Characterization of Human Duodenal Fluids in Fasted and Fed State Conditions

被引:167
|
作者
Riethorst, Danny [1 ]
Mols, Raf [1 ]
Duchateau, Guus [2 ]
Tack, Jan [3 ]
Brouwers, Joachim [1 ]
Augustijns, Patrick [1 ]
机构
[1] Katholieke Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Drug Delivery & Disposit, Leuven, Belgium
[2] Unilever R&D, Nutr & Hlth, Vlaardingen, Netherlands
[3] Univ Hosp Leuven, Dept Gastroenterol, Leuven, Belgium
关键词
intestinal drug absorption; intestinal secretion; gastrointestinal; oral drug delivery; food effects; lipids; pH; phospholipids; WATER-SOLUBLE DRUGS; MIXED MICELLES; IN-VITRO; ABSORPTION; SOLUBILIZATION; PHOSPHOLIPIDS; CHOLESTEROL; DISSOLUTION; PREDICTION; LIPOLYSIS;
D O I
10.1002/jps.24603
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This work provides an elaborate characterization of human intestinal fluids (HIF) collected in fasted-and fed-state conditions. HIF from 20 healthy volunteers (10 M/F) were aspirated by intubation near the ligament of Treitz in a time-dependent manner (10-min intervals) and characterized for pH, bile salts, phospholipids, cholesterol, triacylglycerides (TAG), diacylglycerides (DAG), monoacylglycerides (MAG), free fatty acids (FFA), pancreatic lipase, phospholipase A2, and nonspecific esterase activity. For almost all parameters, a food-induced effect was observed. Results were characterized by a high variability, as illustrated by the broad ranges observed for each parameter: pH (fasted: 3.4-8.3; fed: 4.7-7.1), bile salts (fasted: 0.03-36.18 mM; fed: 0.74-86.14 mM), phospholipids (fasted: 0.01-6.33 mM; fed: 0.16-14.39 mM), cholesterol (fasted: 0-0.48 mM; fed: 0-3.29 mM), TAG (fed: 0-6.76 mg/mL), DAG (fed: 0-3.64 mg/mL), MAG (fasted: 0-1.09 mg/mL; fed: 0-11.36 mg/mL), FFA (fasted: 0-3.86 mg/mL; fed: 0.53-15.0 mg/mL), pancreatic lipase (fasted: 26-86 g/mL; fed: 146-415 g/mL), phospholipase A2 (fasted: 3-6 ng/mL; fed: 4.3-27.7 ng/mL), and nonspecific esterase activity (fasted: 270-4900 U/mL; fed: 430-4655 U/mL). This comprehensive overview may serve as reference data for physiologically based pharmacokinetic modeling and the optimization of biorelevant simulated intestinal fluids for the use in in vitro dissolution, solubility, and permeability profiling. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:673 / 681
页数:9
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