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In Vivo Activities of Amoxicillin and Amoxicillin-Clavulanate against Streptococcus pneumoniae: Application to Breakpoint Determinations

机译:阿莫西林和阿莫西林克拉维酸盐对肺炎链球菌的体内活性:在断点测定中的应用

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摘要

The in vivo activities of amoxicillin and amoxicillin-clavulanate against 17 strains of Streptococcus pneumoniae with penicillin MICs of 0.12–8.0 mg/liter were assessed in a cyclophosphamide-induced neutropenic murine thigh infection model. Renal impairment was produced by administration of uranyl nitrate to prolong the amoxicillin half-life in the mice from 21 to 65 min, simulating human pharmacokinetics. Two hours after thigh infection with 105 to 106 CFU, groups of mice were treated with 7 mg of amoxicillin per kg of body weight alone or combined with clavulanate (ratio, 4:1) every 8 h for 1 and 4 days. There was an excellent correlation between the MIC of amoxicillin (0.03 to 5.6 mg/liter) and (i) the change in log10 CFU/thigh at 24 h and (ii) survival after 4 days of therapy. Organisms for which MICs were 2 mg/liter or less were killed at 1.4 to 4.2 and 1.6 to 4.1 log10 CFU/thigh at 24 h by amoxicillin and amoxicillin-clavulanate, respectively. The four strains for which MICs were >4 mg/liter grew 0.2 to 2.6 and 0.6 to 2.3 logs at 24 h despite therapy with amoxicillin and amoxicillin-clavulanate, respectively. Infection was uniformly fatal by 72 h in untreated mice. Amoxicillin therapy resulted in no mortality with organisms for which MICs were 1 mg/liter or less, 20 to 40% mortality with organisms for which MICs were 2 mg/liter, and 80 to 100% mortality with organisms for which MICs were 4.0–5.6 mg/liter. Lower and higher doses (0.5, 2, and 20 mg/kg) of amoxicillin were studied against organisms for which MICs were near the breakpoint. These studies demonstrate that a reduction of 1 log10 or greater in CFU/thigh at 24 h is consistently observed when amoxicillin levels exceed the MIC for 25 to 30% of the dosing interval. These studies would support amoxicillin (and amoxicillin-clavulanate) MIC breakpoints of 1 mg/liter for susceptible, 2 mg/liter for intermediate, and 4 mg/liter for resistant strains of S. pneumoniae.
机译:在环磷酰胺诱导的中性粒细胞减少性小鼠大腿感染模型中评估了阿莫西林和阿莫西林-克拉维酸对17株青霉素MIC为0.12-8.0 mg / L的肺炎链球菌菌株的体内活性。模拟人的药代动力学,通过给予硝酸铀酰将小鼠阿莫西林的半衰期从21分钟延长至65分钟,可产生肾脏损害。大腿感染10 5 至10 6 CFU两小时后,每公斤体重单独或与克拉维酸联合使用7 mg阿莫西林治疗小鼠组(比例, 4:1)每8小时1和4天。阿莫西林的MIC(0.03至5.6 mg / L)与(i)24 h log10 CFU /大腿的变化和(ii)治疗4天后的存活率之间存在极好的相关性。 MIC在24小时分别以1.4至4.2和1.6至4.1 log10 CFU /大腿杀死的MICs为2 mg / l或更低的生物被阿莫西林和阿魏西林-克拉维酸盐杀死。尽管使用阿莫西林和阿莫西林-克拉维酸治疗,但MICs> 4 mg / l的四种菌株在24小时仍分别增长了0.2至2.6和0.6至2.3对数。在未经治疗的小鼠中,感染在72 h内均匀致死。阿莫西林治疗对MIC为1 mg / l或更低的微生物没有致死率,对于MIC为2 mg / l的微生物致死率为20%至40%,对于MIC为4.0–5.6的微生物致死率为80%至100%毫克/升。研究了较低和较高剂量(0.5、2和20 mg / kg)的阿莫西林对MIC接近临界点的生物的影响。这些研究表明,当阿莫西林水平在给药间隔的25%至30%内超过MIC时,在24小时内始终观察到CFU /大腿降低1 log10或更大。这些研究将支持阿莫西林(和阿莫西林-克拉维酸)的MIC临界点分别为:易感性肺炎链球菌1 mg / L,中度2 mg / L,抗性肺炎链球菌4 mg / L。

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