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将用于茶碱、苯巴比妥、苯妥英、卡马西平、扑米酮、乙琥胺和庆大霉素的微量体积酶放大免疫测定法适配至CentrifiChem化学分析仪。

Adaptation of microvolume EMIT assays for theophylline, phenobarbital, phenytoin, carbamazepine, primidone, ethosuximide, and gentamicin to a CentrifiChem chemistry analyzer.

作者信息

Studts D, Haven G T, Kiser E J

出版信息

Ther Drug Monit. 1983;5(3):335-40. doi: 10.1097/00007691-198309000-00016.

Abstract

We have developed microvolume EMIT procedures for theophylline, phenobarbital, phenytoin, carbamazepine, primidone, ethosuximide, and gentamicin using a centrifugal analyzer (CentrifiChem and Pipettor 1000) to reduce the manufacturer's recommended manual reagent consumption by one-sixth. In addition to developing the EMIT procedure, the performance of the analyzer and pipettor were verified. The analyzer and pipettor are capable of producing within-run precision at a 3-microliters sample volume and 210-microliters analyzer cuvette volume equal to or less than 1.5%. The performance of the EMIT procedures on the analyzer yielded spike drug recoveries of 90.8 to 106.1% for drug concentrations throughout the calibration concentration range of each assay. The percent error on standard reference material of the National Bureau of Standards ranged from a +12.0% to a -0.6% for ethosuximide, phenobarbital, phenytoin, and primidone. Patient comparison data yielded slopes from 0.930 to 1.110 for all assays. The other important feature of the adapted EMIT assay is its simplicity for use on a routine basis.

摘要

我们使用离心分析仪(CentrifiChem和Pipettor 1000)开发了针对茶碱、苯巴比妥、苯妥英、卡马西平、扑米酮、乙琥胺和庆大霉素的微量体积酶放大免疫测定技术(EMIT)程序,将制造商推荐的手工试剂消耗量减少了六分之一。除了开发EMIT程序外,还对分析仪和移液器的性能进行了验证。该分析仪和移液器在3微升样品体积和210微升分析仪比色杯体积下能够产生的批内精密度等于或小于1.5%。分析仪上EMIT程序的性能在每个测定的校准浓度范围内,药物浓度的加标药物回收率为90.8%至106.1%。对于乙琥胺、苯巴比妥、苯妥英和扑米酮,国家标准局标准参考物质的百分误差范围为+12.0%至 -0.6%。患者比较数据显示,所有测定的斜率为0.930至1.110。改进后的EMIT测定法的另一个重要特点是其在常规使用时的简便性。

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