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|Author(s):||Wyatt N. Vreeland; Renee R. Hood; Eric Kendall; Mariana Junqueira; Julia Finkel; Don L. DeVoe;|
|Title:||Microfluidic Synthesis of Nano-Liposomal Anesthetics|
|Published:||May 12, 2013|
|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:||TechConnect World, Summit and Innovation Showcase 2013|
|Location:||National Harbor, MD|
|Dates:||May 12-16, 2013|
|Keywords:||nanoparticle, liposome, microfluidics, drug delivery|