๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Bile Acids and Bile Salts: Ionization and Solubility Properties

โœ Scribed by Martin C. Carey


Publisher
John Wiley and Sons
Year
1984
Tongue
English
Weight
612 KB
Volume
4
Category
Article
ISSN
0270-9139

No coin nor oath required. For personal study only.

โœฆ Synopsis


The number, position and orientation of nuclear OH substituents profoundly influence the equilibrium solubilities of undissociated bile acids in water. Estimates from several studies range from 5 x lo-' for lithocholic acid to 1.6 x


๐Ÿ“œ SIMILAR VOLUMES


Bilirubin Chemistry, Ionization and Solu
โœ J. Donald OSTROW; Lillian Celic ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 1010 KB

Bilirubin is a linear tetrapyrrole whose conformation is affected by internal hydrogen bonds formed between the carboxyl side chains and dipyrromethenone rings. Structural variations include: constitutional isomerism of the vinyl or carboxyethyl side chains, geometric isomerism of the methene bridge

Bile Salt Structure and Phase Equilibria
โœ Martin C. Carey ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 577 KB

The hydrophilic-hydrophobic balance of bile salt monomers can be readily quantified by their elution sequence during reverse-phase high-performance liquid chromatography. Such studies have demonstrated that subtle variations in bile salt structure have profound effects on the hydrophilic-hydrophobic

Bile salts and gallstone disease
โœ Colin MacKay ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 799 KB
Wetting properties of bile salt solution
โœ Paul E. Luner ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 271 KB

The objective of this study was to determine the extent to which specific bile salt solutions and compendial dissolution media differ in their ability to wet a model surface. Solutions were examined in the concentration range of bile salts found in the gastrointestinal tract and at pH values approxi

The Ionization Behavior of Fatty Acids a
โœ Donald M. Small; Donna J. Cabral; David P. Cistola; John S. Parks; James A. Hami ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 320 KB

The ionization behavior of carboxylic acids including aliphatic chain fatty acids and bile acids in solutions, micelles, membranes and proteins is of considerable biological interest. The 13C nuclear magnetic resonance chemical shift of carboxyl carbon of a variety of acids has been shown to be a li