high-density porphyrin packing in bilayers enables the absorption and conversion of light energy to heat with extremely high efficiency, making them ideal candidates for photothermal therapy and photoacoustic imaging. Upon nanostructure dissociation, fluorescence and photodynamic activity of porphyrin monomers are restored. In addition, metal ions can be directly incorporated into the porphyrin building blocks of the preformed porphysomes thus unlocking their potential for PET and MRI. By changing the way porphyrin-lipid assembles, we developed HDL-like porphyrin nanoparticles (<20nm), porphyrin microbubbles (~2um), giant porphyrin vesicle (~100um) and hybrid porphyrin-gold nanoparticles, expanding the purview of porphyrin nanophotonics. By mimicking light harvest systems in photosynthetic bacteria, we introduced high-ordered porphyrin aggregates into supramolecular assemblies, resulting unprecedented photonic properties (e.g., reversible photoacoustic nanosensors). Such optical properties are also responsible for our discovery of the ultrasound-induced microbubbles-to-nanoparticle conversion phenomenon, which may open the door to bypass the enhanced permeability and retention effect when delivering drugs to tumors. By closing the nano-micro-nano loop, the simple yet intrinsic multimodal nature of porphyrin self-assembly represents a new frontier in cancer imaging and therapy.
10:00 AM - *BM1.3.02
From Filomicelles to 'Self' Recognition
Dennis Discher 1
1 University of Pennsylvania Philadelphia United StatesShow Abstract
Drug carriers have traditionally been spherical and designed to be more difficult to clear by using synthetic polymers that are hydrophilic such as PEG. We have explored filamentous shapes and also 'Self' signaling by peptides rather than PEG in various efforts to advance delivery science. In the first example (1), we sought to improve the delivery of aromatic drugs using micelles, particularly elongated filomicelles, and to that end aromatic groups were integrated into the hydrophobic block of a degradable di-block copolymer. These aromatic filomicelles were formed by self-directed assembly of amphiphilic di-block copolymer PEG-PBCL with suitable block ratios. Long and flexible worm-like micelles with an aromatic core were loaded with a common chemotherapeutic, Paclitaxel, for tests of release as well as effects on cancer cell lines in vitro and in vivo. For carcinoma lines in vitro and initial tests in vivo, flexible filomicelles with an aromatic core form an efficient drug delivery system that leads to higher cell death than previously reported systems, while inducing aneuploidy in surviving cells. In the second example, we explore better biomimickry with a 'Self' polypeptide. ‘Self’ cells are spared due to a polypeptide found on all cells that marks cells as ‘Self’, limiting their phagocytic clearance in vitro and in vivo – even when displayed on nanoparticles (2). Application to nanoparticle-based tumor imaging will be illustrated, as will application of the pathway to a cell-based therapy for cancer that exploits the ability of phagocytic cells to deeply penetrate into disease sites such as tumors.
(1) P.R. Nair, K. S. Anbazhagan, K.R. Spinler, M.R. Vakili A. Lavasanifar, and D.E. Discher. Filomicelles from aromatic di-block copolymers increase paclitaxel-induced tumor cell death and aneuploidy compared to aliphatic copolymer. Nanomedicine (May/June 2016).
(2) Rodriguez, P.L.; Harada, T.; Christian, D.A.; Pantano, D.A.; Tsai, R.K.; and Discher, D.E. Minimal 'Self' peptides that inhibit phagocytic clearance and enhance delivery of nanoparticles. Science 2013 339: 971-975
10:30 AM - *BM1.3.03
Target-Enabled In Situ Ligand Assembly (TESLA) for Molecular Imaging Applications
Jianghong Rao 1
1 Stanford University Palo Alto United StatesShow Abstract
Molecules or materials that can undergo property changes upon stimulation by a specific biological target promise a myriad of biomedical applications. We have been interested in a molecular ligand scaffold that can undergo in situ assembly, ideally even in the complex in vivo settings, after the activation by a specific molecular target. This assembling process would transform small ligands to large molecular complexes even nanoparticles at the target-presenting location. We envision that such systems can then be applied to in vivo imaging of the target activity and drug delivery. There are many reported examples of these small ligand assemblies, however, few could take place in vivo. This presentation will introduce our effort in developing such a molecular ligand scaffold for in vivo molecular imaging. We call it Target-Enabled in Situ Ligand Assembly (TESLA).
Our TESLA platform is based on a biocompatible chemical condensation reaction between two chemical groups -- 1,2-aminothiol and 2-cyanobenzothiazole. TESLA ligands possess both groups and upon the activation by the target, TESLA ligands will chemically condense, followed by assembly and formation of nanoparticles. Several TESLA ligands have been designed to validate the strategy in vitro, in living cells under the control of pH, disulfide reduction and/or enzymatic cleavage. Importantly, this TESLA platform is also working in living animals, and I will describe examples of TESLA probes in image treatment-induced apoptosis in tumor cells in vivo with whole-body fluorescence imaging, positron emission tomography (PET), and magnetic resonance imaging (MRI). We expect more TESLA probes may be designed to image many molecular targets and enable medical applications beyond imaging.
11:30 AM - *BM1.3.04
Soft Functional Actuators—Biomemetics and Materials
George Whitesides 1
1 Department of Chemistry and Chemical Biology Harvard University Cambridge United StatesShow Abstract
Biology offers an endless variety of functional solutions to motion, sensing, and control. This talk will summarize parts of a program focused on biomimetic and biostimulated soft actuators.
12:00 PM - *BM1.3.05
Fuel-Driven Active Materials
Jan van Esch 1 , Wouter Hendriksen 1 , R. Eelkema 1 , G. Koper 1
1 Department of Chemical Engineering Delft University of Technology Delft NetherlandsShow Abstract
It remains a huge scientific challenge to understand and mimic the utilisation of chemical energy in
biological systems to achieve the highly adaptable organisation and sophisticated functions like
active transport, motility, self-repair, replication, and adaptability. The development of biomimetic
systems with similar energy consuming organisation and functions requires a radical departure
from equilibrium self-assembly approaches, towards out-of-equilibrium systems driven by the
continuous input of energy.
In our research we focus on the development of active materials driven by chemicals fuels. First, I
will discuss how active materials can result from the transient self-assembly of synthetic molecules,
driven by the consumption of a chemical fuel. In these materials, reaction rates and fuel levels,
instead of equilibrium composition, determine properties such as lifetime, stiffness, and selfregeneration
capability. Then, I will discuss our recent steps to achieve temporal and spatial over
fuel-driven self-assembly by the development of a chemical reaction network that allow for
feedback control. Such systems will form the basis for self-organising systems and for design and
construction of energy-consuming dynamic devices and materials.
