April 7 - 11, 2025
Seattle, Washington
Symposium Supporters
2025 MRS Spring Meeting & Exhibit
SB05.04.05

Mucopenetrating Janus Nanoparticles (JNPs) Targeting Oral Squamous Cell Carcinoma

When and Where

Apr 8, 2025
5:00pm - 7:00pm
Summit, Level 2, Flex Hall C

Presenter(s)

Co-Author(s)

Yifei He1,Albert Chang2,Joerg Lahann2,Susan Mallery3

University of Michigan-Ann Arbor1,University of Michigan–Ann Arbor2,The Ohio State University3

Abstract

Yifei He1,Albert Chang2,Joerg Lahann2,Susan Mallery3

University of Michigan-Ann Arbor1,University of Michigan–Ann Arbor2,The Ohio State University3
Oral squamous cell carcinoma (OSCC) is an aggressive cancer associated with high morbidity and mortality. Preemptive interventions and localized drug delivery systems have shown potential in enhancing treatment outcomes; however, the development of broadly applicable and efficient local delivery systems remains a significant barrier. In response to these challenges, bi-compartmental (Janus) nanoparticles (JNPs) present a novel therapeutic solution by improving targeted drug delivery, reducing side effects, and enabling sustained release. JNPs possess a unique dual-compartment structure, allowing for the simultaneous delivery of two distinct therapeutic agents. Additionally, they can be engineered to include imaging agents for real-time monitoring of drug distribution and efficacy.
In this study, we report the development of a mucopenetrating JNPs system, designed for dual-drug loading and sustained release in OSCC treatment. JNPs are fabricated through Electrohydrodynamic (EHD) co-jetting, which utilizes laminar flow of two parallel streams through capillary needles without convective mixing. EHD co-jetting efficiently creates JNPs by preserving the initial arrangement of input polymers during solvent evaporation. Characterization of the JNPs including Scanning Electron Microscopy (SEM) revealed an average diameter of approximately 400 nm. Drug release studies conducted via High-Performance Liquid Chromatography (HPLC) and customized ELISA demonstrated controlled, sustained release of retinoid and antibody drugs. These findings underscore the potential of JNPs to enhance targeted drug delivery and improve therapeutic outcomes in OSCC patients.

Keywords

protein

Symposium Organizers

Dale Huber, Sandia National Laboratories
Yongfeng Zhao, Jackson State University
Linh Nguyen, University College London
Daishun Ling, Shanghai Jiao Tong University
Nguyen Thanh, Univ College London

Symposium Support

Silver
Jackson State University

Session Chairs

Dale Huber
Daishun Ling
Linh Nguyen
Yongfeng Zhao

In this Session