Jennison T A, Brown P, Crossett J, Kushnir M, Urry F M
Associated Regional and University Pathologists, Inc., Salt Lake City, UT 84108, USA.
J Anal Toxicol. 1995 Nov-Dec;19(7):537-41. doi: 10.1093/jat/19.7.537.
A gas chromatographic method using nitrogen-phosphorus detection was developed to quantitate clozapine in plasma or serum. Methyl clonazepam was used as an internal standard. Sample preparation included a single-step extraction with ethyl acetate, which was injected directly onto a wide-bore capillary column. Within-run and total precision, measured as percent coefficient of variation, were determined at low, therapeutic, and high clozapine plasma concentrations. The within-run precision for the low, therapeutic, and high clozapine plasma samples was 5.2, 2.7, and 2.4%, respectively. The total precision for the low, therapeutic, and high clozapine plasma samples was 10.0, 2.6, and 2.0%, respectively. Analytical accuracy was evaluated by comparing quantitative results with those obtained from a reference laboratory. Those samples containing therapeutic or high concentrations agreed within 3%; the sample containing a subtherapeutic concentration differed by 11.9%. The limit of quantitation was determined to be 35 ng/mL, and the upper limit of linearity was 3000 ng/mL. No significant interferences were detected after testing more than two dozen drugs and metabolites.
建立了一种使用氮磷检测的气相色谱法来定量测定血浆或血清中的氯氮平。甲基氯硝西泮用作内标。样品制备包括用乙酸乙酯进行单步萃取,然后直接注入大口径毛细管柱。在低、治疗和高氯氮平血浆浓度下,以内标变异系数百分比衡量的批内精密度和总精密度得以确定。低、治疗和高氯氮平血浆样品的批内精密度分别为5.2%、2.7%和2.4%。低、治疗和高氯氮平血浆样品的总精密度分别为10.0%、2.6%和2.0%。通过将定量结果与参考实验室获得的结果进行比较来评估分析准确性。那些含有治疗浓度或高浓度的样品在3%以内相符;含有亚治疗浓度的样品相差11.9%。定量限确定为35 ng/mL,线性上限为3000 ng/mL。在检测了二十多种药物和代谢物后,未检测到明显干扰。