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用于评估肾脏药物消除过程的一系列标记化合物的分析验证。

Analytical validation for a series of marker compounds used to assess renal drug elimination processes.

作者信息

McLachlan A J, Gross A S, Beal J L, Minns I, Tett S E

机构信息

Faculty of Pharmacy, The University of Sydney, St. Leonards, New South Wales, Australia.

出版信息

Ther Drug Monit. 2001 Feb;23(1):39-46. doi: 10.1097/00007691-200102000-00008.

Abstract

Renal drug elimination is determined by glomerular filtration, tubular secretion, and tubular reabsorption. Changes in the integrity of these processes influence renal drug clearance, and these changes may not be detected by conventional measures of renal function such as creatinine clearance. The aim of the current study was to examine the analytic issues needed to develop a cocktail of marker drugs (fluconazole, rac-pindolol, para-aminohippuric acid, sinistrin) to measure simultaneously the mechanisms contributing to renal clearance. High-performance liquid chromatographic methods of analysis for fluconazole, pindolol, para-aminohippuric acid, and creatinine and an enzymatic assay for sinistrin were developed or modified and then validated to allow determination of each of the compounds in both plasma and urine in the presence of all other marker drugs. A pilot clinical study in one volunteer was conducted to ensure that the assays were suitable for quantitating all the marker drugs to the sensitivity and specificity needed to allow accurate determination of individual renal clearances. The performance of all assays (plasma and urine) complied with published validation criteria. All standard curves displayed linearity over the concentration ranges required, with coefficients of correlation greater than 0.99. The precision of the interday and intraday variabilities of quality controls for each marker in plasma and urine were all less than 11.9% for each marker. Recoveries of markers (and internal standards) in plasma and urine were all at least 90%. All markers investigated were shown to be stable when plasma or urine was frozen and thawed. For all the assays developed, there were no interferences from other markers or endogenous substances. In a pilot clinical study, concentrations of all markers could be accurately and reproducibly determined for a sufficient duration of time after administration to calculate accurate renal clearance for each marker. This article presents details of the analytic techniques developed for measuring concentrations of marker drugs for different renal elimination processes administered as a single dose to define the processes contributing to renal drug elimination.

摘要

肾脏药物消除取决于肾小球滤过、肾小管分泌和肾小管重吸收。这些过程完整性的变化会影响肾脏药物清除率,而这些变化可能无法通过传统的肾功能指标如肌酐清除率检测到。本研究的目的是探讨开发一种标记药物组合(氟康唑、消旋吲哚洛尔、对氨基马尿酸、西尼地平)以同时测量影响肾脏清除率机制所需的分析问题。开发或改进了用于氟康唑、吲哚洛尔、对氨基马尿酸和肌酐的高效液相色谱分析方法以及用于西尼地平的酶法测定,然后进行验证,以允许在存在所有其他标记药物的情况下测定血浆和尿液中的每种化合物。在一名志愿者中进行了一项初步临床研究,以确保这些测定适用于定量所有标记药物,达到准确测定个体肾脏清除率所需的灵敏度和特异性。所有测定(血浆和尿液)的性能均符合已发表的验证标准。所有标准曲线在所需浓度范围内均呈线性,相关系数大于0.99。血浆和尿液中每种标记物质量控制的日间和日内变异系数均小于11.9%。血浆和尿液中标记物(和内标)的回收率均至少为90%。当血浆或尿液冷冻和解冻时,所有研究的标记物均显示稳定。对于所有开发的测定,均无来自其他标记物或内源性物质的干扰。在一项初步临床研究中,给药后在足够长的时间内可以准确且可重复地测定所有标记物的浓度,以计算每种标记物的准确肾脏清除率。本文介绍了为测量不同肾脏消除过程的标记药物浓度而开发的分析技术的详细信息,这些标记药物以单剂量给药以确定影响肾脏药物消除的过程。

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