Riley C A, Evans W E
J Chromatogr. 1986 Oct 31;382:199-205. doi: 10.1016/s0378-4347(00)83517-3.
A novel analytical methodology was developed for simultaneous high-performance liquid chromatographic quantitation of antipyrine and lorazepam in biological fluids using phenacetin and flunitrazepam as internal standards, respectively. A gradient solvent system was used to achieve specificity and sensitivity for each of the compounds in biological fluids. The between-run coefficients of variation for replicate analysis of antipyrine and lorazepam in identical plasma samples were 9.4 and 6.4% at 60 micrograms/ml and 5.5 micrograms/ml, respectively, for antipyrine, and 9.1 and 9.9% at 110 ng/ml and 10.5 ng/ml, respectively, for lorazepam. Accuracy ranged from 99.7 to 101.4% at concentrations of 8, 45 and 105 micrograms/ml for antipyrine and from 94.8 to 95.8% at concentrations of 12, 55 and 125 ng/ml for lorazepam. This method requires only one organic extraction procedure for all four compounds, allows quantitation of these two drugs in samples also containing indocyanine green, and sample throughput following extraction is totally automated.
开发了一种新型分析方法,用于同时高效液相色谱法定量生物流体中的安替比林和劳拉西泮,分别使用非那西丁和氟硝西泮作为内标。采用梯度溶剂系统以实现生物流体中每种化合物的特异性和灵敏度。相同血浆样品中安替比林和劳拉西泮重复分析的批间变异系数,安替比林在60微克/毫升和5.5微克/毫升时分别为9.4%和6.4%,劳拉西泮在110纳克/毫升和10.5纳克/毫升时分别为9.1%和9.9%。安替比林在8、45和105微克/毫升浓度下的准确度范围为99.7%至101.4%,劳拉西泮在12、55和125纳克/毫升浓度下的准确度范围为94.8%至95.8%。该方法对所有四种化合物仅需一次有机萃取程序,可对同时含有吲哚菁绿的样品中的这两种药物进行定量,且萃取后的样品通量完全自动化。