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An in vitro study on the compatibility and precipitation of a combination of ciprofloxacin and vancomycin in human vitreous

机译:环丙沙星和万古霉素在人玻璃体内的相容性和沉淀的体外研究

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摘要

>Aims: To investigate the precipitation process of a mixture of vancomycin and ciprofloxacin by equilibrium dialysis and its subsequent effect on the level of available free antibiotics.>Methods: Concentrations of vancomycin and ciprofloxacin in an equilibrium dialysis chamber were measured during the equilibrium process by high performance liquid chromatography and fluorescence polarisation immunoassay. Normal saline (NS), balanced salt solution plus (BSS Plus), and vitreous were used separately as the medium of dialysis.>Results: Precipitation of ciprofloxacin occurred on incubation at 37°C. It formed precipitate on its own or when mixed with vancomycin in all the three media of NS, BSS Plus, and vitreous. There was more precipitation at higher initial ciprofloxacin concentrations; at 25.0 mg/l about 75% free drug in BSS Plus was lost after 72 hours. The extent of precipitation was similar in both NS and BSS Plus. In the dialysis chambers, 20 mg/l ciprofloxacin dialysed against 125 mg/l vancomycin was reduced to a concentration about 5.0 mg/l after 168 hours. Precipitation of vancomycin was negligible. Ciprofloxacin precipitated in vitreous at body temperature, irrespective of the presence of vancomycin. Even after precipitation, the resultant concentration of ciprofloxacin was still higher than the MIC90 of the drug against most Gram negative organisms.>Conclusions: Based on this in vitro study, ciprofloxacin precipitated in vitreous at body temperature, irrespective of the presence of vancomycin or the medium for intravitreal injection. The resultant amount of ciprofloxacin was still higher than the MIC90 of the drug against most Gram negative organisms after precipitation. The authors suggest ciprofloxacin in place of ceftazidime when used in combination with vancomycin for treatment of infective endophthalmitis.
机译:>目的:研究平衡透析对万古霉素和环丙沙星混合物的沉淀过程及其对可用游离抗生素水平的影响。>方法:万古霉素和环丙沙星的浓度在平衡过程中,通过高效液相色谱和荧光偏振免疫分析法测量平衡透析室中的血浆。分别使用生理盐水(NS),平衡盐溶液加(BSS Plus)和玻璃体作为透析介质。>结果:37°C孵育时出现环丙沙星沉淀。它独自或与万古霉素在NS,BSS Plus和玻璃体的所有三种介质中形成沉淀。环丙沙星初始浓度较高时会有更多的沉淀。 72小时后,以25.0 mg / l的浓度,BSS Plus中约有75%的游离药物流失。 NS和BSS Plus的沉淀程度相似。在透析室中,在168小时后,将针对125 mg / l万古霉素透析的20 mg / l环丙沙星的浓度降低至约5.0 mg / l。万古霉素的沉淀可忽略不计。不管是否存在万古霉素,环丙沙星在体温下都会在玻璃体内沉淀。即使沉淀后,环丙沙星的最终浓度仍高于大多数革兰氏阴性菌对药物的MIC90。>结论:根据这项体外研究,环丙沙星在体温下在玻璃体中沉淀,无论万古霉素或玻璃体内注射介质的存在。沉淀后,对于大多数革兰氏阴性生物体,环丙沙星的最终含量仍高于药物的MIC90。作者建议环丙沙星与万古霉素联用代替头孢他啶治疗感染性眼内炎。

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