 J. Boekhoven, A.M. Brizard, K.N. Kowlgi, G.J. Koper, R. Eelkema, J.H. van Esch, Angew. Chem. Int. Ed. 2010, 49
 J. Boekhoven, W. Hendriksen, G. Koper, R. Eelkema, J.H. van Esch, Science 2015, 349, 1075.
 A.G.L. Olive, N. Hakimin Abdullah, I. Ziemecka, E. Mendes, R. Eelkema, J.H. van Esch, Angew. Chem. Int. Ed. 2014,
12:30 PM - *BM1.3.06
Sankaran Thayumanavan 1
1 University of Massachusetts Amherst United StatesShow Abstract
Molecular designs that afford tunable supramolecular assemblies are of interest in a variety of applications, including drug delivery, sensing, and diagnostics. When these assemblies are nanoscopic in size and are responsive to specific stimulus, then the interests in these nanoscale scaffolds are even higher. We have developed amphiphilic supramolecular assemblies featuring these characteristics. In addition, these assemblies also can bind guest molecules efficiently and release them in response to specific triggers. Our utlimate goal is to develop design algorithms that lend themselves to predictably design nanoscale assembleis that respond to physical, chemical, or biological stimuli. Fundamental and translational implications of these findings would be numerous. We will report our progress in this area.
BM1.4: Materials for Medicine
Tuesday PM, November 29, 2016
Hynes, Level 1, Room 102
2:30 PM - *BM1.4.01
Translational Anticancer Nanomedicines through Controlled Chemistry
Jianjun Cheng 1 , Hua Wang 2
1 University of Illinois at Urbana-Champaign Urbana United States, 2 Harvard University Cambridge United StatesShow Abstract
Nanomedicine has offered new solutions for cancer diagnosis and therapy. However, the survival improvement offered by current nanomedicines remains modest. To further advance the development of nanomedicines, it is crucial to investigate and understand the correlation between the properties of nanomedicines (e.g., particle size) and biological responses to lay the foundation for the design of next-generation nanomedicines with optimum efficacy against cancers. Here, we report the development of size-controlled, monodisperse drug-silica nanoconjugates and systematically evaluation of their size effect on antitumor efficacy in both primary and metastatic tumor models. We find that the 50-nm nanoconjugate has the most optimal antitumor efficacy compared to 200- and 20-nm nanoconjugates. The silica-drug nanoconjugates show great potential for clinical applications because of their long-term biocompatibility and their capability of in vivo clearance. I will also present our recent progress of developing polymeric nanoparticles for cancer treatment.
3:00 PM - *BM1.4.02
Role of Nanoparticle Morphology in Crossing Biological Barriers
Samir Mitragotri 1
1 University of California, Santa Barbara Santa Barbara United StatesShow Abstract
Nanoparticles find intriguing applications in drug delivery. The morphological properties of nanoparticles can greatly impact their ability to cross biological barriers such as cell membranes, intestinal epithelium, blood brain barrier and vascular endothelium. Several recent studies, including our own, have outlined the role of particle morphology in their transport across these barriers and these studies have shown that particle morphology can indeed significantly alter their transport. In many cases, morphology operates in synergy with other parameters such as size and surface chemistry to bring out unique interplay between these key parameters. My talk will present an overview of the current understanding of the role of particle morphology in crossing these varied barriers and lessons learned about the similarity and differences in the role of particle morphology in determining delivery across the barriers.
3:30 PM - *BM1.4.03
Artificial Spores—Cytocompatible Nanoencapsulation of Individual Living Cells
Insung Choi 1
1 KAIST Daejeon Korea (the Republic of)Show Abstract
Nature has developed a fascinating strategy of cryptobiosis (“secret life”) for counteracting the stressful, and often lethal, environmental conditions that fluctuate sporadically over time. For example, certain bacteria sporulate to transform from a metabolically active, vegetative state to an ametabolic endospore state. The bacterial endospores, encased within tough biomolecular shells, withstand the extremes of harmful stressors, such as radiation, desiccation, and malnutrition, for extended periods of time and return to a vegetative state by breaking their protective shells apart when their environment becomes hospitable for living. Certain ciliates and even higher organisms, e.g., tardigrades, and others are also found to adopt a cryptobiotic strategy for their survival. A common feature of cryptobiosis is the structural presence of tough sheaths on cellular structures. However, most cells and cellular assemblies are not “spore-forming” and vulnerable to the outside threats. In particular, mammalian cells, enclosed with labile lipid bilayers, are highly susceptible to in vitro conditions in the laboratory and daily-life settings, making manipulation and preservation difficult outside of specialized conditions. The instability of living cells has been a main bottleneck to the advanced development of cell-based applications, such as cell therapy and cell-based sensors.
Recent studies have sought to chemically control and tailor the metabolic behaviors of non-spore-forming cells, as well as enhancing their viability against adverse environmental conditions, by forming thin (< 100 nm), tough artificial shells. These living “cell-in-shell” structures, called artificial spores (chemically-formed spore-like structures), enable control of cell division, protection against physical and chemical stresses, and cell-surface functionalizability, as well as providing the cells with exogenous properties that are not innate to the cells but are introduced chemically, such as magnetism, heat-tolerance, and UV-resistance. In addition, recent developments in the field have further advanced the synthetic tools available to the stage of chemical sporulation and germination of mammalian cells, where cytoprotective shells are formed on labile mammalian cells and broken apart on demand. Based on these demonstrations, the (degradable) cell-in-shell hybrids are anticipated to find their applications in various biomedical and bionanotechnological areas, such as cytotherapeutics, high-throughput screening, sensors, and biocatalysis, as well as providing a versatile research platform for single-cell biology.
4:30 PM - *BM1.4.04
Nanolayered Staged Delivery Approaches to Trauma Treatment and Wound Healing
Paula Hammond 2 1
2 Department of Chemical Engineering Massachusetts Institute of Technology Cambridge United States, 1 Koch Institute of Integrative Cancer Research Massachusetts Institute of Technology Cambridge United StatesShow Abstract
The use of alternating layer-by-layer (LbL) assembly enables a modular platform that can control release of therapeutics over a broad range of time scales, from several seconds to multiple months. We have developed systems that can address a range of different wound healing needs by taking advantage of this tunable platform and the ability to incorporate drugs programmed to release at a range of different rates and with staged release behavior. The nature of the layering process enables the incorporation of different drugs within different regions of the thin film architecture; the result is an ability to uniquely tailor both the independent release profiles of different therapeutics from the same film, and the order of release of molecules to targeted regions of the body.
