首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Comparison of high-pressure liquid chromatography and bioassay for determination of ciprofloxacin in serum and urine.
【2h】

Comparison of high-pressure liquid chromatography and bioassay for determination of ciprofloxacin in serum and urine.

机译:高压液相色谱法和生物测定法测定血清和尿液中环丙沙星的比较。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Ciprofloxacin was given orally to 10 healthy volunteers for seven consecutive doses of 250 mg every 12 h. Serum and urine samples were collected at distinct times between 0 and 96 h and analyzed both by high-pressure liquid chromatography and by a microbiological assay. The detection limits were 0.006 and 0.03 microgram/ml, respectively. For each method, imprecision coefficients of variation were less than 6.1% at various concentrations in serum and urine. The means +/- standard deviations of the absolute values of the relative differences between the two methods were 9.3 +/- 6.8% (n = 225) for serum samples and 58.5 +/- 50.4% (n = 70) for urine samples. Comparison of the concentrations in serum measured with high-pressure liquid chromatography and bioassay by regression analysis yielded a slope which was not significantly different from 1.0 (99.9% confidence limits: 0.984 less than slope less than 1.035). In urine, however, the bioassay results were markedly higher than the high-pressure liquid chromatography values (1.327 less than slope less than 1.698), which indicates the presence of antimicrobially active metabolites. The cumulative 12-h urinary recovery after the first and seventh doses averaged 30.2 +/- 8.5 and 26.4 +/- 4.6%, respectively, by high-pressure liquid chromatography, whereas with bioassay 38.2 +/- 5.9 and 45.5 +/- 5.9% activity was recovered. Protein binding appeared to be neither concentration nor pH dependent and averaged 21.9 +/- 4.1%.
机译:环丙沙星口服给予10名健康志愿者,每12小时连续服用7次,每次250 mg。在0至96小时之间的不同时间收集血清和尿液样本,并通过高压液相色谱和微生物测定法进行分析。检出限分别为0.006和0.03微克/毫升。对于每种方法,在不同浓度的血清和尿液中,不精确的变异系数均小于6.1%。两种方法之间相对差异的绝对值的均值+/-标准偏差对于血清样品为9.3 +/- 6.8%(n = 225),对于尿液样品为58.5 +/- 50.4%(n = 70)。用高压液相色谱法和生物测定法通过回归分析比较血清中的浓度,得出的斜率与1.0并无显着差异(99.9%的置信度:小于1.035的斜率小于0.984)。然而,在尿液中,生物测定结果显着高于高压液相色谱值(比斜率小于1.698小1.327),表明存在抗微生物活性代谢物。通过高压液相色谱法,第一剂和第七剂后累积的12小时尿液恢复平均分别为30.2 +/- 8.5和26.4 +/- 4.6%,而生物测定法则为38.2 +/- 5.9和45.5 +/- 5.9回收%活性。蛋白质结合似乎既不是浓度也不是pH依赖性的,平均为21.9 +/- 4.1%。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号