Oral ileocolonic drug delivery by the colopulse-system: A bioavailability study in healthy volunteers

被引:28
|
作者
Schellekens, R. C. A. [1 ,2 ]
Stellaard, F. [3 ]
Olsder, G. G. [1 ]
Woerdenbag, H. J. [2 ]
Frijlink, H. W. [2 ]
Kosterink, J. G. W. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Hosp & Clin Pharm, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Dept Pharmaceut Technol & Biopharm, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Lab Med, NL-9700 RB Groningen, Netherlands
关键词
Colon delivery; ColoPulse; Stable isotope; Intestinal metabolism; Bioavailability; Urea;
D O I
10.1016/j.jconrel.2010.05.028
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The release profile of a novel oral ileocolonic drug delivery technology (ColoPulse-technology) was assessed by a combination of conventional kinetics of a marker substance in blood and site-specific signaling by stable isotope technology. Since ileocolonic delivery involves the drug release in a region in which bacteria are highly present, a prolonged lag time should coincide with proven bacterial enzyme activity. The latter can be tested using C-13-urea as the marker substance. The study was designed as a two period (uncoated versus coated capsule) crossover single dose bioavailability study in healthy subjects. The C-13-recovery data after oral administration of C-13-urea using the ColoPulse delivery system showed a delayed sigmoid release in all subjects with a lag time of >3 h (median: 330 min.). Release was achieved in a urease-containing intestinal segment in all healthy subjects. Complete release in the ileocolonic region was achieved in 10 of 11 subjects. The ColoPulse-technology therefore enables specific and reliable drug delivery in the ileocolonic region in healthy volunteers. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:334 / 340
页数:7
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