This approach can be used to assemble thrombin protein and self-assembling peptides in a dry film conformal coating on a fully resorbable sponge to engage rapid hemostasis over a period of seconds to minutes; these systems can be stored for extended time periods in medical facilities, thus allowing rapid deployment by medical staff and a means of introducing more effective hemostasis for cases of internal bleeding and hemorrhage. The addition of the co-release of anti-infective agents such as vancomycin to these systems adds additional value to the soldier by preventing infection across a broad spectrum, which is particularly relevant on the battlefield. On the other hand, staging of release of multiple growth factor proteins can achieve the regeneration of collagen and remodeling of tissue in wounds at appropriate time points to facilitate wound closure and tissue vascularization. Moreover, multilayered release coatings as thin as a half micron to several microns can be designed to deliver different growth factor proteins or siRNA and other biologic drugs directly to wounds to correct the dysregulation of wound healing processes that have gone awry, from burn and scar tissue to the closure of chronic wounds such as diabetic ulcers.
5:00 PM - *BM1.4.05
A Powerful CD8+ T-Cell Stimulating D-Tetra-Peptide Hydrogel as a Very Promising Vaccine Adjuvant
Huaimin Wang 1 , Chengbiao Yang 1 , Zhimou Yang 1
1 Nankai University Tianjin ChinaShow Abstract
Subunit vaccines are well-defined at molecular level and have been widely developed in modern vaccine industry due to their good safety, great ease of manufacture and storage. However, compared with live vaccines, their immunogenicity is poor, particularly for the CD8+ T-cell responses. Subunit vaccines and adjuvants have therefore been formulated into nanomaterials to raise immune responses, but only few of them can elicit CD8+ T-cell responses. More importantly, the antigens and adjuvants are needed to be covalently conjugated or simultaneously formulated into the same nano-carrier, which makes their production in large scale more challenging. We had developed an injectable supramolecular hydrogel of a self-assembling D-tetrapeptide as a very promising adjuvant to raise both humoral and cellular immune responses. Antigens including OVA and attenuated tumor cells can be simply incorporated within the hydrogel by vortex or gentle shaking before injections. We found that the resulting hydrogels with physically entrapped antigens are extremely potent vaccines that can significantly stimulate CD8+ T-cell response and remarkably inhibited tumor growth. Our hydrogel should enable a wide range of subunit vaccines and make the manufacture of modern vaccines much easier.
Zichao Luo, Qinjie Wu, Chengbiao Yang, Huaimin Wang, Tao He, Hao Chen, Xingyi Li,* Changyang Gong*, Zhimou Yang* A powerful CD8+ T-cell stimulating D-tetra-peptide hydrogel as a very promising vaccine adjuvant, Adv. Mater. Under Revision.
Huaimin Wang，Zichao Luo，Youzhi Wang，Tao He，Chengbiao Yang，Chunhua Ren，Linsha Ma，Changyang Gong*，Xingyi Li*，Zhimou Yang*，Enzyme-catalyzed Formation of Supramolecular Hydrogels as Promising Vaccine Adjuvants，Adv. Funct. Mater., 2016, 26(11): 1822-1829.
Yue Tian, Huaimin Wang, Ye Liu, Lina Mao, Wenwen Chen, Zhening Zhu, Wenwen Liu, Wenfu Zheng, Yuyun Zhao, Deling Kong, Zhimou Yang*, Wei Zhang, Yiming Shao*, Xingyu Jiang*, A Peptide-based Nanofibrous Hydrogel as a Promising DNA Nanovector for Optimizing the Efficacy of HIV Vaccine, Nano Lett., 2014, 14(3): 1439-1445.
5:30 PM - *BM1.4.06
Inverse Opal Scaffolds for Tissue Engineering and Regenerative Medicine
Younan Xia 1
1 Georgia Institute of Technology Atlanta United StatesShow Abstract
Three-dimensionally porous scaffolds are indispensable for tissue engineering and regenerative medicine as they provide physical supports and adjustable microenvironments for cells to attach, stretch, migrate, proliferate, and differentiate. An ideal scaffold should possess certain properties such as appropriate pore size, porosity, and interconnectivity, among others. To this end, porous scaffolds with an inverse opal structure emerged. Unlike other scaffolds that are fabricated by stochastic porogen methods with random structures, an inverse opal scaffold is characterized by uniform and well-controlled pores and interconnecting windows, in addition to their highly reproducible structure among different batches of production. In this talk, I will start with a biref discussion of the motivation for developing the inverse opal scaffolds and an introduction to the fabrication method. I will then highlight the advantages of using such porous scaffolds over their counterparts with non-uniform structures through side-by-side comparisons. Finally, I will discuss a few examples on the unique applications of the inverse opal scaffolds in regenerative medicine and offer some perspectives on the future directions.
Bing Xu, Brandeis University
Shawn Chen, National Institute of Biomedical Imaging and Bioengineering
Honggang Cui, The Johns Hopkins University
Brandeis University, MRSEC, MilliporeSigma (Sigma-Aldrich Materials Science), Cell Press
Wednesday AM, November 30, 2016
Hynes, Level 1, Room 102
9:30 AM - *BM1.5.01
Structure and Function of Hydrogels Comprising Self-Sorted Supramoleular Fibers
Itaru Hamachi 1 2
1 Kyoto University Kyoto Japan, 2 CREST/JST Tokyo JapanShow Abstract
Self-sorting event is ubiquitous in living systemrs and it should be one of the crucial factors for their dynamic and flexible functions. Therefore, it is recently considered that self-sorted supramolecular assemblies such as supramolecular nanofibers are invaluable for complex but well-organized systems with sophisticated functions like living cells. To design and control the self-sorting events in synthetic materials, understanding their structures and dynamics in detail is indispensable. I herein describe in situ real-time imaging of self-sorted supramolecular nanofibers consisting of a peptide gelator and an amphiphilic phosphate gelator by using confocal laser scanning microscopy and super resolution imaging. Design and selection of orthogonal supramolecular fibers and appropriate fluorescent probes allowed us to visualize the self-sorted fibers entangled in 2D and 3D in the hydrogel state with 80 nm resolution. In situ time-lapse imaging unveiled that the physicochemical properties remained intact in the orthogonal fibers and that there is a remarkable difference in the fiber formation rate between the two fibers. Moreover, we are able to directly visualize the stochastic non-synchronous fiber formation with the cooperative mechanism in real-time, which cannot be detected by conventional techniques. I would also like to discuss the function of supramolecular hydrogels made of such self-sorted fibers.
