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大环内酯类抗生素的药代动力学及向组织间液的转运:红霉素、克拉霉素和阿奇霉素的比较

Pharmacokinetics of Macrolide Antibiotics and Transport into the Interstitial Fluid: Comparison among Erythromycin, Clarithromycin, and Azithromycin.

作者信息

Kobuchi Shinji, Kabata Teruhiko, Maeda Koki, Ito Yukako, Sakaeda Toshiyuki

机构信息

Department of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.

出版信息

Antibiotics (Basel). 2020 Apr 22;9(4):199. doi: 10.3390/antibiotics9040199.

Abstract

Recent research has found higher levels and longer total exposure of azithromycin, a macrolide antibiotic agent, in the interstitial fluid of the skin than in the plasma. This unique distribution is expected to contribute to its antimicrobial activity at the primary infection site. However, it remains unclear whether this characteristic distribution in the extracellular tissue space is common to macrolide antibiotics or if it is azithromycin-specific, with most macrolides largely localized intracellularly. In this study, we investigated pharmacokinetic characteristics of erythromycin and clarithromycin in the interstitial fluid of the skin of rats after intravenous drug administration, and compared the results with our previously reported results on azithromycin. Interstitial fluid samples were directly collected from a pore on the skin using a dissolving microneedle array. We found that the total macrolide concentrations in the interstitial fluid were significantly different among three macrolides. The rank order of the interstitial fluid-plasma concentration ratio was azithromycin (3.8 to 4.9) > clarithromycin (1.2 to 1.5) > erythromycin (0.27 to 0.39), and this ratio was stable after dosing, whereas higher drug levels in the skin tissue than in the plasma were observed for all three macrolides. Our results suggest that lower erythromycin concentrations in the interstitial fluid than in the plasma contributes to the emergence of bacterial resistance in the extracellular tissue space. Monitoring of total macrolide concentrations in interstitial fluid may provide valuable information regarding antimicrobial effects and the emergence of bacterial resistance for the development of an appropriate pharmacokinetics-pharmacodynamics-based dosing strategy.

摘要

近期研究发现,大环内酯类抗生素阿奇霉素在皮肤组织液中的浓度水平更高,且总暴露时间更长,高于其在血浆中的水平。这种独特的分布情况有望增强其在主要感染部位的抗菌活性。然而,目前尚不清楚细胞外组织空间中的这种特征性分布是大环内酯类抗生素所共有的,还是阿奇霉素所特有的,因为大多数大环内酯类药物主要定位于细胞内。在本研究中,我们调查了静脉给药后大鼠皮肤组织液中红霉素和克拉霉素的药代动力学特征,并将结果与我们之前报道的阿奇霉素的结果进行了比较。使用溶解微针阵列直接从皮肤上的一个小孔采集组织液样本。我们发现,三种大环内酯类药物在组织液中的总浓度存在显著差异。组织液与血浆浓度比的排序为阿奇霉素(3.8至4.9)>克拉霉素(1.2至1.5)>红霉素(0.27至0.39),给药后该比值保持稳定,而所有三种大环内酯类药物在皮肤组织中的水平均高于血浆。我们的结果表明,组织液中红霉素浓度低于血浆浓度,这导致细胞外组织空间中细菌耐药性的出现。监测组织液中大环内酯类药物的总浓度,可能为制定基于药代动力学-药效学的合适给药策略,提供有关抗菌效果和细菌耐药性出现的有价值信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5e3/7235806/7867a453a081/antibiotics-09-00199-g001.jpg

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