McCormick S R, Nielsen J, Jatlow P
Clin Chem. 1984 Oct;30(10):1652-5.
A reversed-phase "high-performance" liquid-chromatographic assay for the quantification of alprazolam in serum or plasma is described. Serum or plasma is extracted with toluene/isoamyl alcohol (99/1 by vol), evaporated, and reconstituted in the mobile phase. The latter is washed with hexane, then subjected to reversed-phase liquid chromatography and ultraviolet detection at 202 nm. Either U-31485, an alprazolam analog, or lorazepam, a 3-hydroxybenzodiazepine, is satisfactory as internal standards. Major alprazolam metabolites and various other commonly used drugs do not interfere. The useful lower limit of sensitivity for quantification is 2.5 micrograms/L. Peak height and alprazolam concentration are linearly related from 2.5 to 100 micrograms/L. For 10 and 20 micrograms/L concentrations, within-run CVs were 1.4% and 0.9% and the between-runs CVs 4.8% and 3.2%. Steady-state serum concentrations ranged from 25 to 55 micrograms/L in patients taking 1.5 to 6.0 mg per day, orally. Preliminary data suggest the method is also suitable for analysis of the structurally similar triazolobenzodiazepine, triazolam.
本文描述了一种用于定量测定血清或血浆中阿普唑仑的反相“高效”液相色谱法。血清或血浆用甲苯/异戊醇(体积比99/1)萃取,蒸发后,再用流动相复溶。流动相先用己烷洗涤,然后进行反相液相色谱分析,并在202nm处进行紫外检测。阿普唑仑类似物U - 31485或3 - 羟基苯二氮䓬类药物劳拉西泮作为内标均令人满意。阿普唑仑的主要代谢产物和各种其他常用药物均不产生干扰。定量分析的有效灵敏度下限为2.5微克/升。峰高与阿普唑仑浓度在2.5至100微克/升范围内呈线性关系。对于10微克/升和20微克/升的浓度,批内变异系数分别为1.4%和0.9%,批间变异系数分别为4.8%和3.2%。口服每日1.5至6.0毫克的患者,稳态血清浓度范围为25至55微克/升。初步数据表明该方法也适用于分析结构相似的三唑并苯二氮䓬类药物三唑仑。