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缓释型哌甲酯的生物利用度:完整服用及将胶囊内容物撒在苹果酱上服用时高脂早餐的影响。

Bioavailability of modified-release methylphenidate: influence of high-fat breakfast when administered intact and when capsule content sprinkled on applesauce.

作者信息

Lee Lucy, Kepple Joanne, Wang Yibin, Freestone Stephen, Bakhtiar Ray, Wang Yanfeng, Hossain Mohammad

机构信息

Novartis Pharmaceuticals, East Hanover, NJ 07936, USA.

出版信息

Biopharm Drug Dispos. 2003 Sep;24(6):233-43. doi: 10.1002/bdd.358.

Abstract

Ritalin, an immediate release form of racemic methylphenidate hydrochloride, has been available in the USA since 1955 and is used for the treatment of ADHD. The objective of this study was to evaluate the pharmacokinetics of modified-release methylphenidate (highest single dose), Ritalin LA, when administered under fasting condition, with a high-fat breakfast, and when sprinkled on applesauce in healthy adult subjects. Blood samples were drawn for 24 h following a 40 mg oral administration. Most subjects appeared to produce a bimodal methylphenidate plasma concentration profile. In all three treatment groups, methylphenidate was rapidly absorbed with an initial average t(max(0-4)) of 1.3-2.4 h and an average peak plasma concentration [C(max(abs))] of 14.4-15.2 ng/ml. On average, both the rate [C(max(abs)) and t(max(abs))] and the extent of absorption (AUC(0- infinity)) of methylphenidate were similar when the capsule was given with a high fat breakfast and when the capsule contents were sprinkled onto applesauce, compared with the fasting state. No dose dumping was observed when the capsule was given with a high fat breakfast or when sprinkled onto applesauce. The dose was safe and generally well tolerated. Coadministration of a single oral dose of 40 mg methylphenidate capsule whether administered intact with a high-fat breakfast or sprinkled on applesauce did not affect the overall rate or extent of absorption of methylphenidate compared with the fasted condition.

摘要

利他林是消旋盐酸哌甲酯的速释剂型,自1955年起在美国上市,用于治疗注意力缺陷多动障碍(ADHD)。本研究的目的是评估在禁食状态下、搭配高脂早餐服用以及撒在苹果酱上时,缓释哌甲酯(最高单次剂量,即利他林长效制剂)在健康成年受试者体内的药代动力学。口服40毫克后采集24小时血样。大多数受试者的哌甲酯血浆浓度曲线呈现双峰。在所有三个治疗组中,哌甲酯吸收迅速,初始平均达峰时间[t(max(0 - 4))]为1.3 - 2.4小时,平均血浆峰浓度[C(max(abs))]为14.4 - 15.2纳克/毫升。与禁食状态相比,当胶囊与高脂早餐一起服用以及将胶囊内容物撒在苹果酱上时,哌甲酯的吸收速率[C(max(abs))和t(max(abs))]和吸收程度(AUC(0 - ∞))平均相似。当胶囊与高脂早餐一起服用或撒在苹果酱上时,未观察到剂量倾泻现象。该剂量安全且一般耐受性良好。与禁食状态相比,单次口服40毫克哌甲酯胶囊,无论是完整地与高脂早餐一起服用还是撒在苹果酱上,均不影响哌甲酯的总体吸收速率或程度。

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