Application of TPGS in polymeric nanoparticulate drug delivery system

被引:63
作者
Mu, L
Seow, PH
机构
[1] Natl Univ Singapore, Div Bioengn, Singapore 117576, Singapore
[2] Nanyang Technol Univ, Singapore MIT Alliance, Singapore 639798, Singapore
[3] Natl Univ Singapore, Dept Chem Engn, Singapore 119260, Singapore
关键词
biodegradable polymer; surfactant; stabiliser; emulsifier; controlled release; nanoparticles; D-alpha-tocopheryl polyethylene glycol 1000 succinate; paclitaxel; taxol; drug-cell membrane interaction;
D O I
10.1016/j.colsurfb.2005.08.016
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
D-alpha-Tocopheryl polyethylene glycol 1000 succinate (TPGS) has great potential in pharmacology and nanotechnology. The present work investigated the molecular behaviour of TPGS at the air-water interface, its effect on a model bio-membrane composed of dipalmitoylphosphatidyl choline (DPPC) lipid monolayer, and the interaction between the TPGS coated nanoparticles with the lipid model membrane. Paclitaxel loaded polymeric nanoparticles with TPGS as surfactant stabiliser were fabricated and characterised in terms of their drug incorporation capability and release kinetics. The result showed that TPGS exhibited notable effect on the surface properties of air-water interface as well as the lipid monolayer. The inter-particle force and the interaction between nanoparticles and lipid monolayer varied with the surface substance. The penetration of various nanoparticles into the model membrane indicated that an optimal balance between hydrophilicity and hydrophobicity on nanoparticle surface is needed to achieve an effective cellular uptake of nanoparticles. The results also demonstrate that the drug incorporation capability and the release characteristics of drug-loaded nanoparticles can be influenced by surfactant stabiliser. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:90 / 97
页数:8
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