Fowles S E, Pierce D M
Analyst. 1989 Nov;114(11):1373-5. doi: 10.1039/an9891401373.
A rapid, sensitive and reliable reversed-phase high-performance liquid chromatographic (HPLC) method with UV detection has been developed for the assay of a novel anti-herpes agent, 9-(4-hydroxy-3-hydroxymethylbut-1-yl)guanine (BRL-39123), in human plasma and urine. The drug and the internal standard, the structural analogue BRL-42377, were extracted from the biological matrix by adsorption on a cation-exchange column and were subsequently eluted under alkaline conditions prior to HPLC. The method is reproducible, with coefficients of variation of ca. 5%, and linear from 0.1 to at least 30 micrograms ml-1 in plasma and from 50 to at least 2000 micrograms ml-1 in urine. The method has been used extensively to measure BRL-39123 in plasma and urine samples generated during clinical studies and is adequate for defining pharmacokinetics at projected therapeutic doses.
已开发出一种快速、灵敏且可靠的反相高效液相色谱(HPLC)法,并采用紫外检测,用于测定新型抗疱疹药物9-(4-羟基-3-羟甲基丁-1-基)鸟嘌呤(BRL-39123)在人血浆和尿液中的含量。药物及其内标物(结构类似物BRL-42377)通过吸附在阳离子交换柱上从生物基质中提取出来,随后在碱性条件下洗脱,再进行HPLC分析。该方法具有可重复性,变异系数约为5%,在血浆中浓度范围为0.1至至少30微克/毫升,在尿液中为50至至少2000微克/毫升时呈线性。该方法已广泛用于测定临床研究期间采集的血浆和尿液样本中的BRL-39123,足以确定预计治疗剂量下的药代动力学。