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喹诺酮与阳离子的相互作用:综述

Quinolone-cation interactions: a review.

作者信息

Lomaestro B M, Bailie G R

机构信息

Pharmacy Department, Albany Medical Center, NY 12208.

出版信息

DICP. 1991 Nov;25(11):1249-58. doi: 10.1177/106002809102501115.

Abstract

The quinolone class of antibiotics is enjoying a recent resurgence in interest and use due to the development of improved compounds. Norfloxacin, ciprofloxacin, and, most recently, ofloxacin have been marketed. Enoxacin and other agents are in various stages of investigation. These newer compounds are often used for indications not successfully treated by the original quinolones, or in some cases, not optimally treated with any previously available oral antibiotic. A potential problem with the increasing use of quinolone-type antibiotics for systemic illness is the chelation and inactivation of these compounds by several cations. One outcome of these potential interactions is a possible reduction in bioavailability and effectiveness of quinolone compounds. A review of the literature on quinolone-cation interactions, in vivo and in vitro significance, and recommendations to avoid potential problems are provided.

摘要

由于改进型化合物的研发,喹诺酮类抗生素近来在关注度和使用方面再度兴起。诺氟沙星、环丙沙星以及最近的氧氟沙星已投放市场。依诺沙星和其他药物正处于不同的研究阶段。这些新型化合物常用于治疗原喹诺酮类药物未能成功治愈的病症,或者在某些情况下,用于治疗任何先前可用口服抗生素都无法达到最佳效果的病症。喹诺酮类抗生素用于全身性疾病的使用日益增加,一个潜在问题是这些化合物会被几种阳离子螯合并失活。这些潜在相互作用的一个后果可能是喹诺酮类化合物的生物利用度和有效性降低。本文提供了关于喹诺酮 - 阳离子相互作用、体内和体外意义的文献综述,以及避免潜在问题的建议。

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