Hussain Y, Güzelhan C, Odink J, van der Beek E J, Hartmann D
Pharma Clinical Research, F. Hoffmann-La Roche, Ltd. Basel, Switzerland.
J Clin Pharmacol. 1994 Nov;34(11):1121-5. doi: 10.1002/j.1552-4604.1994.tb01990.x.
Orlistat is a potent and selective inhibitor of gastrointestinal lipases. The drug is designed for the treatment of obesity. The effect on dietary fat absorption of orlistat after administration of divided doses spread over 2 hours from mid-meal, in comparison with that after administration of a full dose mid-meal, was investigated in a randomized, single-blind study including 16 hospitalized healthy males. After a 5-day run-in, to accustom the subjects to a diet of 2350 kcal and 76 g fat per day and to establish baseline fecal fat excretion, subjects received, in two parallel groups of eight over 8 days, three times a day 80 mg orlistat at mid-meal, and placebo at mid-meal and 0.5, 1, and 2 hr after mid-meal (group A), or placebo at mid-meal, and 20 mg orlistat at mid-meal and 0.5, 1, and 2 hr after mid-meal (group B). Feces were collected to measure total fat excretion. The mean (SD) of fecal fat in percent of dietary fat, after deduction of pretreatment fecal fat, was (%) 36.1 (4.2) and 37.0 (9.3) in groups A and B, respectively. Changing the mode of administration of orlistat, within the dose regimens investigated, does not affect its pharmacologic efficacy.
奥利司他是一种强效且具有选择性的胃肠道脂肪酶抑制剂。该药物用于治疗肥胖症。在一项包括16名住院健康男性的随机、单盲研究中,研究了从餐中开始分剂量在2小时内给药的奥利司他与餐中给予全剂量后对饮食中脂肪吸收的影响。经过5天的导入期,为使受试者适应每天2350千卡热量和76克脂肪的饮食并建立粪便脂肪排泄基线,在8天内将受试者分为两组,每组8人,一组在餐中每天三次服用80毫克奥利司他,餐中及餐后0.5、1和2小时服用安慰剂(A组),另一组餐中服用安慰剂,餐中及餐后0.5、1和2小时服用20毫克奥利司他(B组)。收集粪便以测量总脂肪排泄量。扣除预处理粪便脂肪后,A组和B组粪便脂肪占饮食脂肪的百分比均值(标准差)分别为(%)36.1(4.2)和37.0(9.3)。在所研究的剂量方案范围内,改变奥利司他的给药方式不会影响其药理疗效。