Veerabadran Nalinkanth G, Mongayt Dmitriy, Torchilin Vladimir, Price Ronald R, Lvov Yuri M
Department of Biomedical Engineering, Institute for Micromanufacturing, Louisiana Tech University, Ruston, Louisiana 71272, USA.
Macromol Rapid Commun. 2009 Jan 16;30(2):99-103. doi: 10.1002/marc.200800510. Epub 2008 Oct 30.
The use of tubular halloysite clay as a nanotemplate for layer-by-layer (LbL) shell assembly and its utilization for controlled release of drug macromolecules are studied. The LbL nanoshell allowed additional control for the sustained release of drug loaded halloysite tubes. The number of polymeric layers in the shell and molecular weight of the assembled polymers influences the drug release rate. Three bilayer shells of chitosan and gelatin of 15 nm thicknesses gave the best encapsulation and retardation in the release rate of dexamethasone. An encapsulation of the macromolecules inside the lumen of the biocompatible clay nanotubes coupled with the polyelectrolyte shell formation provides a novel formulation for the controlled release of bioactive agents.
研究了将管状埃洛石粘土用作逐层(LbL)壳组装的纳米模板及其在药物大分子控释中的应用。LbL纳米壳允许对负载药物的埃洛石管的持续释放进行额外控制。壳中聚合物层数和组装聚合物的分子量会影响药物释放速率。三个厚度为15nm的壳聚糖和明胶双层壳在地塞米松释放速率方面表现出最佳的包封和缓释效果。生物相容性粘土纳米管腔内的大分子包封与聚电解质壳的形成相结合,为生物活性剂的控释提供了一种新型制剂。