Ohnishi A, Mihara M, Kamakura H, Tomono Y, Hasegawa J, Yamazaki K, Morishita N, Tanaka T
Department of Internal Medicine, Daisan Hospital, Jikei University School of Medicine, Tokyo, Japan.
J Clin Pharmacol. 1993 Nov;33(11):1086-91. doi: 10.1002/j.1552-4604.1993.tb01945.x.
E2020, a central-acting cholinesterase inhibitor, is now under clinical development as a potential therapeutic agent for senile dementia of Alzheimer type. In the current study, the authors compared the pharmacokinetics of this drug after single oral administration in 12 healthy young volunteers (20-27 years of age) and 6 elderly volunteers (65-82 years of age). The subjects received a single 2-mg oral dose of E2020 after a meal. Blood samples for determination of the drug level were collected over 168 hours after drug administration and were measured by specific high-pressure liquid chromatography methods with ultraviolet detection. E2020 was generally well tolerated by all subjects of both groups. The plasma elimination half-life of the beta-phase (t 1/2 beta) and time to maximum peak plasma concentration (tmax) were significantly longer in the elderly than in the young: t 1/2 beta, 103.8 +/- 40.6 versus 59.7 +/- 16.1 hours; and tmax, 5.2 +/- 2.8 versus 3.4 +/- 1.5 hours, respectively. There were no statistically significant differences in maximum peak plasma concentration and area under the curve between the two groups. The mean (+/- standard deviation) oral clearance (Cl/F) in the elderly (9.1 +/- 2.4 L/h) was similar to that in the young (10.6 +/- 2.7 L/h). The volume of distribution in the steady state (Vdss/F) was significantly larger in the elderly than that in the young: 1217.2 +/- 223.2 versus 852.5 +/- 147.7 L, respectively. These results suggested that the drug was absorbed more slowly and distributed more widely and thoroughly, but that its clearance from the body is essentially unaffected by age.(ABSTRACT TRUNCATED AT 250 WORDS)
E2020是一种中枢作用的胆碱酯酶抑制剂,目前正作为治疗阿尔茨海默型老年痴呆症的潜在治疗药物进行临床开发。在当前研究中,作者比较了该药物在12名健康年轻志愿者(20 - 27岁)和6名老年志愿者(65 - 82岁)单次口服给药后的药代动力学。受试者餐后单次口服2毫克E2020。给药后168小时内采集用于测定药物水平的血样,并通过具有紫外检测的特定高压液相色谱法进行测量。两组所有受试者对E2020总体耐受性良好。老年组β相的血浆消除半衰期(t 1/2β)和达到最大血浆峰浓度的时间(tmax)明显长于年轻组:t 1/2β分别为103.8±40.6小时和59.7±16.1小时;tmax分别为5.2±2.8小时和3.4±1.5小时。两组之间的最大血浆峰浓度和曲线下面积无统计学显著差异。老年组的平均(±标准差)口服清除率(Cl/F)(9.1±2.4 L/h)与年轻组(10.6±2.7 L/h)相似。老年组稳态分布容积(Vdss/F)明显大于年轻组:分别为1217.2±223.2升和852.5±147.7升。这些结果表明,该药物吸收更慢,分布更广泛且更彻底,但它从体内的清除基本不受年龄影响。(摘要截断于250字)