Jochemsen R, van Rijn P A, Hazelzet T G, van Boxtel C J, Breimer D D
Biopharm Drug Dispos. 1986 Jan-Feb;7(1):53-61. doi: 10.1002/bdd.2510070108.
The pharmacokinetics of oral midazolam (Dormicum, 15 mg) and loprazolam (Dormonoct, 1 mg) were studied in eight healthy young volunteers in a cross-over design. Plasma concentrations of midazolam were measured with a gas chromatographic method and loprazolam concentrations were determined by a radio-receptor technique. Absorption of midazolam proceeded very rapidly (median tmax = 0.4 h) and a rapid onset of sedative action was observed. Loprazolam absorption was relatively slow (median tmax = 3 h) and its absorption profile was often irregular. Most subjects fell asleep before peak concentrations were reached. Median peak concentrations were 94 ng ml-1 and 3.1 ng ml-1 for midazolam and loprozolam, respectively. The median elimination half-life of midazolam was 1.8 h and that of loprazolam 15 h. It is possible that the elimination half-life of loprazolam as determined by radioreceptor assay is determined by active metabolites rather than by loprazolam itself. Midazolam elimination half-life was the same when determined by radioreceptor assay or by GLC. There was no significant correlation between the half-lives of the two drugs.
采用交叉设计,在8名健康年轻志愿者中研究了口服咪达唑仑(多美康,15毫克)和氯普唑仑(多眠新,1毫克)的药代动力学。用气相色谱法测定咪达唑仑的血浆浓度,用放射受体技术测定氯普唑仑的浓度。咪达唑仑吸收非常迅速(中位达峰时间=0.4小时),并观察到镇静作用迅速起效。氯普唑仑吸收相对较慢(中位达峰时间=3小时),其吸收曲线常不规则。大多数受试者在达到峰浓度之前就入睡了。咪达唑仑和氯普唑仑的中位峰浓度分别为94纳克/毫升和3.1纳克/毫升。咪达唑仑的中位消除半衰期为1.8小时,氯普唑仑为15小时。通过放射受体测定法测定的氯普唑仑消除半衰期可能由活性代谢物而非氯普唑仑本身决定。通过放射受体测定法或气相色谱法测定时,咪达唑仑的消除半衰期相同。两种药物的半衰期之间无显著相关性。