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两性霉素 B 从可生物降解的聚(乳酸-共-乙醇酸)纳米粒中的载药和释放。

Loading and release of amphotericin-B from biodegradable poly(lactic-co-glycolic acid) nanoparticles.

机构信息

Pharmaceutics Division, Central Drug Research Institute (CSIR), M. G. Marg, Lucknow 226001, India.

出版信息

J Biomed Nanotechnol. 2011 Feb;7(1):118-20. doi: 10.1166/jbn.2011.1230.

Abstract

Amphotericin B (AmB)-loaded poly(lactic-co-glycolic acid, PLGA) nanoparticles (NP) were prepared by solvent displacement. NP of size 160.7 +/- 10.45 nm, with a polydispersity index of 0.093 +/- 0.012 and a zeta-potential of -15.5 +/- 7.2 mV had satisfactory drug entrapment efficiency (42.5 +/- 6.41%). Biphasic drug release characterized by an initial burst followed by subsequent sustained release was observed. Applicability against visceral leishmaniasis and cancer is under investigation.

摘要

两性霉素 B(AmB)负载的聚乳酸-共-羟基乙酸(PLGA)纳米粒(NP)通过溶剂置换法制备。所得 NP 的粒径为 160.7 ± 10.45nm,多分散指数为 0.093 ± 0.012,ζ 电位为-15.5 ± 7.2mV,具有令人满意的药物包封效率(42.5 ± 6.41%)。观察到具有初始突释随后持续释放特征的两相药物释放。其对内脏利什曼病和癌症的适用性正在研究中。

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