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[氟喹诺酮类药物对金黄色葡萄球菌的突变预防浓度]

[Mutant prevention concentrations of fluoroquinolones for Staphylococcus aureus].

作者信息

Cui Jun-chang, Liu You-ning, Wang Rui, Liang Bei-bei, Pei Fei, Zheng Zhuan-jie

机构信息

Department of Respiratory Diseases, Chinese People's Liberation Army General Hospital, Beijing 100853, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2004 Nov 17;84(22):1863-6.

Abstract

OBJECTIVE

To establish a method to measure mutant prevention concentration (MPC) in vitro, and to measure MPC of fluoroquinolones for staphylococcus aureus.

METHODS

The staphylococcus aureus strain ATCC25923 and 20 ciprofloxacin-susceptible clinical isolates were enriched in broth, and the bacterial concentrations were adjusted to 10(10) colony forming units per milliliter. The minimal inhibitory concentration (MIC), MIC for 99% of input cells (MIC99), provisional MPC (MPCpr) and MPC of moxifloxacin, gatifloxacin, pasufloxacin and ciprofloxacin for staphylococcus aureus were determined by agar plates dilution method.

RESULTS

The MPC of moxifloxacin, gatifloxacin, pasufloxacin and ciprofloxacin for staphylococcus aureus strain ATCC25923 were 0.18, 0.3, 0.75 and 1.8 microg/ml, and the MPC/MIC99 were 9.0, 7.5, 8.0 and 10.6 respectively. The MPC for 90% of the isolates (MPCpr90) of moxifloxacin, gatifloxacin, pasufloxacin and ciprofloxacin for 20 staphylococcus aureus clinical isolates were 1, 1, 4 and 8 microg/ml, and the MPCpr90/MIC90 were 8, 8, 16 and 16 respectively.

CONCLUSION

The capacity of moxifloxacin and gatifloxacin for restricting the selection of staphylococcus aureus resistant mutants were stronger than that of pasufloxacin and ciprofloxacin. Combined with pharmacokinetic parameters, moxifloxacin and gatifloxacin may restrict the selective enrichment of resistant mutants among ciprofloxacin-susceptible staphylococcus aureus clinical isolates, and ciprofloxacin is expected to selectively enrich mutants easily.

摘要

目的

建立体外测定突变预防浓度(MPC)的方法,并测定氟喹诺酮类药物对金黄色葡萄球菌的MPC。

方法

将金黄色葡萄球菌ATCC25923菌株及20株对环丙沙星敏感的临床分离株在肉汤中富集,调整细菌浓度至每毫升10(10)菌落形成单位。采用琼脂平板稀释法测定莫西沙星、加替沙星、帕苏沙星和环丙沙星对金黄色葡萄球菌的最低抑菌浓度(MIC)、99%接种菌的MIC(MIC99)、暂定MPC(MPCpr)和MPC。

结果

莫西沙星、加替沙星、帕苏沙星和环丙沙星对金黄色葡萄球菌ATCC25923菌株的MPC分别为0.18、0.3、0.75和1.8μg/ml,MPC/MIC99分别为9.0、7.5、8.0和10.6。莫西沙星、加替沙星、帕苏沙星和环丙沙星对20株金黄色葡萄球菌临床分离株的90%分离株的MPC(MPCpr90)分别为1、1、4和8μg/ml,MPCpr90/MIC90分别为8、8、16和16。

结论

莫西沙星和加替沙星限制金黄色葡萄球菌耐药突变体选择的能力强于帕苏沙星和环丙沙星。结合药代动力学参数,莫西沙星和加替沙星可能限制环丙沙星敏感的金黄色葡萄球菌临床分离株中耐药突变体的选择性富集,而环丙沙星有望容易地选择性富集突变体。

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