体外动态模型中耐利奈唑胺金黄色葡萄球菌浓度依赖性富集。

Q4 Medicine Antibiotiki i Khimioterapiya Pub Date : 2016-01-01
K N Alieva, E N Strukova, M V Golikova, Yu A Portnoy, A A Firsov
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引用次数: 0

摘要

为了建立耐药金黄色葡萄球菌突变体富集与利奈唑胺浓度-时间曲线下的日面积(AUC24)与MIC的关系,采用体外动态模型,将3株金黄色葡萄球菌的利奈唑胺敏感和耐药细胞混合接种于利奈唑胺,每日2次。模拟药代动力学曲线模拟了使用利奈唑胺剂量超过32倍AUC24/MIC比值的5天治疗。在治疗开始后的120小时内,每天对暴露于利奈唑胺的葡萄球菌进行种群分析。在最低和最高的AUC24/MIC比值处,观察到对抗生素的2X、4X和8XMIC耐药的突变体富集较少(如果有的话),而在中间AUC24/MIC处,观察到耐药突变体富集。与暴露后突变体数量(NM)相比,AUBCm(抗性突变体时间过程下的面积)是建立AUC24/MIC与抗性关系的更合适的端点。
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Concentration-Dependent Enrichment of Linezolid-Resistant Staphylococcus aureus in an in vitro Dynamic Model.

To establish the relationships between the enrichment of resistant Staphylococcus aureus mutants and the ratio of daily area under the concentration - time curve (AUC24) to the MIC of linezolid, a mixed inoculum of linezolid-susceptible and -resistant cells of three strains of S.aureus was exposed to twice daily linezolid in an in vitro dynamic model. Simulated pharmacokinetic profiles mimicked five-day treatments with linezolid dosing over a 32-fold range of the AUC24/MIC ratio. Population analysis of linezolid-exposed staphylococci was performed daily over 120 h after the start of the treatments. Minor if any enrichment of mutants resistant to 2X, 4X and 8XMIC of antibiotic was observed at the lowest and the highest AUC24/MIC ratios in contrast to pro- nounced enrichment of resistant mutants at the intermediate AUC24/MICs. An integral parameter AUBCm, the area under the time course of resistance mutants, was shown to be a more appropriate endpoint to establish AUC24/MIC relationships with resistance than postexposure number of mutants (NM).

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来源期刊
Antibiotiki i Khimioterapiya
Antibiotiki i Khimioterapiya Medicine-Infectious Diseases
CiteScore
0.80
自引率
0.00%
发文量
46
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