| Literature DB >> 15067705 |
Masataka Katsuma1, Shunsuke Watanabe, Shigeo Takemura, Kazuhiro Sako, Toyohiro Sawada, Yoshinori Masuda, Katsutoshi Nakamura, Muneo Fukui, Alyson L Connor, Ian R Wilding.
Abstract
The purposes of this study are to investigate the gastrointestinal transit and release properties of a novel, colon-targeted delivery system (CODES) 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, 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 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 was almost comparable to that observed in the fasted state. Gamma scintigraphic studies clearly showed that CODES provides for rapid target site release in the colon regardless of the ingestion of food. Copyright 2004 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 93:1287-1299, 2004Entities:
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Year: 2004 PMID: 15067705 DOI: 10.1002/jps.20063
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534