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载药纳米结构脂质载体的制备及表征。

Preparation and characterization of nanostructured lipid carriers loaded traditional Chinese medicine, zedoary turmeric oil.

机构信息

School of Pharmacy, Department of Pharmaceutics, Shenyang Pharmaceutical University, Shenyang, Liaoning, PR China.

出版信息

Drug Dev Ind Pharm. 2010 Jul;36(7):773-80. doi: 10.3109/03639040903485716.


DOI:10.3109/03639040903485716
PMID:20136496
Abstract

BACKGROUND: The objective of this work was to study the preparation and characteristics of zedoary turmeric oil (ZTO), a traditional Chinese oily medicine, loaded with nanostructured lipid carriers (NLCs). METHOD: Aqueous dispersions of NLC were successfully prepared by melt-emulsification technique using Crodamol SS as the solid lipid, Miglyol 812N as the liquid oil, and soybean phosphatidylcholine (SbPC) as the emulsifier. Properties of NLC such as the particle size and its distribution, the transmission electron microscope (TEM), drug entrapment efficiency (EE), and drug release behavior were investigated, respectively. The Germacrone blood concentration after intravenous administration of ZTO-NLC was determined and compared with that of ZTO-injection. RESULT: As a result, the drug EEs were improved by adding the liquid lipid into the solid lipid of nanoparticles (SLNs). In vitro drug release experiments indicated that the prepared NLC could enhance the drug release rate over the SLN, and the drug release rate could be adjusted by the liquid lipid content in lipid nanospheres. X-ray and differential scanning calorimetry (DSC) measurements revealed that imperfect crystallization occurred in the inner core of the NLC particles. CONCLUSION: The results suggest that the presented NLC system might be a promising intravenous dosage form of water-insoluble oily drugs.

摘要

背景:本研究旨在制备莪术油纳米结构脂质载体(NLC)并对其进行研究。莪术油是一种传统的中药油剂。

方法:采用熔融乳化技术,以 Crodamol SS 为固体脂质,Miglyol 812N 为液体油,大豆卵磷脂(SbPC)为乳化剂,成功制备了 NLC 的水相分散体。分别考察了 NLC 的粒径及其分布、透射电镜(TEM)、载药量(EE)和药物释放行为等性质。考察了莪术油 NLC 静脉给药后的倍半蒈烯血药浓度,并与莪术油注射液进行了比较。

结果:结果表明,在纳米粒的固体脂质中加入液体脂质可以提高药物 EE。体外药物释放实验表明,所制备的 NLC 可以提高药物的释放速率,并且可以通过脂质纳米球中的液体脂质含量来调节药物释放速率。X 射线和差示扫描量热法(DSC)测量表明,NLC 颗粒的内核中发生了不完全结晶。

结论:结果表明,所提出的 NLC 系统可能是一种有前途的水不溶性油类药物的静脉给药剂型。

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