Lamcharfi E, Cohen-Solal C, Parquet M, Lutton C, Dupré J, Meyer C
Département de Chimie, Université Sidi Mohammed ben Abdellah, Faculté des Sciences et Techniques Fès-Saiss, Fès, Maroc.
Eur Biophys J. 1997;25(4):285-91. doi: 10.1007/s002490050040.
The aim of this study was to analyse the Raman and infrared spectra of eight common mammalian bile acids in order to identify intermolecular interactions between hydroxyl and carbonyl groups. The results are considered in the light of the new hydrophilic/hydrophobic classification of bile acids. The alcohol OH group of the hydrophobic bile acids forms different intermolecular bonds. The most hydrophobic bile acid, lithocholic acid forms polymers, and this may explain its very low water solubility. The hydrophilic bile acids have some of their alcohol OH groups free of any intermolecular interaction. The strongly hydrophilic murideoxycholic acid also forms dimers, again consistent with a very low water solubility. The proposed structural arrangements are in agreement with published crystallographic studies.
本研究的目的是分析八种常见哺乳动物胆汁酸的拉曼光谱和红外光谱,以确定羟基和羰基之间的分子间相互作用。根据胆汁酸新的亲水/疏水分类来考虑结果。疏水性胆汁酸的醇羟基形成不同的分子间键。疏水性最强的胆汁酸石胆酸形成聚合物,这可能解释了其极低的水溶性。亲水性胆汁酸的一些醇羟基没有任何分子间相互作用。强亲水性的鼠李脱氧胆酸也形成二聚体,这同样与其极低的水溶性一致。所提出的结构排列与已发表的晶体学研究结果一致。