Nesthus I, Haneberg B, Glette J, Solberg C O
Acta Pathol Microbiol Immunol Scand B. 1985 Jun;93(3):189-94. doi: 10.1111/j.1699-0463.1985.tb02875.x.
Macrophages obtained by culturing human blood monocytes were incubated with Staphylococcus aureus for phagocytosis to occur and exposed to gentamicin, rifampin, clindamycin or trimethoprim/sulphamethoxazole. The macrophage-associated bacteria were protected against gentamicin at low concentrations (1 mg/l) and trimethoprim/sulphamethoxazole. However, high concentrations of gentamicin and clindamycin reduced the number of bacteria, indicating that these drugs penetrated into human macrophages and killed phagocytosed bacteria. Rifampin, even at low concentrations (0.5 mg/l), caused a marked reduction in macrophage-associated bacteria, implying that the drug penetrated into the phagocytes and retained its effect in the cells most effectively.
将通过培养人血单核细胞获得的巨噬细胞与金黄色葡萄球菌一起孵育,使其发生吞噬作用,然后将其暴露于庆大霉素、利福平、克林霉素或甲氧苄啶/磺胺甲恶唑中。巨噬细胞相关的细菌在低浓度(1毫克/升)的庆大霉素和甲氧苄啶/磺胺甲恶唑作用下受到保护。然而,高浓度的庆大霉素和克林霉素减少了细菌数量,表明这些药物可穿透进入人巨噬细胞并杀死被吞噬的细菌。即使在低浓度(0.5毫克/升)下,利福平也能显著减少巨噬细胞相关细菌的数量,这意味着该药物能有效穿透进入吞噬细胞并在细胞内保持其作用。