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Degradation kinetics and mechanism of aminocephalosporins in aqueous solution: Cefadroxil

โœ Scribed by Akira Tsuji; Emi Nakashima; Yoshiharu Deguchi; Kazunori Nishide; Takayoshi Shimizu; Sumio Horiuchi; Kiyoyasu Ishikawa; Tsukinaka Yamana


Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
909 KB
Volume
70
Category
Article
ISSN
0022-3549

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โœฆ Synopsis


as well as nonpolar systems. An effort is being made to obtain W without solubility data, with the possibility of finding a physicochemical basis for W and/or a group contribution method for estimating this solventsolute interaction term.

It is interesting to observe in Table 111 and in Figs. 1 and 5 that small (fractional to 1 or 2%) differences between 6162, the geometric mean, and W, the correct adhesive energy density, may cause large differences (25-75%) between ideal and real solubilities. It will challenge the investigator to measure and calculate energies within 5-50 cal/mole required for an independent measure of W for accurate estimation of solubilities. The prediction of solubility using W from group contributions would represent a step toward a better understanding of the behavior of drug molecules in polar and nonpolar solvent systems.

REFERENCES


๐Ÿ“œ SIMILAR VOLUMES


Kinetics and mechanism of degradation of
โœ S. M. Berge; N. L. Henderson; M. J. Frank ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 481 KB ๐Ÿ‘ 2 views

The degradation kinetics and mechanism of a potent new cephalosporin, cefotaxime sodium, in aqueous solution were investigated at pH 0-10 at 25 degrees and an ionic strength of 0.5. The degradation rates were determined by high-pressure liquid chromatography and were observed to follow pseudo first-