quantitative modeling of the high-throughput production and in vivo kinetics of (drug-encapsulating) liposomes定量建模的大规模生产和体内动力学(drug-encapsulating)脂质体.pdfVIP

Quantitative Modeling of the High-Throughput Production and In Vivo Kinetics of (Drug-Encapsulating) Liposomes Albert Wong* Program in Biological and Biomedical Sciences, Yale University, New Haven, Connecticut, United States of America Abstract In developing liposomes for in vivo use, it is important to design the liposomes to have optimal in vivo kinetics, and it is also necessary to identify optimal high-throughput production conditions for these liposomes. Previous work has not definitively established the general relationship between liposomes’ configuration and composition, and their in vivo kinetics. Also, no straightforward method exists to calculate optimal liposome high-throughput production conditions for specific liposome compositions. This work presents first-principles quantitative correlations describing liposomes’ in vivo drug leakage and vascular mass transfer kinetics. This work further presents a simple quantitative model relating specific liposome compositions to ideal high-throughput production parameters. The results have implications for the identification of promising liposome compositions via high-throughput screening methodologies, as well as the design and optimization of high-throughput reactors for liposome production. Citation: Wong A (2010) Quantitative Modeling of the High-Throughput Production and In Vivo Kinetics of (Drug-Encapsulating) Liposomes. PLoS ONE 5(4): e10280. doi:10.1371/journal.pone.0010280 Editor: Christophe Egles, Tufts University, United States of America Received December 8, 2009; Accepted March 29, 2010; Published April 23, 2010 Copyright: 2010 Albert Wong. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original