Solubility and Dissolution Thermodynamic Data of Cefpiramide in Pure Solvents and Binary Solvents

被引:0
作者
Fengxiang Tang
Shan Wu
Suying Zhao
机构
[1] Fuzhou University,College of Chemistry
[2] Fuzhou University,College of Chemical Engineering
来源
Journal of Solution Chemistry | 2017年 / 46卷
关键词
Cefpiramide; Solubility; Pure solvent; Binary solvent mixture; Dissolution thermodynamics;
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摘要
The solubility of cefpiramide in five pure solvents (water, ethanol, 1-propanol, 2-propanol, and 1-butanol) and two binary solvent systems (water + ethanol or water + 2-propanol) was measured by a steady-state method, from 278.2 to 303.2 K, under atmospheric pressure. The initial mole fraction of alcohol (ethanol or 2-propanol) in the binary systems ranged from 0 to 1. It is found that the solubility increases with increasing temperature in the experimental range and shows a quasi-S-shaped curve with the increase of the initial mole fraction of alcohol. The modified Apelblat equation was used to simulate the solubility data, and gives a maximum mean relative deviation (MRD) of 0.47% for the single solvent systems, and a maximum MRD of 1.03 and 1.15% for the ethanol + water and 2-propanol + water systems, respectively. The combined model of the Jouyban–Acree and modified Apelblat equations, both temperature-dependent and solvent-composition-dependent, was simplified to correlate the solubility data of binary solvent mixtures in the initial mole fraction range of alcohol from 0 to 0.9, and gives a MRD of 9.83 and 6.49% for the ethanol +water and 2-propanol + water systems, respectively. The dissolution thermodynamic properties in the pure solvents and two binary mixtures were calculated based on the van’t Hoff equation. The calculation results indicate that the dissolution process of cefpiramide is endothermic in the pure solvents, and entropically driven in the four alcohols but not in water. The dissolution process is endothermic in the two binary mixtures.
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页码:1556 / 1574
页数:18
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共 81 条
[1]  
Kato M(1982)Antibacterial activities of SM-1652 compared with those of other broad-spectrum cephalosporins Antimicrob. Agents Chemother. 22 721-727
[2]  
Inoue M(1985)Comparative in vitro activities of cefpiramide and apalcillin individually and in combination Antimicrob. Agents Chemother. 27 782-790
[3]  
Mitsuhashi M(1985)Cefpiramide: comparative in vitro activity and & β-lactamase stability J. Antimicrob. Chemother. 16 315-325
[4]  
Alan JD(1983)In vitro antibacterial activity of SM-1652, a new broad-spectrum cephalosporin with anti-pseudomonal activity Antimicrob. Agents Chemother. 23 195-200
[5]  
Eliopoulos GM(1984)In vitro antibacterial activity of cefpiramide Antimicrob. Agents Chemother. 25 368-372
[6]  
Ferraro MJ(1984)Comparative in vitro activities of cefpiramide and apalcillin against anaerobic bacteria Antimicrob. Agents Chemother. 25 162-164
[7]  
Moellering RC(2012)Thermostability comparison of two solid states of cefpiramide J. Anal. Bioanal. 3 142-148
[8]  
Barry AL(2013)Dissociation constant and solubility of ( J. Chem. Eng. Data 58 1265-1270
[9]  
Jones RN(1952))-2-hydroxy-4-phenylbutyric acid J. Am. Chem. Soc. 74 4138-4140
[10]  
Thornsberry C(2015)Enhanced solubility in solvent mixtures. I. The system phenanthrene–cyclohexane–methylene iodide J. Mol. Liq. 203 98-103