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混合胶束形成与磷脂酰胆碱:不同分子结构表面活性剂的影响。

Mixed micelle formation with phosphatidylcholines: the influence of surfactants with different molecule structures.

机构信息

Department of Pharmaceutics and Biopharmaceutics, Christian Albrecht University Kiel, Gutenbergstrasse 76, 24118 Kiel, Germany.

出版信息

Int J Pharm. 2010 Mar 15;387(1-2):120-8. doi: 10.1016/j.ijpharm.2009.12.018. Epub 2009 Dec 18.

Abstract

The number of mixed micellar (MM) drug products being introduced into the commercial pharmaceutical market is very limited although there is need for alternative dosage forms for poorly soluble active drug substances. While known systems are composed of phosphatidylcholine and bile salts, it was the aim of this study to investigate if alternative surfactants are able to form isotropically clear solutions over a broad range of concentrations and at higher ratios of phosphatidylcholine (PC). It was a particular challenge of this work to find a MM system with a unimodal particle size distribution since it is known that surfactants often form vesicles with phospholipids instead of MM. The theoretical approach behind this work was the transfer of the packing parameter concept, which describes the molecular association of one amphiphilic species, to the organisation behaviour of two different amphiphilic species (water-insoluble phospholipid+surfactant leading to MM). Therefore the influence of the surfactant molecular geometry on the ability to form MM with phospholipids was investigated. A homologous series of two different surfactant classes, namely polyglycerol esters and sucrose esters, with a large hydrophilic head region leading to a smaller packing parameter were analysed regarding their ability to form clear MM solutions with PC. For comparison, surfactants with no strictly defined partition between a polar head and a non-polar tail (e.g. Poloxamer 188) were tested. Decaglycerol laurate and especially sucrose laurate (SL) were superior compared to all other tested surfactants with respect to their ability to form clear solutions with hydrogenated PC (hPC) at a higher ratio and over a broad range of concentrations while unsaturated PC showed an inferior performance to form MM. The favourite MM system composed of SL with 0.5 weight fractions of hPC formed about 20 nm sized MM in a concentration range of 1.0-80 mg/mL and showing a unimodal particle size distribution with a PDI value <0.1. The results of the study have shown that the transferred packing parameter concept is applicable to the tested surfactants to describe their ability forming mixed micelles with PC.

摘要

尽管对于水溶性差的活性药物物质,需要替代剂型,但目前进入商业制药市场的混合胶束(MM)药物产品的数量非常有限。虽然已知的系统由磷脂酰胆碱和胆汁盐组成,但本研究的目的是研究替代表面活性剂是否能够在较宽的浓度范围内和较高的磷脂酰胆碱(PC)比例下形成各向同性澄清溶液。这项工作的一个特别挑战是找到具有单峰粒径分布的 MM 系统,因为已知表面活性剂通常与磷脂形成囊泡而不是 MM。这项工作背后的理论方法是转移包装参数概念,该概念描述了一种两亲性物质的分子缔合,以研究两种不同的两亲性物质(水溶性差的磷脂+表面活性剂导致 MM)的组织行为。因此,研究了表面活性剂分子几何形状对与磷脂形成 MM 的能力的影响。对具有较大亲水头区域导致较小包装参数的两类不同表面活性剂(聚甘油酯和蔗糖酯)的同系物进行了分析,以研究它们与 PC 形成澄清 MM 溶液的能力。作为比较,还测试了没有严格定义极性头和非极性尾之间分配的表面活性剂(例如泊洛沙姆 188)。与所有其他测试的表面活性剂相比,十甘油月桂酸酯和特别是蔗糖月桂酸酯(SL)在形成高比例和较宽浓度范围内澄清溶液的能力方面具有优势,而不饱和 PC 形成 MM 的性能较差。由 SL 与 0.5 重量分数的氢化 PC(hPC)组成的首选 MM 系统在 1.0-80mg/mL 的浓度范围内形成约 20nm 大小的 MM,并显示出具有 <0.1 的 PDI 值的单峰粒径分布。研究结果表明,转移的包装参数概念可适用于测试的表面活性剂,以描述它们与 PC 形成混合胶束的能力。

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