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用于静脉给药的表面(电荷)修饰亚微米乳剂对血浆蛋白的体外吸附

In vitro adsorption of plasma proteins onto the surface (charges) modified-submicron emulsions for intravenous administration.

作者信息

Tamilvanan Shunmugaperumal, Schmidt Sven, Müller Rainer H, Benita Simon

机构信息

Department of Pharmaceutics, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel.

出版信息

Eur J Pharm Biopharm. 2005 Jan;59(1):1-7. doi: 10.1016/j.ejpb.2004.07.001.

Abstract

Surface (charge) modified submicron emulsions (cationic and anionic) were prepared following the well established combined emulsification techniques and characterized for their droplet size distribution and surface charge. The effect of these emulsions on in vitro adsorption of plasma proteins was investigated by means of two dimensional polyacrylamide gel electrophoresis (2D PAGE). The presence of poloxamer 188 in tested emulsions effectively eliminated the adsorption of the larger proteins like immunoglobulins, fibrinogen, etc. However, depending on the type of surface charges, the smaller proteins such as apolipoproteins and albumin were almost completely adsorbed onto the submicron emulsions. Indeed, when compared to marketed lipofundin MCT 10%-and deoxycholic acid-based anionic emulsions, the adsorption of apolipoprotein, especially apoA-1, was approximately three times more on stearylamine-and oleylamine-based cationic emulsions and oleic acid-based anionic emulsions. In addition, the ratio between the apoA-1 and apoA-IV was found to be 1 for lipofundin MCT 10% whereas it was about 0.26 for deoxycholic acid-based anionic emulsion and above 5 for oleic acid-based anionic emulsions and cationic emulsions. This indicates that emulsions having similar surface/interfacial charge imparted by different anion-forming stabilizers (oleic or deoxycholic acids) exhibited markedly different protein adsorption patterns.

摘要

采用成熟的复合乳化技术制备了表面(电荷)改性的亚微米乳液(阳离子型和阴离子型),并对其粒径分布和表面电荷进行了表征。通过二维聚丙烯酰胺凝胶电泳(2D PAGE)研究了这些乳液对血浆蛋白体外吸附的影响。测试乳液中泊洛沙姆188的存在有效地消除了免疫球蛋白、纤维蛋白原等较大蛋白质的吸附。然而,根据表面电荷的类型,载脂蛋白和白蛋白等较小的蛋白质几乎完全吸附在亚微米乳液上。事实上,与市售的10%中链甘油三酯脂肪乳和基于脱氧胆酸的阴离子乳液相比,基于硬脂胺和油胺的阳离子乳液以及基于油酸的阴离子乳液对载脂蛋白,尤其是载脂蛋白A-1的吸附大约多三倍。此外,发现10%中链甘油三酯脂肪乳中载脂蛋白A-1与载脂蛋白A-IV的比例为1,而基于脱氧胆酸的阴离子乳液约为0.26,基于油酸的阴离子乳液和阳离子乳液则高于5。这表明由不同的阴离子形成稳定剂(油酸或脱氧胆酸)赋予相似表面/界面电荷的乳液表现出明显不同的蛋白质吸附模式。

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