10:00 AM - *BM1.5.02
A Multi-Phase Transitioning Peptide Hydrogel for Suturing Ultra-Small Vessels
Joel Schneider 1
1 National Cancer Institute Frederick United StatesShow Abstract
Reconstructive, cardiac, vascular, and transplant surgeries rely heavily on the anastomosis of venous and arterial vessels. However, traditional suturing techniques have an increased rate of failure as the size of the vessels decrease. Millimeter-sized vessels are difficult even for experienced surgeons and anastomosing micron-sized vessels is barely possible with conventional microsurgical techniques. Herein, we report the design of a peptide-based hydrogel capable of undergoing multiple consecutive phase transitions enabling its use as an injectable temporary intraluminal stent during micron-scale anastomosis. The peptide (APC1) undergoes an initial sol-gel phase transition under physiological conditions to form a self-supporting hydrogel directly in a syringe. The resultant gel demonstrates shear-thin/recovery rheological properties that allow its syringe delivery directly into the lumen of collapsed vessels re- establishing their shape and providing mechanical support. The transparent gel can also be applied to the interspace between vessel ends, providing a flexible medium into which the vessels can be inserted, physically manipulated, but temporally fixed after placement, allowing clamp-free approximation with minimal lumina handling. Suturing is performed directly through the shear-thinning gel medium. On completion, gel applied external to the vessel is washed away. The final gel- from the vessel interior is enabled by the incorporation of a photo-caged amino acid, 4-methoxy-7-nitroindolinyl glutamic acid [E(MNI)], into the primary peptide sequence. Irradiation of the material with 365 nm light de-cages the residue and disrupts the hydrogel network allowing the resumption of blood flow. Biophysical and in-vivo experiments show that this responsive hydrogel has the potential to decrease the surgical difficulty associated with anastomosing ultra-small vessels, adding a new tool to the armamentarium for micro- and supermicrosurgical procedures.
10:30 AM - *BM1.5.03
Dynamic Peptide-DNA Materials
Samuel Stupp 1
1 Northwestern University Evanston United StatesShow Abstract
Supramolecular assemblies, biopolymers, and proteins found in extracellular matrices and in the cytosol control many functions of the cell in a highly dynamic fashion. The assemblies commonly take the form of supramolecular polymers formed by protein monomers. Another important family of biopolymers includes charged polysaccharides with complex and aperiodic sequences that can bind many proteins. The highly dynamic structures serve as scaffolds for biological signals and mediators of fundamental processes such as cell division and migration. This lecture will describe the development of a novel synthetic platform of materials that enables the temporal switching of signals presented to cells in order to control their behavior. The new biomaterials are constructed with DNA and peptide nucleic acids conjugated to peptides. Using these systems we have observed reversible migration of neural stem cells and also reversible biological attachment of cells to substrates. A second platform to be described in this lecture involves the use of glycopeptide filaments with capacity for multipotent activation of signaling proteins. The lecture will discuss the importance of these two emerging platforms in regenerative medicine.
11:30 AM - *BM1.5.04
Dynamic Peptide Libraries for Discovery of Supramolecular Nanomaterials
Rein Ulijn 1
1 The City University of New York Glasgow United KingdomShow Abstract
The tremendous functionality of living systems is based on sequence-specific polymers and it is increasingly clear that much simpler oligomers, such as peptides, are suitable building blocks for supramolecular nanomaterials with myriad applications. However, the design and selection of self-assembling sequences is challenging due to the vast combinatorial space available. In this take, we will present our recently developed methodology that enables the peptide sequence space to be searched for self-assembling structures. In this approach, unprotected homo- and hetero dipeptides including aromatic, aliphatic, polar and charged amino acids are subjected to continuous enzymatic condensation, hydrolysis and sequence exchange to create a dynamic combinatorial peptide library. The free energy change associated with the assembly process itself giving rise to selective amplification of self-assembling candidates. By changing the environmental conditions during the selection process, different sequences and consequent nanoscale morphologies are selected. Thus, dynamic peptide libraries enable directed discovery of peptide nanomaterials under user-defined conditions. Applications in discovery of theranostic peptide nanoparticles for cancer therapeutics will be discussed.
12:00 PM - *BM1.5.05
Synthesis, Design, and Assembly of Spatiotemporally-Controlled Hyaluronan Hydrogels
Molly Shoichet 1 , Stephanie Fisher 1 , Alexander Baker 1 , Roger Tam 1 , Laura Smith 1
1 Department of Chemical Engineering and Applied Chemistry University of Toronto Toronto CanadaShow Abstract
Biomimetic, three-dimensional cell culture opens the opportunity to both improve our understanding of disease progression and achieve more predictive drug screening. We have designed a series of crosslinked hydrogels based on hyaluronan, a naturally occurring polysaccharide that makes up the extracellular matrix of cells throughout the body. Hyaluronan is upregulated in breast and other cancers and is often a marker for breast cancer, making it an excellent biomaterial in which to design other key biomimetic properties. To gain greater insight into the factors that influence cell migration in breast and brain cancer, we have designed Diels-Alder crosslinked hyaluronan hydrogels where mechanical and chemical properties are independently controlled, thereby providing insight into why some of the key factors of the extracellular matrix that influences cell migration. Since glioblastoma is an invasive cancer and breast cancer cells migrate to other sites, the role of the extracellular matrix and other cell types on these biological phenomena can help us understand disease progression. To gain greater insight into cell fate when exposed chemotherapeutic drugs, we have synthesized aldehyde-crosslinked hyaluronan hydrogels where the chemistry allows the cells to be cultured in a 3D environment. Here the cellular response to chemotherapeutic drugs can be explored and compared to those observed when cells are cultured in 2D or in the standard Matrigel. A key advantage of the these hyaluronan-based hydrogels is their well-defined chemistry and reproducibility, a key limiting affect of Matrigel.
12:30 PM - *BM1.5.06
Intracellular Self-Assembly of a Low-Molecular-Weight Gelator Induces Selective Death of Cancer Cells
Tatsuo Maruyama 1 , Akiko Tanaka 1
1 Kobe University Kobe JapanShow Abstract
Low-molecular-weight hydrogels have attracted attention as a functional soft material for a variety of applications (tissue engineering, DDS carriers and cell cultivation). The low-molecular-weight gelators can be designed to self-assemble in response to various stimuli owing to their variability of the molecular structures. In particular, enzyme-responsive low-molecular-weight gelators have high potential in the biochemical and medical applications. Here we report a peptide-lipid low-molecular-weight gelator designed to transform from a gelator precursor to a gelator by a cancer-related enzyme. The transformation was mediated by a proteolytic enzyme, matrix metalloproteinase-7 (MMP-7) that was secreted by cancer cells, resulting in the gelation. We anticipated that the gelation by a low-molecular-weight gelator inside or around cancer cells would affect the low-molecular-weight gelator of cancer cells. In the present study, we succeeded in the uptake of the low-molecular-weight gelator and also in the gelation of cytoplasm of cancer cells, inducing the selective death of cancer cells based on the intracellular self-assembly of our low-molecular-weight gelator.
