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表面活性剂对β-内酰胺类抗生素水稳定性和溶解度的影响。

Effects of surfactants on the aqueous stability and solubility of beta-lactam antibiotics.

作者信息

Tsuji A, Miyamoto E, Matsuda M, Nishimura K, Yamana T

出版信息

J Pharm Sci. 1982 Dec;71(12):1313-8. doi: 10.1002/jps.2600711203.

Abstract

Studies were undertaken to elucidate the interaction between beta-lactam antibiotics and surfactant micelles and to examine the effects of surfactants on their aqueous stability and solubility. The apparent binding constant of the micelle-antibiotic complex was determined as a function of the solution pH at 37 degrees and mu = 0.15 by the dynamic dialysis method and hydrolysis study. In the interaction with nonionic and anionic micelles of polyoxyethylene-23-lauryl ether (I) and sodium lauryl sulfate (II), large differences were noted in the binding constants between the undissociated and ionized species of penicillins. However, the cationic surfactants, cetyltrimethylammonium bromide (III), showed no significant difference in the binding constants for both species. Acid degradation of penicillins was protected in micellar solutions of I and III but was facilitated in micelles of II. The surfactants exerted no influence on the neutral degradation of the antibiotics used. The solubilization of penicillin V acid by micelles of I was studied at pH 2.0 and 35 degrees. The solubility increased threefold in the presence of 10 mM I.

摘要

开展了多项研究以阐明β-内酰胺抗生素与表面活性剂胶束之间的相互作用,并研究表面活性剂对其水稳定性和溶解度的影响。通过动态透析法和水解研究,在37℃和μ = 0.15条件下,测定了胶束 - 抗生素复合物的表观结合常数与溶液pH值的函数关系。在与聚氧乙烯 - 23 - 月桂醚(I)和十二烷基硫酸钠(II)的非离子和阴离子胶束相互作用时,观察到青霉素未解离和离子化形式之间的结合常数存在很大差异。然而,阳离子表面活性剂十六烷基三甲基溴化铵(III)对这两种形式的结合常数没有显著差异。在I和III的胶束溶液中,青霉素的酸降解受到保护,但在II的胶束中则加速。表面活性剂对所用抗生素的中性降解没有影响。在pH 2.0和35℃条件下研究了I的胶束对青霉素V酸的增溶作用。在存在10 mM I的情况下,溶解度增加了三倍。

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