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采用反相高效液相色谱法测定活性来氟米特代谢物(A77 1726)。

Measurement of the active leflunomide metabolite (A77 1726) by reverse-phase high-performance liquid chromatography.

作者信息

Dias V C, Lucien J, LeGatt D F, Yatscoff R W

机构信息

Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Canada.

出版信息

Ther Drug Monit. 1995 Feb;17(1):84-8. doi: 10.1097/00007691-199502000-00014.

DOI:10.1097/00007691-199502000-00014
PMID:7725383
Abstract

The immunosuppressive activity of leflunomide is expressed after conversion to its pharmacologically active metabolite A77 1726. Leflunomide is a potent immunosuppressant that inhibits both T-cell and B-cell activity. To date, no pharmacokinetic data have been reported on leflunomide or A77 1726, primarily because of lack of a suitable method for its analysis. We describe here the development and evaluation of a reverse-phase high-performance liquid chromatographic (HPLC) method for the analysis of A77 1726 in whole blood or plasma from humans or rabbits. In human blood, the method exhibited good analytic recoveries from 78 +/- 13.5% to 108 +/- 4.8% (mean +/- SD) for drug concentrations ranging from 400 to 100,000 micrograms/L. When using a sample volume of 0.25 ml the sensitivity of the method was found to be 400 micrograms/L, with a working standard range of up to 200,000 micrograms/L. The sensitivity of the method can be increased to 40 micrograms/L when 1.0 ml of sample is used. Between-run coefficients of variation of 12.2 and 14.7% at A77 1726 mean concentrations of 1,006 and 8,146 micrograms/L were found for this method. No significant differences in recovery of drug were noted when either human or rabbit plasma or whole blood was used as the medium of analysis. In whole-blood specimens, A77 1726 was found to be stable for up to 10 days at -20 or -70 degrees C.

摘要

来氟米特的免疫抑制活性在转化为其药理活性代谢产物A77 1726后得以体现。来氟米特是一种强效免疫抑制剂,可抑制T细胞和B细胞活性。迄今为止,尚未有关于来氟米特或A77 1726的药代动力学数据报道,主要原因是缺乏合适的分析方法。我们在此描述一种反相高效液相色谱(HPLC)方法的开发与评估,用于分析人或兔全血或血浆中的A77 1726。在人血中,对于浓度范围为400至100,000微克/升的药物,该方法的分析回收率在78±13.5%至108±4.8%(平均值±标准差)之间。当使用0.25毫升样品体积时,该方法的灵敏度为400微克/升,工作标准范围高达200,000微克/升。当使用1.0毫升样品时,该方法的灵敏度可提高到40微克/升。该方法在A77 1726平均浓度为1,006和8,146微克/升时,批间变异系数分别为12.2%和14.7%。当使用人或兔血浆或全血作为分析介质时,未观察到药物回收率有显著差异。在全血标本中,发现A77 1726在-20或-70℃下可稳定保存长达10天。

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Ther Drug Monit. 1995 Feb;17(1):84-8. doi: 10.1097/00007691-199502000-00014.
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