The gelator precursor consisted of three moieties, a low-molecular-weight gelator, an enzyme-cleavage site and a gelation-preventing moiety. The properties of the gelator precursor were evaluated by transmission electron microscopy, gelation test and HPLC analysis. These investigations revealed that the hydrolysis of the gelator precursor by MMP-7 produced the gelator molecules, which self-assembled to form entangled nanofibres, resulting in the gelation of an aqueous phase.
To investigate the cytotoxicity of the gelator precursor, the gelator precursor was added to cultures of the mammalian cells. The gelator precursor had cytotoxicity to HeLa cells (cancer cells) but not to normal cells. The cytotoxicity was correlated with the amount of MMPs secreted by cells.
To explore the mechanism of the cancer-cell death, a gelator analogue containing a fluorophore was added to the cell culture with the gelator precursor. The fluorescence microscope observation revealed the cell uptake of the gelator and the low fluidity of the cell interior, suggesting the gel-like structure inside a cell. This study proposes that the molecular self-assembly inside cancer cells can be available as a novel strategy for developing a novel anti-cancer drug.
BM1.6: Emerging Leaders
Wednesday PM, November 30, 2016
Hynes, Level 1, Room 102
2:30 PM - *BM1.6.01
Small and Bright—Functional Luminescent Nanoparticles for Bioimaging and Optogenetic Applications
Gang Han 1
1 Medical School University of Massachusetts Worcester United StatesShow Abstract
Functional luminescent nanoparticles are promising materials for in vitro and in vivo optical imaging and therapy due to their unique optical and chemical properties. In this talk, I will present two new types of biocompatible luminescence nanoparticles. The first type of materials is upconversion nanoparticles (UCNPs). They absorb low energy near-infrared (NIR) light and emit high-energy shorter wavelength photons. Their special features allow them to overcome various problems associated with conventional imaging probe at both single molecule and ensemble levels. I will present new developments regarding engineering UCNPs towards deep tissue imaging, photodynamic therapy, optogenetic applications in neuroscience and immunotherapy. The second type of nanoparticles is persistent luminescence nanoparticles (PLNPs). They are bioluminescence-like and possess unprecedented in vivo deep tissue energy rechargeability, outstanding signal-to-noise-ratio with no need for an excitation resource (light) during imaging, and they can be directly detected with existing imaging systems. These nanoparticles continue to emit light for minutes or hours and, in some cases, days, after turning off the excitation source. These long-lasting, light-emitting nanocrystals can provide noninvasive imaging technology for evaluating structural and functional biological processes in living animals and patients.
3:00 PM - *BM1.6.02
Overcoming the Intrinsic Biopharmaceutical Difficulties of Oligonucleotides and Chemotherapeutics with Their Combination
Ke Zhang 1
1 Northeastern University Boston United StatesShow Abstract
Nucleic acids are generally regarded as the payload molecule in gene therapy, requiring a carrier for intracellular delivery. Given the recent discovery that spherical nucleic acids enter cells rapidly compared to their linear counterpart, however, nucleic acids also have the potential to function as a delivery vehicle. We report a strategy where the nucleic acid component acts as both a payload for intracellular gene regulation and the delivery vehicle for the drug component. A bioreductively activated, self-immolative disulfide linker is used to tether the drug, allowing free drug to be released upon cell uptake. We found that the DNA-drug nanostructures enter cells ca. 100 times faster than free DNA, exhibit increased stability against nuclease, and show nearly identical cytotoxicity as free drug toward cancer cells. These DNA-drug nanostructures allow one to separately access a gene target and a drug target using only the payloads themselves, bypassing the need for a complex co-carrier system.
4:30 PM - *BM1.6.03
Self-Assembly of Hybrid Assemblies for Cancer Imaging and Therapy
Zhihong Nie 1
1 University of Maryland College Park United StatesShow Abstract
Cancer is the second leading cause of death in the United States, next only to heart disease. More effective diagnostic and therapeutic strategies are in urgent need for better management of patients with cancers. Both inorganic and organic (or polymeric) nanoparticles (NPs) have been widely explored for therapeutic and diagnostic applications. Among others, inorganic NPs are attractive for the treatment, diagnosis, and detection of tumors, because of their unique features as compared with their organic and polymeric counterparts. For example, the surface plasmonic resonance and photothermal effect of Au NPs leverage their functions in simultaneous cancer imaging such as photothermal and photoacoustic imaging, as well as photothermal ablation of tumors. The response of magnetic NPs to magnetic fields enables their contrast-enhanced magnetic resonance imaging (MR) imaging and targeted delivery of therapeutic agents. For this purpose, single NPs are often used and functionalized with organic or polymeric ligands to improve their stability, biocompatibility and functionality.
While single NPs are attractive, the self-assembly of NPs can yield materials with new or advanced properties that are different from their individuals. For example, the organization of Au NPs allows for tuning the absorption of NP ensembles in the near-infrared (NIR) window which is highly desired for in vivo applications. The clustering of magnetic NPs within micelles dramatically increases the MR imaging contrast and responsiveness to external magnetic field. It is, therefore, expected that the ability to design assembled structures with tailored spatial arrangement of NPs may facilitate the utilization of inorganic NPs in biomedical applications. In this talk, I will present our efforts to develop new strategies for the self-assembly of polymer-functionalized inorganic NPs into functional hybrid materials and to evaluate the hybrid assemblies for cancer imaging and treatment. Specifically, I will introduce i) the molecular or atomic mimicking assembly of gold and magnetic NPs into a diverse range of complex nanoarchitectures; and ii) the utilization of hybrid assemblies, particularly vesicular structures containing gold NPs, magnetic NPs or both for effective multimodality cancer imaging (i.e., photothermal, photoacoustic, and MR imaging) and combinational cancer therapy (i.e., photothermal ablation of tumor, photodynamic therapy, and targeted delivery-based chemotherapy).
5:00 PM - BM1.6.04
Nanomaterial Mimicry of the Metastatic Niche
Daniel Heller 1 2
1 Memorial Sloan-Kettering Cancer Center New York United States, 2 Weill Cornell Medical College New York United StatesShow Abstract
Disseminated tumors are poorly accessible to nanoscale drug delivery systems due to the vascular barrier, which attenuates extravasation at the tumor site. P-selectin, a molecule expressed on activated vasculature, facilitates metastasis by arresting tumor cells at the endothelium. We explored a nanomaterials solution to use P-selectin as a potential target for drugs to reach the same tumors that it helps to create. To develop a targeted drug delivery platform, we synthesized nanoparticles incorporating a fucosylated polysaccharide with nanomolar affinity to P-selectin. We studied the ability of these nanoparticles to target P-selectin and consequently arrest at the tumor vasculature.
