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13种β-内酰胺类抗生素在人粪便中的非酶失活作用

The non-enzymatic inactivation of thirteen beta-lactam antibiotics in human faeces.

作者信息

Jansen G, Weissing F, de Vries-Hospers H, Tonk R, van der Waaij D

机构信息

Laboratory of Medical Microbiology, University of Groningen, The Netherlands.

出版信息

Infection. 1992 Nov-Dec;20(6):355-9. doi: 10.1007/BF01710684.

Abstract

In order to obtain a method that could predict the in vitro inactivation of an antibiotic in the digestive tract, the non-enzymatic inactivation of 13 beta-lactam antibiotics by human faeces was investigated. Benzylpenicillin, amoxicillin, amoxicillin/clavulanate, cloxacillin, piperacillin, temocillin, cefuroxime, cefamandole, cephradine, cefotaxime, ceftazidime, aztreonam and imipenem were mixed in six graded concentrations with faecal suspensions of 30 healthy volunteers. After incubation the remaining antimicrobial activity was measured by means of a serial dilution method. A relationship between the initial antibiotic concentration (Aia) and the remaining antimicrobial activity after incubation (Asd) was derived, namely: Asd = 1/2[(Aia-K-F)+square root ((Aia-K-F)2 + 4 K Aia)]. The parameters K and F represent the intrinsic dissociation constant and the amount of available bindingsites in the faeces, respectively. Asd values were predicted with a reasonable degree of accuracy for all thirteen antibiotics. Dissociation constants differed significantly between the penicillins and the cephalosporins but F- values did not differ between cephalosporins and penicillins.

摘要

为了获得一种能够预测抗生素在消化道中体外失活的方法,研究了人粪便对13种β-内酰胺类抗生素的非酶促失活作用。将苄青霉素、阿莫西林、阿莫西林/克拉维酸、氯唑西林、哌拉西林、替莫西林、头孢呋辛、头孢孟多、头孢拉定、头孢噻肟、头孢他啶、氨曲南和亚胺培南与30名健康志愿者的粪便悬液按六种梯度浓度混合。孵育后,通过系列稀释法测定剩余的抗菌活性。得出初始抗生素浓度(Aia)与孵育后剩余抗菌活性(Asd)之间的关系,即:Asd = 1/2[(Aia - K - F) + √((Aia - K - F)² + 4K Aia)]。参数K和F分别代表粪便中的固有解离常数和可用结合位点的数量。对所有13种抗生素的Asd值都能以合理的准确度进行预测。青霉素类和头孢菌素类的解离常数有显著差异,但头孢菌素类和青霉素类的F值没有差异。

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