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血清蛋白结合会抑制抗生素的组织渗透吗?

Does serum protein binding inhibit tissue penetration of antibiotics?

作者信息

Bergan T, Engeset A, Olszewski W

机构信息

Department of Microbiology, University of Oslo, Norway.

出版信息

Rev Infect Dis. 1987 Jul-Aug;9(4):713-8. doi: 10.1093/clinids/9.4.713.

Abstract

Accumulated data on the penetration of 15 antibacterial agents into peripheral human lymph are reviewed. The major factor determining extravascular penetration is the level of serum protein binding. The penetration ratios of extravascular and serum levels diminish gradually as the level of protein binding increases. However, even at the highest protein-binding levels, distinct lymph concentrations are observed. The degree of penetration ranges from 100% for the antibiotic with the lowest level of serum protein binding (gentamicin, no drug bound) to 20% for that with the highest level of protein binding (flucloxacillin, 96% bound).

摘要

本文综述了15种抗菌药物渗透进入人体外周淋巴液的累积数据。决定血管外渗透的主要因素是血清蛋白结合水平。随着蛋白结合水平的升高,血管外与血清水平的渗透比逐渐降低。然而,即使在最高的蛋白结合水平下,仍可观察到明显的淋巴液浓度。渗透程度范围从血清蛋白结合水平最低的抗生素(庆大霉素,无药物结合)的100%到蛋白结合水平最高的抗生素(氟氯西林,96%结合)的20%。

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