Degradation kinetics and mechanism of aminocephalosporins in aqueous solution: Cefadroxil
โ 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
No coin nor oath required. For personal study only.
โฆ 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
๐ SIMILAR VOLUMES
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-