Microfluidic Synthesis of Nano-Liposomal Anesthetics

Published

May 12, 2013

Author(s)

Wyatt N. Vreeland, Renee R. Hood, Eric Kendall, Mariana Junqueira, Julia Finkel, Don L. DeVoe

Abstract

Topical anesthesia has the ability to provide painless application of pain management medications for minor procedures such as venipuncture, particularly in the pediatric population. Liposomes have been proposed as a highly advantageous nanocarrier for dermal transport of drugs. Unlike conventional liposome preparation methods, which yield polydisperse populations of liposomes which are too large to passively transverse dermal layers (typically >80 nm), the recently developed microfluidic method for liposome synthesis provides an approach for producing nearly-monodisperse vesicles of tunable size which can achieve a range of size not achievable by traditional methods (approximately 40 nm and below). In this study, we have utilized a previously-demonstrated microfluidic method for continuous-flow synthesis of small, nearly-monodisperse liposomes and demonstrated size-dependent passive uptake into porcine dermal tissue.

Proceedings Title

TechConnect World, Summit and Innovation Showcase 2013

Conference Dates

May 12-16, 2013

Conference Location

National Harbor, MD

Pub Type

Conferences

Keywords

nanoparticle, liposome, microfluidics, drug delivery

Citation

Vreeland, W. , Hood, R. , Kendall, E. , Junqueira, M. , Finkel, J. and DeVoe, D. (2013), Microfluidic Synthesis of Nano-Liposomal Anesthetics, TechConnect World, Summit and Innovation Showcase 2013, National Harbor, MD (Accessed February 5, 2025)