Scintigraphic evaluation of a novel colon-targeted delivery system (CODES™) in healthy volunteers

被引:49
作者
Katsuma, M
Watanabe, S
Takemura, S
Sako, K
Sawada, T
Masuda, Y
Nakamura, K
Fukui, M
Connor, AL
Wilding, IR
机构
[1] Yamanouchi Pharmaceut Co Ltd, Nova Pharmaceut Labs, DDS Res, Yaizu, Shizuoka 4250072, Japan
[2] Yamanouchi Pharmaceut Co Ltd, Nova Pharmaceut Labs, Parenteral Formulat Res, Shizuoka 4250072, Japan
[3] Yamanouchi Pharmaceut Co Ltd, Nova Pharmaceut Labs, Shizuoka 4250072, Japan
[4] Pharmaceut Profiles Ltd, Nottingham NG11 6JS, England
关键词
colonic drug delivery; lactulose; gastrointestinal transit; scintigraphy; disintegration profile; food effects; human;
D O I
10.1002/jps.20063
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The purposes of this study are to investigate the gastrointestinal transit and release properties of a novel, colon-targeted delivery system (CODES(TM)) administered to healthy volunteers using gamma scintigraphy and to confirm that lactulose functions to promote disintegration in the colon. Two placebo formulations were studied: one was CODES(TM), which consisted of a lactulose containing core overcoated with both Eudragit E and Eudragit L designed to rapidly disintegrate in the colon, the other was lactulose-free reference formulation (LFRF) that consisted of lactulose-free tablet core overcoated with the same materials. Transit and disintegration of the radiolabeled formulations were followed by gamma scintigraphy. In the fasted state, scintigraphic images indicated that CODES(TM) started to disintegrate in the ascending colon in the majority of subjects at 7.11 +/- 2.01 h post-dose. Disintegration was complete within 1 h following commencement of in vivo release. In contrast, LFRF presented with prolonged in vivo disintegration properties. In the fed state, the disintegration period of CODES(TM) was almost comparable to that observed in the fasted state. Gamma scintigraphic studies clearly showed that CODES(TM) provides for rapid target site release in the colon regardless of the ingestion of food. (C) 2004 Wiley-Liss, Inc. and the American Pharmacists. Association.
引用
收藏
页码:1287 / 1299
页数:13
相关论文
共 23 条
[1]   The use of scintigraphy to provide ''proof of concept'' for novel polysaccharide preparations designed for colonic drug delivery [J].
Adkin, DA ;
Kenyon, CJ ;
Lerner, EI ;
Landau, I ;
Strauss, E ;
Caron, D ;
Penhasi, A ;
Rubinstein, A ;
Wilding, IR .
PHARMACEUTICAL RESEARCH, 1997, 14 (01) :103-107
[2]   COLONIC TRANSIT OF DIFFERENT SIZED TABLETS IN HEALTHY-SUBJECTS [J].
ADKIN, DA ;
DAVIS, SS ;
SPARROW, RA ;
WILDING, IR .
JOURNAL OF CONTROLLED RELEASE, 1993, 23 (02) :147-156
[3]   VARIATION IN GASTROINTESTINAL TRANSIT OF PHARMACEUTICAL DOSAGE FORMS IN HEALTHY-SUBJECTS [J].
COUPE, AJ ;
DAVIS, SS ;
WILDING, IR .
PHARMACEUTICAL RESEARCH, 1991, 8 (03) :360-364
[4]   A COMPARATIVE-STUDY OF THE GASTROINTESTINAL TRANSIT OF A PELLET AND TABLET FORMULATION [J].
DAVIS, SS ;
HARDY, JG ;
TAYLOR, MJ ;
WHALLEY, DR ;
WILSON, CG .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1984, 21 (02) :167-177
[5]   TRANSIT OF PHARMACEUTICAL DOSAGE FORMS THROUGH THE SMALL-INTESTINE [J].
DAVIS, SS ;
HARDY, JG ;
FARA, JW .
GUT, 1986, 27 (08) :886-892
[6]  
FUJINO S, 1995, RINSHOIYAKU, V11, P1357
[7]   Preparation of enteric coated timed-release press-coated tablets and evaluation of their function by in vitro and in vivo tests for colon targeting [J].
Fukui, E ;
Miyamura, N ;
Uemura, K ;
Kobayashi, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 204 (1-2) :7-15
[8]   ORAL DELAYED-RELEASE SYSTEM FOR COLONIC SPECIFIC DELIVERY [J].
GAZZANIGA, A ;
IAMARTINO, P ;
MAFFIONE, G ;
SANGALLI, ME .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 108 (01) :77-83
[9]   GASTRIC-EMPTYING OF SOLIDS IN MAN [J].
HOLT, S ;
REID, J ;
TAYLOR, TV ;
TOTHILL, P ;
HEADING, RC .
GUT, 1982, 23 (04) :292-296
[10]   VOLUME AND ENERGY CONTENT OF MEALS AS DETERMINANTS OF GASTRIC-EMPTYING [J].
HUNT, JN ;
STUBBS, DF .
JOURNAL OF PHYSIOLOGY-LONDON, 1975, 245 (01) :209-225