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血清中氨己烯酸测定的色谱方法。

Chromatographic procedures for the determination of felbamate in serum.

作者信息

Gur P, Poklis A, Saady J, Costantino A

机构信息

Department of Pathology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0165, USA.

出版信息

J Anal Toxicol. 1995 Oct;19(6):499-503. doi: 10.1093/jat/19.6.499.

Abstract

A gas-liquid chromatographic procedure and a high-performance liquid chromatographic (HPLC) procedure for the quantitative determination of the anticonvulsant drug felbamate in serum are presented. Both methods employ methyl felbamate as the internal standard. The efficiencies of felbamate extraction by both C18 solid-phase extraction (SPE) followed by HPLC and liquid-liquid extraction followed by gas chromatography (GC) were evaluated. The mean absolute recovery of felbamate over a serum concentration range of 10-100 mg/L for SPE and liquid-liquid extraction were 89.4 and 84.4%, respectively. Calibration curves for the GC and HPLC procedures were linear from 5 to 200 mg/L felbamate. The overall within-run precision of liquid-liquid extraction followed by GC analysis yielded coefficients of variation Os) of 7.3% at 16 mg/L (n = 10) and 5.8% at 100 mg/L (n = 10). The overall between-run precision for this method calculated by three determinations on a single day for three successive weeks yielded CVs of 7.8% at 16 mg/L (n = 45) and 6.3% at 100 mg/L (n = IO). The overall within-run precision of SPE followed by HPLC analysis yielded a CV of 2.9 % at 50 mg/L (n = 10), and the overall between-run precision for this method calculated by three determinations on a single day for three successive weeks yielded CVs of 3.3% at 25 mg/L (n = 40) and 3.5% at 50 mg/L (n = 37). The SPE-HPLC procedure was found to yield less variable results than the liquid-liquid-GC procedure. Limits of quantitation and detection of both methods were set at 5 mg/L felbamate. Popular anticonvulsant and acid or neutral extractable drugs did not interfere with either the GC or HPLC methods. The results of an interlaboratory, intermethod comparison study performed on patient serum specimens analyzed in one laboratory by the SPE-HPLC procedure and in another laboratory by the liquid-liquid extraction-GC procedure correlated well (r2 = 0.967; n = 41). Both methods provide clinically useful and comparable results.

摘要

本文介绍了一种用于定量测定血清中抗惊厥药物非氨酯的气-液色谱法和高效液相色谱(HPLC)法。两种方法均采用非氨酯甲酯作为内标。评估了采用C18固相萃取(SPE)后进行HPLC以及液-液萃取后进行气相色谱(GC)对非氨酯的萃取效率。对于SPE和液-液萃取,在血清浓度范围为10 - 100 mg/L时,非氨酯的平均绝对回收率分别为89.4%和84.4%。GC和HPLC方法的校准曲线在非氨酯浓度为5至200 mg/L范围内呈线性。液-液萃取后进行GC分析的总体批内精密度在16 mg/L(n = 10)时变异系数(CVs)为7.3%,在100 mg/L(n = 10)时为5.8%。通过连续三周每天进行三次测定计算得出该方法的总体批间精密度在16 mg/L(n = 45)时CV为7.8%,在100 mg/L(n = 10)时为6.3%。SPE后进行HPLC分析的总体批内精密度在50 mg/L(n = 10)时CV为2.9%,通过连续三周每天进行三次测定计算得出该方法的总体批间精密度在25 mg/L(n = 40)时CV为3.3%,在50 mg/L(n = 37)时为3.5%。发现SPE - HPLC方法比液-液 - GC方法产生的结果变异性更小。两种方法的定量限和检测限均设定为非氨酯5 mg/L。常用的抗惊厥药物以及可酸或中性萃取的药物均不干扰GC或HPLC方法。在一个实验室采用SPE - HPLC方法和在另一个实验室采用液-液萃取 - GC方法对患者血清标本进行的实验室间、方法间比较研究结果具有良好相关性(r2 = 0.967;n = 41)。两种方法均提供了临床上有用且具有可比性的结果。

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