The nanoparticles targeted the tumor microenvironment to localize chemotherapeutics and a targeted therapeutic drugs at tumor sites in both primary and metastatic models, resulting in superior anti-tumor efficacy. On tumors devoid of P-selectin, we found that ionizing radiation guided the nanoparticles to the disease site by inducing P-selectin expression. Radiation concomitantly produced an abscopal-like phenomenon wherein P-selectin appeared in unirradiated tumor vasculature, suggesting a potential strategy to target disparate drug classes to almost any tumor.
5:15 PM - BM1.6.05
3D Printing of Alginate Microstructures with Tunable Degradation Kinetics
Thomas Valentin 1 , Po-Yen Chen 1 , Jaskiranjeet Sodhi 1 , Susan Leggett 1 , Hayley Mcclintock 1 , Ian Wong 1
1 Brown University Providence United StatesShow Abstract
3D printing is a promising approach for designer biomaterial architectures with information-rich structure and dynamic functionality. In particular, stimuli-responsive hydrogels consisting of crosslinked, hydrophilic polymers could be used for tissue engineering, drug delivery and other biomedical applications. One design consideration is that these biomaterials must be responsive to at least two physicochemical stimuli – the first to pattern desired structures and additional orthogonal stimuli to trigger dynamic behaviors such as degradation. Here, we show reversible 3D printing of alginate hydrogel microstructures using stereolithography (SLA) and subsequent degradation using ion chelation. Alginate is crosslinked by divalent cations, which can be generated by selective illumination of photoacid generators (PAG) in the presence of insoluble salts with these cations. We systematically explore how hydrogel degradation kinetics, pattern fidelity and mechanical properties depend on the concentration and composition of divalent cations in the precursor solution. We use degradable 3D printed alginate structures as “obstacle courses” to investigate collective epithelial migration in confined geometries. We envision other applications in 3D biofabrication of soft robots, organs on chips and other bioinspired microdevices.
5:30 PM - BM1.6.06
Supramolecular Biomaterials—From Fundamentals to Advanced Healthcare Solutions
Eric Appel 1
1 Department of Materials Science amp; Engineering Stanford University Stanford United StatesShow Abstract
Hydrogels are an important class of biomaterial that have received much attention for tissue engineering and controlled drug-delivery applications on account of their similarity to soft biological tissue and highly tunable mechanical properties. Supramolecular hydrogels are dynamically cross-linked polymer networks exhibiting viscous flow under shear stress (shear-thinning) and rapid recovery of mechanical properties when the applied stress is relaxed (self-healing). These properties afford minimally invasive implantation in vivo though direct injection or catheter delivery to tissues, contributing to a rapid gain in interest in their application for drug delivery and tissue engineering. Herein, we discuss the preparation and application of shear-thinning, injectable hydrogels driven by non-covalent interactions between modified biopolymers (BPs) and biodegradable nanoparticles (NPs) comprised of poly(ethylene glycol)-block-poly(lactic acid) (PEG-b-PLA). Owing to the non-covalent interactions between PEG-b-PLA NPs and BPs, the hydrogels flow under applied stress and their mechanical properties recover completely within seconds when the stress is relaxed, demonstrating the shear-thinning and injectable nature of the material. Moreover, the hierarchical construction of these biphasic hydrogels allows for multiple therapeutic compounds to be entrapped simultaneously and delivered with differential release profiles in vitro and in vivo. Delivery of the loaded therapeutics is controlled both by Fickian diffusion from the hydrogel and erosion-based release from the gel surface and can be tuned over several months, enabling novel long-term treatment strategies for chronic diseases. Furthermore, their mild formation and unique flow properties allow for facile encapsulation and implantation of thereapeutically-relevant cells with enhanced viability and retention within the implantation site. Overall, this presentation will demonstrate the facile synthesis of an injectable hydrogel affording minimally invasive application in vivo and controlled release of therapeutics and therapeutic cells.
5:45 PM - BM1.6.07
Programming Immune Tolerance Using Quantum Dots to Control Self-Antigen Display
Christopher Jewell 1 2 3
1 Fischell Department of Bioengineering University of Maryland, College Park College Park United States, 2 Department of Microbiology and Immunology University of Maryland School of Medicine Baltimore United States, 3 Tumor Immunology and Immunotherapy Program Marlene and Stewart Greenebaum Cancer Center Baltimore United StatesShow Abstract
Multiple sclerosis (MS) and other autoimmune diseases occur when the immune system incorrectly attacks self-molecules. In MS, for example, the immune system attacks myelin – a matrix that insulates neurons in the brain. The effects of this attack are devastating, degrading patient motor function until even simple tasks are impossible. Current treatments for autoimmunity are not curative and leave patients immunocompromised. For these reasons, new experimental therapies seek tolerance against specific self-antigens, without the broad suppression of current treatments. Responses toward self-antigens are generated in lymph nodes and the spleen, with the development of inflammation or tolerance influenced by the concentration and form of antigen reaching these sites. In particular, recent studies show that the configuration in which antigens are presented in lymph nodes can alter the processing of these ligands to activate natural regulatory pathways involved in tolerance. Thus efficient delivery of self-antigen to LNs with uniform, tunable control over peptide morphology or display density could enable more specific and effective therapies for autoimmune diseases. Toward this goal, we used simulation and experimental measurements to design nanocrystalline semiconductor quantum dots (QDs) that display dense arrangements of myelin self-peptides associated with disease in MS. These peptide-QD conjugates are uniform in size (<20 nm) and enable tunable display of 10-150 peptides per QD. In cell culture, this configurability allows direct control over the level of expansion of myelin-reactive T cells, while in mice, the conjugates are rapidly concentrated in draining lymph nodes; the intrinsic fluorescence of the QDs allows direct visualization of this process without addition of other components or fluorescent labels. During a pre-clinical mouse model of MS, treatment with peptide-QDs reduced disease incidence 10-fold and eliminated paralysis in mice. Strikingly, the degree of tolerance – and the underlying expansion of regulatory T cells measured in these mice – correlated with the density of myelin molecules installed and presented by the QDs. This is the first time QDs have been used to induce tolerance, creating new opportunities to study and combat autoimmunity by simultaneously controlling the display of peptide ligands in lymph node or other immunological tissues, while visualizing the trafficking and processing of these conjugates.
