๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Study of the solubilization of gliclazide by aqueous micellar solutions

โœ Scribed by Khouloud A. Alkhamis; Hussien Allaboun; Wafa'a Y. Al-Momani


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
126 KB
Volume
92
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.

โœฆ Synopsis


It was of interest to increase the solubility of gliclazide in aqueous media. Therefore, solubilization of gliclazide in a variety of surfactants was investigated. Anionic and cationic surfactants exhibited dramatic solubilizing ability for gliclazide, whereas nonionic surfactants showed significantly lower solubilizing ability. It was found that gliclazide solubility increases with increasing the carbon chain length of cationic surfactants and decreases with increasing the carbon chain length of anionic surfactants. The solubilization data were analyzed on the basis of a pseudo-phase model with gliclazide exhibiting moderate partition coefficients into the micellar phase. The possible sites of solubilization of gliclazide in the micelle were examined by studying the effect of NaCl on solubilization and by comparing the absorption spectra of gliclazide in different solvents. The results obtained from these two experiments indicated that gliclazide is solubilized mainly in the inner core of the cationic surfactant micelles and in the outer regions of the anionic surfactant micelles.


๐Ÿ“œ SIMILAR VOLUMES


Determining thermodynamic quantities of
โœ Alicia G. Peterson; Joe P. Foley ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 843 KB

Using the van't Hoff relationship, the enthalpy and entropy of transfer from the aqueous to a chiral micellar phase was measured for 12 pairs of enantiomeric pharmaceutical compounds, including p-agonists, p-blockers, and other p-amino alcohols. Selectivities, distribution coefficients, and Gibbs fr

Solubilization of salicylamide and aceta
โœ Sunil P. Shah; Douglas R. Flanagan ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 459 KB

The effect of self-association of the antihistaminic drugs pheniramine, chlorpheniramine, and brompheniramine as their maleate salts on the solubilization of salicylamide and acetaminophen in aqueous solution has been investigated. The total solubility of salicylamide increased nonlinearly at lower