Sadée W, Staroscik J, Finn C, Cohen J
J Pharm Sci. 1975 Jun;64(6):998-1001. doi: 10.1002/jps.2600640623.
Specific assay procedures were developed to measure plasma concentrations of (plus or minus)-1, 2-bis(3, 5-dioxopiperazinyl) propane (1) by GLC using flame-ionization detection with a sensitivity limit of 5 mug/ml and by GLC-mass fragmentography with a sensitivity limit of 0.2 mug/ml. Applicability of the assay procedures was demonstrated in rats, rabbits, and humans. Plasma concentration-time curves of total 14-C activity and intact I was obtained in rats and rabbits following oral and intravenous administration of 14-C-I. Plasma elimination half-lives of I in the first 2 hr following intravenous doses in rats were 40 and 45 min in two rats. Plasma levels of I were measured over 6 hr after an intravenous dose in rabbits and followed a two-compartment open model with a terminal loglinear plasma half-life of 85 min. Significantly higher total 14-C levels compared to intact I plasma concentrations indicated rapid biotransformation in both rats and rabbits to unknown metabolites. The oral bioavailability appeared to be limited in both species relative to intravenous administration. Two patients receiving 3 g I/m-2 in tablets orally showed plasma levels of I similar to those obtained after oral doses in rats and rabbits, with peak concentrations at 2 hr after the dose (3.8 mug/ml) and with still measurable levels 12 hr after the dose (0.4 mug/ml).
已开发出特定的分析程序,通过使用火焰离子化检测的气相色谱法(GLC)测定(±)-1,2-双(3,5-二氧代哌嗪基)丙烷(1)的血浆浓度,其灵敏度极限为5微克/毫升,以及通过灵敏度极限为0.2微克/毫升的气相色谱-质谱碎片分析法。该分析程序在大鼠、兔子和人类身上得到了验证。在大鼠和兔子口服和静脉注射14-C-1后,获得了总14-C活性和完整的1的血浆浓度-时间曲线。在两只大鼠中,静脉注射剂量后最初2小时内1的血浆消除半衰期分别为40分钟和45分钟。在兔子静脉注射剂量后6小时内测量了1的血浆水平,其遵循二室开放模型,终末对数线性血浆半衰期为85分钟。与完整的1血浆浓度相比,总14-C水平显著更高,表明在大鼠和兔子中1均迅速生物转化为未知代谢物。相对于静脉给药,两种物种的口服生物利用度似乎都有限。两名口服片剂形式的3克1/平方米的患者,其1的血浆水平与大鼠和兔子口服剂量后获得的水平相似,给药后2小时达到峰值浓度(3.8微克/毫升),给药后12小时仍可测量到水平(0.4微克/毫升)。