BM1.7: Poster Session I
Wednesday PM, November 30, 2016
Hynes, Level 1, Hall B
9:00 PM - BM1.7.01
Synthesis and Characterization of Bioinspired Dynamic Materials and Their Application in Oral Drugs Delivery
Saad Alshehri 1 , Tansir Ahamad 1
1 King Saud University Riyadh Saudi ArabiaShow Abstract
Macroporous natural dynamic materials (DM) were extracted from date palm (Phoenix dactylifera L.) and coated by natural polymers composite (carboxymethyl cellulose, polyvinyl alcohol and crosslinked by ethyleneglycol diglycidylether). The polymer coated bioinspired dynamic materials (PDM) were used in in-vitro investigations of controlled delivery of albandazol. DM, PDM and drugs loaded capsules (PDM-ALB) were characterized by scanning electron microscope (SEM), surface area (BET), Fourier-transform infrared (FT-IR), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The length of DM was found to be 20-20.5 mm and the pore sized was between 50-135 nm, as measured using SEM. The studies revealed that maximum loading of the drug is at pH 6.0 (97.2%, with 50 mg/ml,). The results indicate that by increasing the pH from 1.4 to 7.4, the cumulative release rates of albandazol in physiological buffer solution (PBS) is more than two times as in simulated gastric fluid (SGF). In addition, the in-vitro toxicity against Caco-2 cells was tested by the 3-[4,5-dimethylthiazole-2-yl]-2,5 diphenyltetrazolium bromide (MTT) assay, and the results showed that PDM are biocompatible materials. The overall results encourage continuing studies on the clinical use of PDM as drug carriers.
Keywords: Terpolymer, FTIR, activation energy, antimicrobial activity, metal complexes.
9:00 PM - BM1.7.02
Surface Enhanced Raman Spectroscopy in the Prescense of Hydroquinone Assisted by Gold Nanorods
Rodrigo Cabrera Alonso 1 , Francisco Javier Gonzalez Contreras 1
1 Coordination for the Innovation and Application of Science and Technology San Luis Potosí MexicoShow Abstract
In recent years there have been significant technological advances in the development of applications and electronic devices, on the other hand, there have been significant research in various areas such as medicine, optics, physics, chemistry, electronics, etc. Together both approaches, both scientific and technological, have converged in the development of new techniques for medical diagnosis. These new medical diagnostic techniques based on the use of the properties of light and the interaction of the same with biological samples are known as optical biopsy or, optical methods for non-invasive medical diagnosis. In particular, there are non-invasive analytical sciences to biomedical research in optical techniques. Which provide detailed information on the molecular composition, structure and interaction of the relationship between diseases and biochemical changes. One of the techniques most used today is Raman spectroscopy, which provides a "fingerprint" of the molecular structure of the sample that can be used to identify the material being analyzed.
However a disadvantage is that small amounts of clinically significant substances in biological samples beyond the detection limit of conventional Raman spectrometers, making them difficult or impossible to detect. Due to this low intensity in the Raman signal for biological samples, a variety of agents have been manufactured metal nanoparticles with unique optical properties for diagnostic and medical treatment. To perform Raman amplification of this signal, it is necessary to implement the technique known as surface enhanced Raman spectroscopy (SERS). Hydroquinone is a molecule of great interest because it is a substance found in skin lightening creams, which, when applied in high concentrations, it can be the cause of skin cancer. By means of Raman spectroscopy, a qualitative analysis for subsequent medical diagnosis is made.
9:00 PM - BM1.7.03
Novel Nanoprobes Optimized by Peptide Self-Assembly for Bioimaging Applications
Yanbin Cai 1 , Zhimou Yang 1
1 Nankai University Tianjin ChinaShow Abstract
The combination of an environment-sensitive fluorophore, 4-nitro-2,1,3-benzoxadiazole (NBD), and peptides have yielded supramolecular nanofibers with enhanced cellular uptake, brighter fluorescence, and significant fluorescence responses to external stimuli. We had designed and synthesized NBD-FFYEEGGH that can form supramolecular nanofibers and emit brighter than its counterpart of NBD-EEGGH without the self-assembling property. The nanofibers of NBD-FFYEEGGH could specifically bind to Cu2+, leading to the formation of fluorescence quenched elongated nanofibers. This fluorescence quenching property was enhanced in self-assembling nanofibers and could be applied for detection of Cu2+ in vitro and within cells. In a further step, an enzyme-cleavable DEVD peptide was placed between NBD-FFY and the copper binding tripeptide GGH. The resulting self-assembling peptide NBD-FFFDEVDGGH also showed strong fluorescence quenching to Cu 2+. Upon the enzymatic cleavage to remove the Cu2+-binding GGH tripeptide from the peptide, the fluorescence was restored. The cellular uptake of nanofibers was better than that of free molecules because of endocytosis. The supramolecular nanofibers with fluorescence turn-on property could therefore be applied for detection of caspase-3 activity in vitro and within cells. We believe that the combination of environment-sensitive fluorescence and fast responses of supramolecular nanostructures would lead to a useful platform to detect many important analytes.
Moreover,we had reported optimized ratiometric fluorescent probes by peptide self-assembly.The resulting self-assembled nanoprobes show extraordinary stability in aqueous solutions and extremely low background fluorescence in buffer solutions. Our optimized probes with much bigger ratiometric fluorescence ratios also show an enhanced cellular uptake, lower background noise, and much brighter fluorescence signal in the cell experiment. Our study provides a versatile and very useful strategy to design and produce fluorescent probes with better performance.
9:00 PM - BM1.7.04
Bioresponsive Conductive Polymer Based on Carbon Nanotube-Hydrogel Composites
Bo Wu 1 , Li-Jing Cheng 1 , Akash Kannegulla 1
1 Oregon State University Corvallis United StatesShow Abstract
Stimuli-responsive hydrogels have been used for chemical and biological sensing. Depending on the chemical side groups and moieties available on the hydrogel framework, the hydrogel undergoes a volume change in response to the presence of target stimuli, such as solution pH, temperature, and target biomolecules. The volume change of the hydrogel-based sensor is typically transduced into optical signals, including reflectance from hydrogel thin films, resonance spectra of hydrogel photonic crystals or direct measurement of volume change in microscope. The lack of direct electrical readout limits its utility for sensor applications. In this paper, we experimentally demonstrate the use of a carbon nanotube (CNT)-hydrogel composite as a biosensor that allows for transduction of the volume change to the change of its electrical conductance upon the binding of target molecules.
