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基于对人类志愿者胃肠道转运的闪烁扫描监测预测口服茶碱的血药浓度-时间曲线

Prediction of plasma concentration-time curve of orally administered theophylline based on a scintigraphic monitoring of gastrointestinal transit in human volunteers.

作者信息

Haruta Shunji, Kawai Keiichi, Nishii Ryuichi, Jinnouchi Seishi, Ogawara Ken ichi, Higaki Kazutaka, Tamura Shozo, Arimori Kazuhiko, Kimura Toshikiro

机构信息

Department of Hospital Pharmacy, Miyazaki Medical College, Miyazaki 889-1692, Japan.

出版信息

Int J Pharm. 2002 Feb 21;233(1-2):179-90. doi: 10.1016/s0378-5173(01)00942-5.

Abstract

The plasma concentration-time profile of theophylline after oral administration in human volunteers was predicted using the individual gastrointestinal (GI) transit data monitored by a gamma scintigraphic technique. Theophylline was administered as aminophylline under fasted and fed condition, along with 99mTc-labeled diethylenetriamine-pentaacetic acid (DTPA), an unabsorbable marker to evaluate the GI transit by a gamma scintigraphic technique. Two healthy male volunteers participated under fasted and fed conditions in a crossover study. The GI transit was evaluated by dividing the GI tract to four segments, stomach, jejunum, ileum and cecum/colon. Under the fed condition, the GI transit pattern for each segment was confirmed to alter considerably, causing a delay in the gastric emptying mainly. Further, the plasma concentration curves of theophylline after oral administration were predicted using the GI-Transit-Absorption Model on the basis of individual GI transit parameters calculated by the fitting of the observed data to the GI-Transit Kinetic Model. The absorption rate constant in each segment and the pharmacokinetic parameters after intravenous administration used for the prediction were the values extrapolated from the data in rats and the ones normalized from the values in literatures, respectively. The plasma concentration-time curves for theophylline were well predicted using obtained individual GI transit parameters. The analysis using this method could estimate the variable absorption behavior governed by the GI transit in detail.

摘要

利用γ闪烁扫描技术监测的个体胃肠道(GI)转运数据,预测了人类志愿者口服茶碱后的血浆浓度-时间曲线。在禁食和进食条件下,将茶碱作为氨茶碱给药,同时给予99mTc标记的二乙三胺五乙酸(DTPA),一种不可吸收的标记物,通过γ闪烁扫描技术评估胃肠道转运。两名健康男性志愿者在禁食和进食条件下参与了一项交叉研究。通过将胃肠道分为胃、空肠、回肠和盲肠/结肠四个部分来评估胃肠道转运。在进食条件下,每个部分的胃肠道转运模式被证实有显著改变,主要导致胃排空延迟。此外,基于通过将观察数据拟合到胃肠道转运动力学模型计算出的个体胃肠道转运参数,使用胃肠道转运-吸收模型预测了口服茶碱后的血浆浓度曲线。用于预测的各部分吸收速率常数和静脉给药后的药代动力学参数分别是从大鼠数据外推得到的值和从文献值归一化得到的值。利用获得的个体胃肠道转运参数,很好地预测了茶碱的血浆浓度-时间曲线。使用该方法进行分析可以详细估计由胃肠道转运控制的可变吸收行为。

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