Low molecular weight heparin (LMWH) is an agent of choice in the anticoagulant therapy and prophylaxis of thrombosis and coronary syndromes. However, the therapeutic use is partially limited due to a poor oral bioavailability. It was therefore the aim of this study to design and evaluate a highly ef
Scintigraphic evaluation of a novel colon-targeted delivery system (CODES™) in healthy volunteers
✍ Scribed by Masataka Katsuma; Shunsuke Watanabe; Shigeo Takemura; Kazuhiro Sako; Toyohiro Sawada; Yoshinori Masuda; Katsutoshi Nakamura; Muneo Fukui; Alyson L. Connor; Ian R. Wilding
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 448 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
✦ Synopsis
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 AE 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.
📜 SIMILAR VOLUMES
The aim of this study was to estimate colon-specific drug delivery of a novel capsule (CS capsule). Theophylline was used as model drug and little was released from the CS capsules in the release medium mimicking physiological environment of stomach to small intestine. However, 66.7 +/- 8.8% theophy