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组织水平对于预测抗生素疗效和确定剂量的意义。

Significance of tissue levels for prediction of antibiotic efficacy and determination of dosage.

作者信息

Carbon C

机构信息

Médecine Interne, Hôpital Bichat-Claude Bernard, Paris, France.

出版信息

Eur J Clin Microbiol Infect Dis. 1990 Jul;9(7):510-6. doi: 10.1007/BF01964293.

Abstract

Determination of tissue levels is widely thought to provide useful information in the investigation of a new antibiotic, however this assumption is not fully justified. In this paper the following questions are covered. Firstly, the methodological problems encountered in the measurement of antibiotic levels in solid tissues and extravascular fluids are described. Secondly, the difficulties encountered in interpreting tissue concentrations are discussed, given the heterogeneity of distribution of drugs, potential intracellular penetration, binding to tissue proteins and local factors reducing antibacterial activity. Thirdly, the respective importance of animal and human data on tissue levels for prediction of efficacy is analysed. In some animal models it is possible to study the conditions affecting antibacterial activity and to obtain data relevant to the clinical situation. However, the inoculum effect, the metabolism of bacteria, the mechanism of the bactericidal action of drugs and the type of infected tissue are important factors to be taken into account. In humans, data obtained from infected tissue is sparse and contributes little to knowledge. Knowledge of tissue levels may be important for establishing whether data obtained in animals can be applied to humans or not. Fourthly, the importance of tissue levels in determining antibiotic dosages is evaluated. In humans, tissue levels are of limited value in the determination of unitary dose and dosage intervals in relation to the clinical response. Trough serum levels of free drug, half-life at the beta-phase and rate of in vitro killing are the most important parameters to be considered. Their relative importance depends mainly on the mode of action of the drug.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

人们普遍认为,测定组织药物浓度有助于新型抗生素的研究,但这一假设并不完全合理。本文探讨了以下问题:首先,阐述了在测定实体组织和血管外液中抗生素浓度时遇到的方法学问题;其次,鉴于药物分布的异质性、潜在的细胞内渗透、与组织蛋白的结合以及降低抗菌活性的局部因素,讨论了解释组织浓度时遇到的困难;第三,分析了动物和人体组织药物浓度数据对疗效预测的各自重要性。在一些动物模型中,可以研究影响抗菌活性的条件并获得与临床情况相关的数据。然而,接种菌量效应、细菌代谢、药物杀菌作用机制和感染组织类型都是需要考虑的重要因素。在人体中,从感染组织获得的数据稀少,对知识贡献不大。了解组织药物浓度对于确定动物数据是否可应用于人类可能很重要;第四,评估了组织药物浓度在确定抗生素剂量方面的重要性。在人体中,就临床反应而言,组织药物浓度在确定单一剂量和给药间隔方面价值有限。游离药物的血清谷浓度、β相半衰期和体外杀菌速率是需要考虑的最重要参数。它们的相对重要性主要取决于药物的作用方式。(摘要截选至250词)

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