Lin W, Kelly A R
Ther Drug Monit. 1985;7(3):336-43. doi: 10.1097/00007691-198507030-00019.
A simple, fast, sensitive, and inexpensive method is described for routine therapeutic monitoring of both total and free valproic acid (VPA) at therapeutic concentrations in seizure patients. The method uses solid-phase (Bond Elut) columns for the preliminary extraction of 100 microliters plasma or serum and gas-liquid chromatography (GLC) analysis, using 10% Carbowax 6000 on a Chromosorb WAW 80/100 column and alpha-methyl-alpha-ethylcaproic acid as an internal standard. The extraction efficiency for VPA at a concentration of 70 micrograms/ml is 98 +/- 4%. The calibration curve is linear in the range of 1.0-280 microliters/ml. The detection limit of VPA is 1.0 micrograms/ml. Syva enzyme multiplied immunoassay technique (EMIT) Free-Level filters were used in the analysis of free VPA from plasma. The described Bond Elut X GLC (BE X GLC) method was used to determine total drug concentrations in 56 VPA-treated patients, and the results were compared with those obtained by conventional liquid-liquid extraction X GLC analysis. The 44 sera involved were also analyzed by EMIT. In addition, BE X GLC was compared with the Abbott TDx system on an additional 21 specimens. Statistical agreement was excellent between BE X GLC and TDx, but poor between BE X GLC and liquid-liquid extraction X GLC. Agreement with the EMIT method was intermediate.
本文描述了一种简单、快速、灵敏且经济的方法,用于对癫痫患者治疗浓度下的总丙戊酸(VPA)和游离丙戊酸进行常规治疗监测。该方法使用固相(Bond Elut)柱对100微升血浆或血清进行初步萃取,然后采用气液色谱(GLC)分析,在Chromosorb WAW 80/100柱上使用10%的聚乙二醇6000,并以α-甲基-α-乙基己酸作为内标。VPA在浓度为70微克/毫升时的萃取效率为98±4%。校准曲线在1.0 - 280微克/毫升范围内呈线性。VPA的检测限为1.0微克/毫升。在分析血浆中的游离VPA时使用了Syva酶放大免疫分析技术(EMIT)游离水平过滤器。所描述的Bond Elut X GLC(BE X GLC)方法用于测定56例接受VPA治疗患者的总药物浓度,并将结果与通过传统液 - 液萃取X GLC分析获得的结果进行比较。对所涉及的44份血清也采用EMIT进行了分析。此外,在另外21个样本上对BE X GLC与雅培TDx系统进行了比较。BE X GLC与TDx之间的统计学一致性极佳,但BE X GLC与液 - 液萃取X GLC之间的一致性较差。与EMIT方法的一致性处于中等水平。