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采用纳米沉淀技术制备高载药量的草药亲水性药物聚合物纳米粒:一种质量源于设计的方法

Development of polymeric nanoparticles with highly entrapped herbal hydrophilic drug using nanoprecipitation technique: an approach of quality by design.

作者信息

Vuddanda Parameswara Rao, Mishra Amit, Singh Sanjay Kumar, Singh Sanjay

机构信息

Department of Pharmaceutics, Indian Institute of Technology (Banaras Hindu University) , Varanasi, Uttar Pradesh , India.

出版信息

Pharm Dev Technol. 2015;20(5):579-87. doi: 10.3109/10837450.2014.908302. Epub 2014 May 15.

Abstract

The intention of this study is to achieve higher entrapment efficiency (EE) of berberine chloride (selected hydrophilic drug) using nanoprecipitation technique. The solubility of drug was studied in various pH buffers (1.2-7.2) for selection of aqueous phase and stabilizer. Quality by design (QbD)-based 3(2) factorial design were employed for optimization of formulation variables; drug to polymer ratio (X1) and surfactant concentration (X2) on entrapment efficiency (EE), particle size (PS) and polydispersity index (PDI) of the nanoparticles. The nanoparticles were subjected to solid state analysis, in vitro drug release and stability study. The aqueous phase and stabilizer selected for the formulations were pH 4.5 phthalate buffer and surfactant F-68, respectively. The formulation (F-6) containing drug to polymer ratio (1:3) and stabilizer (F-68) concentration of 50 mM exhibited best EE (82.12%), PS (196.71 nm), PDI (0.153). The various solid state characterizations assured that entrapped drug is amorphous and nanoparticles are fairly spherical in shape. In vitro drug release of the F-6 exhibited sustained release with non-Fickian diffusion and stable at storage condition. This work illustrates that the proper selection of aqueous phase and optimization of formulation variables could be helpful in improving the EE of hydrophilic drugs by nanoprecipitation technique.

摘要

本研究旨在利用纳米沉淀技术提高盐酸小檗碱(所选亲水性药物)的包封率(EE)。研究了药物在各种pH缓冲液(1.2 - 7.2)中的溶解度,以选择水相和稳定剂。采用基于质量源于设计(QbD)的3(2)析因设计来优化配方变量;药物与聚合物比例(X1)和表面活性剂浓度(X2)对纳米颗粒的包封率(EE)、粒径(PS)和多分散指数(PDI)的影响。对纳米颗粒进行了固态分析、体外药物释放和稳定性研究。为配方选择的水相和稳定剂分别是pH 4.5的邻苯二甲酸盐缓冲液和表面活性剂F - 68。含有药物与聚合物比例为(1:3)和稳定剂(F-68)浓度为50 mM的配方(F-6)表现出最佳的包封率(82.12%)、粒径(196.71 nm)和多分散指数(0.153)。各种固态表征确保了包封的药物为无定形,且纳米颗粒形状相当球形。F-6的体外药物释放呈现出非菲克扩散的缓释特性,并且在储存条件下稳定。这项工作表明,水相的适当选择和配方变量的优化有助于通过纳米沉淀技术提高亲水性药物的包封率。

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