Clark C R, Krieger R I, Miller J L
Pharmacology. 1978;17(2):98-103. doi: 10.1159/000136841.
6 male rhesus monkeys (Macaca mulatta) were treated with 14CH3-N-antipyrine (15 mg/kg, i.v.). Antipyrine plasma half-lives (APH) were determined using HSLC, radiometric, and spectrophotometric methods. APHs obtained by HSLC analysis of plasma extracts were lower than radiometric and spectrophotometric determinations. The three procedures were investigated to determine if coextraction of metabolites might be responsible for differences in APH. All three solvent systems extract significant quantities of antipyrine metabolites. N-desmethylantipyrine and 3-hydroxymethylantipyrine may interfere with spectrophotometric determination of antipyrine. While all three methods are capable of detecting changes in hepatic oxidative metabolism, HSLC permits direct measurement of antipyrine concentrations and APH.
6只雄性恒河猴(猕猴)接受了14C标记的N-安替比林(15毫克/千克,静脉注射)治疗。使用高效液相色谱法(HSLC)、放射性测定法和分光光度法测定安替比林的血浆半衰期(APH)。通过对血浆提取物进行HSLC分析得到的APH低于放射性测定法和分光光度法的测定结果。对这三种方法进行了研究,以确定代谢物的共提取是否可能是APH差异的原因。所有三种溶剂系统都能提取大量的安替比林代谢物。N-去甲基安替比林和3-羟甲基安替比林可能会干扰安替比林的分光光度测定。虽然这三种方法都能够检测肝脏氧化代谢的变化,但HSLC可以直接测量安替比林浓度和APH。