A neutravidin (nAv)-responsive conductive hydrogel was developed to demonstrate the detection of target nAv proteins by measuring the electrical conductance of the hydrogel. The high electrical conductivity and high aspect ratio of CNTs make them suitable for forming electrically conductive composite with adjustable functionalities. However, it is extremely difficult to process hydrophobic CNTs in water or hydrophilic hydrogel prepolymer mixtures without forming any aggregated CNT clusters. The issue was mitigated by applying carboxymethyl cellulose (CMC) polymer to serve as a mediator to improve the dispersion of CNT in hydrogel prepolymer solutions. The bioresponsive hydrogel was formed by thermal curing of a prepolymer mixture consisting of two parts – (1) bioresponsive hydrogel frameworks composed of acrylamide (AAm), cross-linker methylene bis-acrylamide (mbisAAm) and succinylated biotin (biotin-NHS), and (2) conductive polymer solution formed by CNT/CMC mixture. To facilitate electrical characterization and sensor device integration, the hybrid composite thin film (< 10 µm) was patterned and cured on interdigitated gold electrodes. Current-voltage measurements under various PBS buffer concentrations and solutions with pH ranging from 2 - 11 suggest that the conductance of the hybrid hydrogel is almost independent of ionic strength and pH level. The former results from the large CNT density in hydrogel whereas the latter pH independency can be attributed to the fact that the pKa’s of AAm (4.7) and CMC (4.5) are very close such that the hydrogel remains ionized throughout the pH range. The conductance of the nAv-repsonisve hydrogel was found to increase with the presence of nAv. Becuse each nAv has four biotin binding sites, the existence of nAv further cross-links the hydrogel framework via binding of up to four biotin moieties resulting in the deswell of hydrogel and therefore decrease the distance between neighboring CNTs. The capability of electrical readout avoids the need of any bulky optics required for conventional optical-based assays.
9:00 PM - BM1.7.05
Understanding the Self-Assembly of Micelles and Micelle Networks Formed by an Array of Amphiphilic Macromolecules Using Dissipative Particle Dynamics
Thomas Deaton 1 , Nan Li 1 , Yaroslava Yingling 1
1 North Carolina State University Raleigh United StatesShow Abstract
Self-assembling polymeric based macromolecules have shown a great deal of promise for many biomedical material applications. While there have been some advancements, many obstacles hinder material development including a shortage in the fundamental understanding of how self-assembly occurs. This establishes the need for developing a method of modelling such interactions on an extremely small scale. Dissipative particle dynamics (DPD) is a coarse-grained meso-scale modeling technique which has proven to be a reliable tool for modeling phase behavior, yet has previously lacked the ability to capture long-range interactions without extremely high computational costs. Such interactions are vital to properly reproducing the assembly of relatively complex polymer chains. Very recently we developed a method to examine single-chain polyelectrolytes by implementing an implicit solvent ionic strength model in combination with a soft repulsive potential. This method was able to appropriately reproduce the morphological impacts on polyelectrolyte assemblies by imparting solvent effects on the self-repulsion of the individual electrolyte monomers. Our work utilizes a similar approach to model two different amphiphilic self-assembling macromolecular systems: diblock ssDNA (ssDNA bonded to a synthetic hydrophobic polymer) and elastin-like polypeptides (ELPs). Both the diblock ssDNA and ELP systems started from randomly distributed conformations throughout a periodic system then assembled into micelles. Upon micelle assembly of the diblock ssDNA, similarly coarse-grained complimentary ssDNA were added, resulting in a bridged network of micelles. From this method, we were able to observe the assembly efficiency as a function of the relationship between length of the ssDNA constituting the micelle to that of the ssDNA complimenting those chains. The ELPs studied were amphiphilic sequence controlled poly-pentapeptides. Four different 120 pentapeptide constructs were studied with varied hydrophilic and hydrophobic segment distributions. The resulting micelles formed by the different constructs were then compared to demonstrate the morphological impacts due to the change in pentapeptide distribution. We were then able to observe specific measurable differences amongst the four different micelle systems such as relative radius of gyration and aggregation. These two modeled systems provide insight into promoting and controlling the assembly of these macromolecules, ultimately building a foundation to which these components can be used to generate impactful biomedical materials.
9:00 PM - BM1.7.06
Nanobody-Conjugated, Quantum Dot-Based Unimolecular Micelles for Targeted Triple Negative Breast Cancer Therapy
Yuyuan Wang 3 1 , Yidan Wang 2 , Guojun Chen 3 1 , Yitong Li 4 , Wei Xu 2 6 , Shaoqin Gong 1 5
3 Department of Materials Science and Engineering University of Wisconsin–Madison Madison United States, 1 Wisconsin Institutes for Discovery University of Wisconsin–Madison Madison United States, 2 McArdle Laboratory for Cancer Research University of Wisconsin–Madison Madison United States, 4 Department of Chemistry Tsinghua University Beijing China, 6 Molecular and Environmental Toxicology Center University of Wisconsin–Madison Madison United States, 5 Department of Biomedical Engineering University of Wisconsin–Madison Madison United StatesShow Abstract
Introduction: Triple negative breast cancer (TNBC) is an aggressive type of breast cancer for which there is no available targeted therapy, thus there is a need to develop novel and effective targeted therapy. Herein, we report a quantum dot (QD)-based multifunctional unimolecular micelles for targeted TNBC therapy. Fluorescent QDs were used as the core of the unimolecular micelle. To achieve active tumor targeting, the unimolecular micelles were conjugated with an anti-epidermal growth factor receptor (EGFR) nanobody (Nb) 7D12. Nb, as a single-domain antibody, has several advantages over whole antibodies and other antibody fragments including smaller sizes (~ 16 kDa) and higher stability. 7D12 Nb can specifically and efficiently bind to the EGFRs overexpressed on the surfaces of the TNBC cells. An anticancer drug, aminoflavone (AF), was loaded into the unimolecular micelles. The cellular uptake of the micelles by TNBC cells were studied in vitro, and the biodistribution and anti-cancer efficacy were studied in vivo.
Methods: The indium phosphide-core, zinc sulfide-shell QDs (InP/ZnS QDs) with fluorescence emission ranging from 500 to 800 nm were first synthesized and their surfaces were then modified with amphiphilic block copolymers poly(lactide)-b-poly(ethylene glycol)-OCH3/maleimide (PLA-PEG-OCH3/Mal). PLA formed a hydrophobic inner region providing a reservoir for AF. 7D12 Nbs were selectively conjugated to the distal ends of PEG by the thiol-maleimide reaction. Fluorescent QDs were used for detecting micelles both in vitro and in vivo. The cellular uptake of the micelles was studied by flow cytometry and fluorescence microscopy. The in vivo biodistribution and anti-cancer efficacy of the AF-loaded micelles were studied in an orthotopic TNBC xenograft mouse model.
Results: Stable QD-based unimolecular micelles were formed in an aqueous solution. 7D12 Nb-conjugated (i.e., targeted) micelles exhibited significantly higher cellular uptake than Nb-lacking (i.e., non-targeted) micelles in EGFR-overexpressing MDA-MB-468 TNBC Cells based on flow cytometry and fluorescence microscopy analyses,indicating excellent targeting capability of the 7D12 Nbs in EGFR-overexpressing TNBC cells. In addition, targeted micelles showed much higher tumor accumulation compared to the non-targeted ones in vivo. More importantly, the AF-loaded