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自上而下和自下而上的方法在低溶解度药物紫杉醇水纳米胶体的生产中的应用。

Top-down and bottom-up approaches in production of aqueous nanocolloids of low solubility drug paclitaxel.

机构信息

Institute for Micromanufacturing, Chemistry Department, Louisiana Tech University, Ruston, LA 71272, USA.

出版信息

Phys Chem Chem Phys. 2011 May 21;13(19):9014-9. doi: 10.1039/c0cp02549f. Epub 2011 Mar 25.

Abstract

Nano-encapsulation of a poorly soluble anticancer drug was demonstrated with a sonication assisted layer-by-layer polyelectrolyte coating (SLbL). We changed the strategy of LbL-encapsulation from making microcapsules with many layers in the walls for encasing highly soluble materials to using a very thin polycation/polyanion coating on low solubility nanoparticles to provide them with good colloidal stability. SLbL encapsulation of paclitaxel resulted in stable 100-200 nm diameter colloids with a high electrical surface ξ-potential (of -45 mV) and drug content in the nanoparticles of 90 wt%. In the top-down approach, nanocolloids were prepared by rupturing a powder of paclitaxel using ultrasonication and simultaneous sequential adsorption of oppositely charged biocompatible polyelectrolytes. In the bottom-up approach paclitaxel was dissolved in organic solvent (ethanol or acetone), and drug nucleation was initiated by the addition of aqueous polyelectrolyte assisted by ultrasonication. Paclitaxel release rates from such nanocapsules were controlled by assembling multilayer shells with variable thicknesses and were in the range of 10-20 h.

摘要

采用超声辅助层层聚电解质包衣(SLbL)对难溶性抗癌药物进行纳米封装。我们改变了 LbL 封装的策略,从用壁上的许多层制作微胶囊来封装高可溶性物质,改为在低溶解度纳米颗粒上使用非常薄的聚阳离子/聚阴离子涂层,为其提供良好的胶体稳定性。紫杉醇的 SLbL 包封导致稳定的 100-200nm 直径胶体,具有高的电表面 ξ-电势(-45mV)和纳米颗粒中 90wt%的药物含量。在自上而下的方法中,通过超声破碎紫杉醇粉末并同时顺序吸附带相反电荷的生物相容性聚电解质来制备纳米胶体。在自下而上的方法中,紫杉醇溶解在有机溶剂(乙醇或丙酮)中,并通过超声辅助添加带相反电荷的水相聚电解质引发药物成核。通过组装具有可变厚度的多层壳来控制此类纳米胶囊的药物释放率,释放时间在 10-20 小时范围内。

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