DCDR Spectroscopy as Efficient Tool for Liposome Studies: Aspect of Preparation Procedure Parameters

E. Kočišová, A. Vodáková, M. Procházka
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引用次数: 7

Abstract

Drop-coating deposition Raman (DCDR) spectroscopy was employed to study liposome suspensions. The method is based on a specific drying process on the hydrophobic surface that efficiently accumulates the macromolecular sample in a ring of the edge of the dried drop. We studied liposome suspensions purchased from two sources (Avanti Polar Lipids, Inc. and Sigma-Aldrich, Co.) and prepared under different conditions. Structure of the dried drop substantially depends on the lipid concentration, lipid composition of the sample, and used solvent. Optimal lipid concentration is about 0.3 mg/ml in all cases, asolectin and DSPC suspensions form compact dried drops when dissolved in water and phosphate buffer, respectively. Drying process of the sample drop does not influence the initial phase state (gel or liquid-crystalline) of the studied liposomes excepting DSPC from Sigma-Aldrich, Co.
ddr光谱学作为脂质体研究的有效工具:制备工艺参数方面
采用滴涂沉积拉曼(DCDR)光谱研究脂质体悬浮液。该方法基于疏水表面上的特定干燥过程,该过程有效地将大分子样品积聚在干燥液滴边缘的环中。我们研究了从两个来源(Avanti Polar Lipids, Inc.和Sigma-Aldrich, Co.)购买的脂质体悬浮液,并在不同条件下制备。干燥液滴的结构基本上取决于样品的脂质浓度、脂质组成和所用溶剂。在所有情况下,最佳脂质浓度约为0.3 mg/ml,凝集素和dsc悬浮液分别溶于水和磷酸盐缓冲液时形成致密的干燥滴状。除Sigma-Aldrich公司的dsc外,样品滴的干燥过程不影响所研究脂质体的初始相态(凝胶或液晶)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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