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超临界抗溶剂沉淀法制备葛根素、磷脂及其复合物微粒的过程参数与形态

Process parameters and morphology in puerarin, phospholipids and their complex microparticles generation by supercritical antisolvent precipitation.

作者信息

Li Ying, Yang Da-Jian, Chen Shi-Lin, Chen Si-Bao, Chan Albert Sun-Chi

机构信息

Shanghai Jiao Tong University, Shanghai, China.

出版信息

Int J Pharm. 2008 Jul 9;359(1-2):35-45. doi: 10.1016/j.ijpharm.2008.03.022. Epub 2008 Mar 25.

Abstract

The aim of the study was to develop and evaluate a new method for the production of puerarin phospholipids complex (PPC) microparticles. The advanced particle formation method, solution enhanced dispersion by supercritical fluids (SEDS), was used for the preparation of puerarin (Pur), phospholipids (PC) and their complex particles for the first time. Evaluation of the processing variables on PPC particle characteristics was also conducted. The processing variables included temperature, pressure, solution concentration, the flow rate of supercritical carbon dioxide (SC-CO2) and the relative flow rate of drug solution to CO2. The morphology, particle size and size distribution of the particles were determined. Meanwhile Pur and phospholipids were separately prepared by gas antisolvent precipitation (GAS) method and solid characterization of particles by the two supercritical methods was also compared. Pur formed by GAS was more orderly, purer crystal, whereas amorphous Pur particles between 0.5 and 1microm were formed by SEDS. The complex was successfully obtained by SEDS exhibiting amorphous, partially agglomerated spheres comprised of particles sized only about 1microm. SEDS method may be useful for the processing of other pharmaceutical preparations besides phospholipids complex particles. Furthermore adopting a GAS process to recrystallize pharmaceuticals will provide a highly versatile methodology to generate new polymorphs of drugs in addition to conventional techniques.

摘要

本研究的目的是开发并评估一种制备葛根素磷脂复合物(PPC)微粒的新方法。首次采用先进的颗粒形成方法——超临界流体增强溶液分散法(SEDS)来制备葛根素(Pur)、磷脂(PC)及其复合颗粒。同时还研究了工艺变量对PPC颗粒特性的影响。工艺变量包括温度、压力、溶液浓度、超临界二氧化碳(SC-CO2)的流速以及药物溶液与CO2的相对流速。测定了颗粒的形态、粒径和粒径分布。同时,分别采用气体抗溶剂沉淀法(GAS)制备了Pur和磷脂,并比较了两种超临界方法制备颗粒的固体特性。GAS法制备的Pur更规整、晶体更纯,而SEDS法制备的是粒径在0.5至1微米之间的无定形Pur颗粒。通过SEDS成功获得了复合物,其呈现出无定形、部分团聚的球体,由粒径仅约1微米的颗粒组成。SEDS法可能不仅适用于磷脂复合颗粒,还可用于其他药物制剂的制备。此外,除了传统技术外,采用GAS工艺对药物进行重结晶将提供一种高度通用的方法来生成药物的新晶型。

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