Variable-temperature Raman spectro-microscopy for a comprehensive analysis of the conformational order in PEGylated lipids

被引:21
作者
Bista, Rajan K. [1 ]
Bruch, Reinhard F. [1 ,2 ]
Covington, Aaron M. [1 ,3 ]
机构
[1] Univ Nevada, Dept Phys, Reno, NV 89557 USA
[2] Univ Nevada, Elect & Biomed Engn Dept, Reno, NV 89557 USA
[3] Nevado Terawatt Facil, Reno, NV 89506 USA
关键词
conformational order; phase transitions; QuSomes; self-forming lipids; PHASE-TRANSITIONS; INFRARED-SPECTROSCOPY; BEHAVIOR; PHOSPHATIDYLCHOLINE; CHOLESTEROL; DISPERSIONS; LECITHIN; CHAINS; ACID; LONG;
D O I
10.1002/jrs.2156
中图分类号
O433 [光谱学];
学科分类号
070207 [光学];
摘要
The investigation of phase transitions and associated changes in the conformational order of lipids is of importance in various research areas dealing with phenomena such as the formation and fusion of vesicles, transmembrane diffusion and membrane interactions with drugs and proteins. In this article, we have focused on the study of thermotropic phase behaviors and associated changes in the conformational order of two newly developed synthetic PEGylated lipids trademarked as QuSomes. In contrast to conventional phospholipids, this new kind of lipid forms liposomes spontaneously upon hydration, without the supply of external activation energy. Variable-temperature Raman spectro-microscopy has been employed in order to plot the transition temperature profiles showing the phase behavior of these new lipids composed of 1,2-dimyristoyl-rac-glycerol-3-dodecaethylene glycol (GDM-12) and 1,2-distearoyl-rac-glycerol-3-triicosaethylene glycol (GDS-23). Furthermore, several spectral indicators were calculated and correlated which allowed for the deduction of various aspects of molecular structure as well as intramolecular motion and intermolecular interactions. To confirm the observations, differential scanning calorimetry (DSC) was applied and revealed a good agreement with the Raman spectroscopy results. Finally, this information may find application in various studies including the development of lipid-based novel substances and drug delivery systems. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:463 / 471
页数:9
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