Yu D K, Williams R L, Benet L Z, Lin E T, Giesing D H
Biopharmaceutics Department, Marion Laboratories, Kansas City, Missouri 64137.
Biopharm Drug Dispos. 1988 Nov-Dec;9(6):557-65. doi: 10.1002/bod.2510090606.
Single dose oral nitroglycerin (GTN) was administered to six healthy subjects as 6.5, 9.0, and 13.0 mg aqueous solutions in sequential study phases to characterize the oral pharmacokinetics of GTN and the dinitrate metabolites. Blood samples were collected periodically up to 10 h. Plasma concentrations of GTN were measurable in some subjects up to 1/2 and 1 h, respectively, after the 9.0 and 13.0 mg dose. The mean GTN Cmax values of the three solution doses were 0.28, 0.78, and 0.42 ng ml-1 in ascending dosage. The erratic nature of GTN plasma profiles prevented meaningful pharmacokinetic analysis, although tmax was consistently 5 min. In all three treatments, both GTN metabolites (1,2- and 1,3-glyceryldinitrates, GDNs) peaked at about 20 min, followed by a distributive phase and a log-linear decline in concentrations. Terminal half-lives for both GDNs were approximately 50 min in all three doses. The plasma concentrations of the metabolites were higher than nitroglycerin with 1,2-GDN exhibiting the highest overall profile.
在连续的研究阶段,对6名健康受试者分别给予6.5毫克、9.0毫克和13.0毫克的单剂量口服硝酸甘油(GTN)水溶液,以表征GTN及其二硝酸盐代谢产物的口服药代动力学。在长达10小时的时间内定期采集血样。在服用9.0毫克和13.0毫克剂量后,分别在长达1/2小时和1小时内,部分受试者的血浆GTN浓度可测。三个溶液剂量的GTN平均Cmax值随剂量增加依次为0.28、0.78和0.42纳克/毫升。尽管tmax始终为5分钟,但GTN血浆曲线的不稳定性妨碍了有意义的药代动力学分析。在所有三种治疗中,两种GTN代谢产物(1,2-和1,3-甘油二硝酸盐,GDNs)均在约20分钟时达到峰值,随后进入分布相,浓度呈对数线性下降。在所有三个剂量下,两种GDNs的终末半衰期约为50分钟。代谢产物的血浆浓度高于硝酸甘油,其中1,2-GDN的总体水平最高。