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健康志愿者连续10天重复给药后纯化分离的绿茶儿茶素表没食子儿茶素没食子酸酯(EGCG)的血浆动力学特征。

Plasma-kinetic characteristics of purified and isolated green tea catechin epigallocatechin gallate (EGCG) after 10 days repeated dosing in healthy volunteers.

作者信息

Ullmann U, Haller J, Decourt J D, Girault J, Spitzer V, Weber P

机构信息

Roche Vitamins Ltd, Human Nutrition and Health, Research and Development, Basel, Switzerland.

出版信息

Int J Vitam Nutr Res. 2004 Jul;74(4):269-78. doi: 10.1024/0300-9831.74.4.269.

Abstract

This randomized, double-blind, placebo-controlled study assessed the safety, tolerability, and plasma-kinetic behavior of 94% pure crystalline epigallocatechin gallate (EGCG) after ten days' repeated dosing in 36 healthy male volunteers. Each of the three treatment groups consisted of 12 subjects; nine of them received oral EGCG in one dose of 200, 400, or 800 mg daily, and three received a placebo. Blood samples for plasma-kinetic EGCG characterization were taken on day 1 and day 10. Kinetic parameters for rate and extent, elimination half-lives, and accumulation factor (R) were determined and compared between day 1 and day 10 for each dosage group. Orally administered EGCG is rapidly absorbed from the gut. Dose linearity was applied for single-dose application (day 1). After repeated dosing (day 10) dose linearity was applied between the 200 mg and 400 mg group. Dose escalation to 800 mg was more than dose-proportional in rate and extent, and statistically different from the 200 mg and 400 mg group. An increase in elimination half-life (t1/2.z) and in the accumulation factor (R) in the 800 mg dosage group indicates dose-dependent saturation of capacity-limited excretion routes or an increase of hepato-duodenal re-circulation. Ten days' repeated administration of oral doses of EGCG of up to 800 mg per day were found to be safe and very well tolerated.

摘要

这项随机、双盲、安慰剂对照研究评估了94%纯度的结晶表没食子儿茶素没食子酸酯(EGCG)在36名健康男性志愿者中连续10天重复给药后的安全性、耐受性和血浆动力学行为。三个治疗组每组12名受试者;其中9人每天口服一次200、400或800毫克的EGCG,3人服用安慰剂。在第1天和第10天采集血样用于血浆动力学EGCG特征分析。测定每个剂量组在第1天和第10天的速率和程度、消除半衰期和蓄积因子(R)的动力学参数并进行比较。口服EGCG可迅速从肠道吸收。单剂量给药(第1天)呈剂量线性关系。重复给药(第10天)后,200毫克和400毫克组之间呈剂量线性关系。剂量增至800毫克时,速率和程度的增加超过剂量比例,且与200毫克和400毫克组有统计学差异。800毫克剂量组的消除半衰期(t1/2.z)和蓄积因子(R)增加表明容量限制排泄途径的剂量依赖性饱和或肝十二指肠再循环增加。每天口服高达800毫克的EGCG连续给药10天被发现是安全的,且耐受性良好。

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