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沉降场流分离后肠外脂肪乳剂中的成分异质性。

Compositional heterogeneity in parenteral lipid emulsions after sedimentation field flow fractionation.

作者信息

Venkatesh S, Li J, Caldwell K D, Anderson B D

机构信息

Department of Pharmaceutics & Pharmaceutical Chemistry, University of Utah, Salt Lake City, Utah 84112, USA.

出版信息

J Pharm Sci. 1998 Jul;87(7):859-66. doi: 10.1021/js970399y.

DOI:10.1021/js970399y
PMID:9649355
Abstract

This study examines the size and compositional heterogeneity of particles in a commercial lipid emulsion (Intralipid) before and after equilibration with penclomedine, a highly lipophilic cytotoxic agent. Emulsions were fractionated by sedimentation field-flow fractionation (sedFFF), and particle sizes of the monodisperse fractions were determined by photon correlation spectroscopy. The triglyceride (TG), phosphatidylcholine (PC), and penclomedine (in drug loaded emulsions) contents in each fraction were determined by HPLC. The aqueous-entrapped volume within Intralipid was determined to be approximately 10% by size-exclusion chromatography using [3H]mannitol. Thirteen sedFFF fractions collected from the drug free emulsions yielded particles ranging in size from 154 to 423 nm. Total channel recoveries were 89% and 95% for TG and PC, respectively. Apparent particle densities varied significantly with size, suggesting heterogeneity in composition as confirmed by PC/TG mass ratios which varied dramatically. Computer fits of the distribution profiles suggested populations of phospholipid vesicles and oil droplets containing excess phospholipid in addition to classical emulsion droplets. Drug loading induced a significant shift of the predominant triglyceride containing population to a larger particle size. The penclomedine distribution profile closely mimicked that of the TG rather than the PC fraction. These studies suggest the need to consider not only size distribution but also compositional distribution in characterizing parenteral emulsions.

摘要

本研究考察了一种市售脂质乳剂(英脱利匹特)在与高度亲脂性细胞毒性药物喷司他丁平衡前后颗粒的大小及组成异质性。通过沉降场流分级法(sedFFF)对乳剂进行分级,并采用光子相关光谱法测定单分散级分的颗粒大小。采用高效液相色谱法(HPLC)测定各分级中甘油三酯(TG)、磷脂酰胆碱(PC)以及(载药乳剂中的)喷司他丁的含量。使用[³H]甘露醇通过尺寸排阻色谱法测定英脱利匹特中截留的水相体积约为10%。从不含药物的乳剂中收集的13个sedFFF分级产生了大小范围为154至423nm的颗粒。TG和PC的总柱回收率分别为89%和95%。表观颗粒密度随颗粒大小显著变化,这表明组成存在异质性,PC/TG质量比的显著变化证实了这一点。分布曲线的计算机拟合表明,除了经典的乳剂液滴外,还存在磷脂囊泡群以及含有过量磷脂的油滴。载药导致主要含甘油三酯群体向更大颗粒大小的显著转变。喷司他丁的分布曲线与TG的分布曲线密切相似,而非PC级分的分布曲线。这些研究表明,在表征肠胃外乳剂时,不仅需要考虑大小分布,还需要考虑组成分布。

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