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研究胆固醇在基于非离子表面活性剂的双层囊泡形成中的作用:热分析和分子动力学

Investigating the role of cholesterol in the formation of non-ionic surfactant based bilayer vesicles: thermal analysis and molecular dynamics.

作者信息

Wilkhu Jitinder S, Ouyang Defang, Kirchmeier Marc J, Anderson David E, Perrie Yvonne

机构信息

School of Life and Health Sciences, Aston University, Birmingham B4 7ET, UK.

Variation Biotechnologies, 222 Third Street, Suite 2241, Cambridge, MA 02142, USA.

出版信息

Int J Pharm. 2014 Jan 30;461(1-2):331-41. doi: 10.1016/j.ijpharm.2013.11.063. Epub 2013 Dec 11.

Abstract

The aim of this research was to investigate the molecular interactions occurring in the formulation of non-ionic surfactant based vesicles composed monopalmitoyl glycerol (MPG), cholesterol (Chol) and dicetyl phosphate (DCP). In the formulation of these vesicles, the thermodynamic attributes and surfactant interactions based on molecular dynamics, Langmuir monolayer studies, differential scanning calorimetry (DSC), hot stage microscopy and thermogravimetric analysis (TGA) were investigated. Initially the melting points of the components individually, and combined at a 5:4:1 MPG:Chol:DCP weight ratio, were investigated; the results show that lower (90 °C) than previously reported (120-140 °C) temperatures could be adopted to produce molten surfactants for the production of niosomes. This was advantageous for surfactant stability; whilst TGA studies show that the individual components were stable to above 200 °C, the 5:4:1 MPG:Chol:DCP mixture show ∼2% surfactant degradation at 140 °C, compared to 0.01% was measured at 90 °C. Niosomes formed at this lower temperature offered comparable characteristics to vesicles prepared using higher temperatures commonly reported in literature. In the formation of niosome vesicles, cholesterol also played a key role. Langmuir monolayer studies demonstrated that intercalation of cholesterol in the monolayer did not occur in the MPG:Chol:DCP (5:4:1 weight ratio) mixture. This suggests cholesterol may support bilayer assembly, with molecular simulation studies also demonstrating that vesicles cannot be built without the addition of cholesterol, with higher concentrations of cholesterol (5:4:1 vs 5:2:1, MPG:Chol:DCP) decreasing the time required for niosome assembly.

摘要

本研究的目的是调查在由单棕榈酸甘油酯(MPG)、胆固醇(Chol)和磷酸二鲸蜡酯(DCP)组成的非离子表面活性剂基囊泡制剂中发生的分子相互作用。在这些囊泡的制剂中,基于分子动力学、Langmuir单分子层研究、差示扫描量热法(DSC)、热台显微镜和热重分析(TGA)研究了热力学属性和表面活性剂相互作用。最初,分别研究了各组分的熔点,以及以5:4:1的MPG:Chol:DCP重量比混合后的熔点;结果表明,可采用比先前报道的温度(120 - 140°C)更低(90°C)的温度来制备用于生产非离子表面活性剂囊泡的熔融表面活性剂。这对表面活性剂稳定性有利;虽然TGA研究表明各组分在200°C以上是稳定的,但5:4:1的MPG:Chol:DCP混合物在140°C时表面活性剂降解约2%,而在90°C时测得的降解率为0.01%。在这个较低温度下形成的非离子表面活性剂囊泡具有与文献中通常报道的使用较高温度制备的囊泡相当的特性。在非离子表面活性剂囊泡的形成过程中,胆固醇也起着关键作用。Langmuir单分子层研究表明,在MPG:Chol:DCP(5:4:1重量比)混合物中,胆固醇不会插入单分子层。这表明胆固醇可能支持双层组装,分子模拟研究也表明,不添加胆固醇就无法构建囊泡,较高浓度的胆固醇(5:4:1对比5:2:1,MPG:Chol:DCP)会减少非离子表面活性剂囊泡组装所需的时间。

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