The formation of reversed micellar systems composed of phosphatidylcholine (PC) and fatty acid was newly demonstrated by a significant increase in water content in the organic ethyl oleate phase when the micelles were prepared by the contact method. The solubilized water concentration in the reverse
The Ionization Behavior of Fatty Acids and Bile Acids in Micelles and Membranes
β Scribed by Donald M. Small; Donna J. Cabral; David P. Cistola; John S. Parks; James A. Hamilton
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 320 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0270-9139
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β¦ Synopsis
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 linear function of the state of ionization of the carboxyl group. Thus, by measuring the chemical shift as a function of the amount of acid or base added to a solution, the state of ionization and the apparent pKa of the carboxyl group may be determined. The method is illustrated in this paper using butyric acid, and results (given as apparent pKa values) are tabulated for a variety of fatty acids and cholic acid in different environments such as monomeric solutions, micelles, membranes
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