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环丙沙星在健康墨西哥志愿者中的药代动力学。

Pharmacokinetics of ciprofloxacin in healthy Mexican volunteers.

作者信息

Escobar Yesenia, Hoyo-Vadillo Carlos

机构信息

Colegio en Ciencia Farmacéutica A.C., Mexico City, Mexico.

出版信息

Arzneimittelforschung. 2003;53(9):664-7. doi: 10.1055/s-0031-1299809.

Abstract

Ciprofloxacin (CAS 85721-33-1) is a gyrase inhibitor used against a wide number of bacteria which develops a very low bacterial resistance. Its pharmacokinetics has been extensively studied using two main methods, liquid chromatography and microbiological assay. The pharmacokinetics of ciprofloxacin administered orally was evaluated in healthy Mexican volunteers after a dose of 500 mg. Ciprofloxacin was assayed from plasma by a specific HPLC method reading absorbance at 280 nm. Pharmacokinetic parameters were similar to reported values, including a previous study on Mexican healthy volunteers with the microbiological assay. AUC was 12.11 mg h/l, Cmax 2.44 mg/l, tmax 0.79 h and half-life 3.8 h. tmax was slightly shorter than those in other studies. Ciprofloxacin presented no adverse reactions and can be dosed to people with Amerindian origin in the same dose regimes as prescribed to Caucasians in order to achieve minimal inhibitory concentrations against a wide range of microbial pathogens.

摘要

环丙沙星(CAS 85721-33-1)是一种拓扑异构酶抑制剂,可用于对抗多种细菌,且产生的细菌耐药性极低。其药代动力学已通过两种主要方法,即液相色谱法和微生物测定法进行了广泛研究。在500毫克剂量后,对健康的墨西哥志愿者口服环丙沙星的药代动力学进行了评估。通过在280纳米处读取吸光度的特定高效液相色谱法从血浆中测定环丙沙星。药代动力学参数与报告值相似,包括之前一项针对墨西哥健康志愿者的微生物测定研究。曲线下面积(AUC)为12.11毫克·小时/升,最大血药浓度(Cmax)为2.44毫克/升,达峰时间(tmax)为0.79小时,半衰期为3.8小时。达峰时间略短于其他研究中的时间。环丙沙星未出现不良反应,并且可以按照开给白种人的相同剂量方案给予美洲印第安人后裔,以达到对多种微生物病原体的最低抑菌浓度。

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