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首页> 外文期刊>Journal of pharmaceutical sciences. >Simultaneous determination of BNP7787 and its metabolite mesna in plasma and tissue by micro-HPLC with a dual electrochemical detector.
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Simultaneous determination of BNP7787 and its metabolite mesna in plasma and tissue by micro-HPLC with a dual electrochemical detector.

机译:采用双电化学检测器的微型HPLC同时测定血浆和组织中的BNP7787及其代谢产物黑素。

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摘要

Sensitive, accurate, and precise assays are described to determine BNP7787 (disodium 2,2'-dithio-bis-ethane sulfonate) and its metabolite mesna (sodium 2-mercaptoethane sulfonate) simultaneously in plasma and tissue by micro-high-performance liquid chromatography (HPLC) with dual electrochemical detection. After separation of BNP7787 and mesna by micro-HPLC, the disulfide BNP7787 was reduced to mesna by a reactor cell with a glassy carbon working electrode (-1.6 V versus Hy-REF). At the second electrode, which consisted of a gold wall-jet electrode, the mesna generated from BNP7787 and the mesna already present in the samples were detected (+0.85 V versus Ag/AgCl). The lower limit of quantification (LLQ) of both compounds was 3 microM in plasma and 20 nmol/g in tissue. The dynamic range of the assay in plasma was 3-120 microM for mesna and 15-1200 microM for BNP7787. In tissue, the dynamic range was 20-2000 nmol/g for both compounds. The recovery of mesna from plasma and tissue ranged from 61.4 to 90.5% and 82.7 to 90.2%, respectively, and seemed to be concentration dependent. The recovery of BNP7787 from plasma and tissue was complete (i.e., 101.5 and 96.4%, respectively). The within- and between-day accuracy and precision for the plasma and tissue assay were within 14 and 7%, respectively. The utility of the assay was shown by determination of the stability of mesna and BNP7787 in a kidney sample of a rat and by analysis of plasma samples obtained from a patient receiving 18.4 g/m(2) BNP7787 as a 15-min intravenous infusion.
机译:描述了灵敏,准确和精确的测定方法,可通过微高效液相色谱法同时测定血浆和组织中的BNP7787(2,2'-二硫代双乙烷磺酸二钠)及其代谢产物mesna(2-巯基乙磺酸钠) (HPLC)具有双重电化学检测。通过微量HPLC分离BNP7787和甲基萘后,通过带有玻璃碳工作电极(-Hy-REF为-1.6 V)的反应池将二硫化物BNP7787还原为甲基萘。在由金壁喷射电极组成的第二电极上,检测到由BNP7787生成的膜和样品中已经存在的膜(+0.85 V,相对于Ag / AgCl)。两种化合物的定量下限(LLQ)在血浆中均为3 microM,在组织中为20 nmol / g。血浆中测定的动态范围对于mesna为3-120 microM,对于BNP7787为15-1200 microM。在组织中,两种化合物的动态范围均为20-2000 nmol / g。从血浆和组织中恢复mesna的范围分别为61.4%至90.5%和82.7%至90.2%,并且似乎是浓度依赖性的。 BNP7787从血浆和组织中的回收已完成(分别为101.5%和96.4%)。血浆和组织测定的日内和日间准确度和精密度分别在14%和7%之内。通过测定大鼠肾脏样品中mesna和BNP7787的稳定性,并通过分析从接受18.4 g / m(2)BNP7787的患者获得的血浆样品中获得的血浆样品进行15分钟静脉内输注,可以显示该测定法的实用性。

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