血浆中安替比林的分光光度测定:再评价。

D J Greenblatt, A Locniskar
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引用次数: 0

摘要

重新评价了分光光度法测定安替比林的线性、灵敏度和可重复性。无论在水、稀酸或血浆中制备,当浓度至少为50微克/毫升时,标准曲线始终呈线性。对健康人的敏感限度为每毫升血浆1至2微克安替比林。相同样品的日内变异系数从2微克/毫升时的12.3%到50微克/毫升时的1.2%不等。相同样品间隔两年的平均偏差为3.8%,表明在-20℃下长时间储存期间具有较高的日间可重复性和稳定性。因此,分光光度法测定安替比林适用于大多数临床药代动力学研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectrophotometric assay of antipyrine in plasma: a reevaluation.

The linearity, sensitivity, and replicability of the spectrophotometric antipyrine assay were reevaluated. Standard curves are always linear through concentrations of at least 50 microgram/ml, whether prepared in water, dilute acid, or plasma. Sensitivity limits are 1 to 2 microgram of antipyrine per ml of plasma in healthy individuals. Within-day coefficients of variation for identical samples ranged from 12.3% at 2 microgram/ml to 1.2% at 50 microgram/ml. Identical samples assayed two years apart deviated by a mean of 3.8%, indicating high between-day replicability as well as stability during prolonged storage at -20 degrees C. Thus the spectrophotometric assay for antipyrine is suitable for most clinical pharmacokinetic studies.

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