PURPOSE: To test the hypothesis that the onset of drug release in vivo from a unique colon-specific drug delivery system (CODES) would depend on the colonic availability rate of lactulose. The site specificity of drug release in canine GI tract was also estimated. METHODS: CODES tablets were prepared by tableting the granulation or acetaminophen and lactulose, followed with film coating. The pharmacokinetic performance of different CODES formulations was evaluated in six beagle dogs under fasted conditions. The release of acetaminophen and lactulose was also characterized in vitro. RESULTS: The onset of acetaminophen release in beagle dogs was found to be dependent on the coating level of Eudragit E and lactulose loading in the core tablet. At Eudragit E coating levels of 4%, 8% and 12% (coating weight gain), the onset of in vivo drug release occurred 5.5 (+/- 1.9) h. 4.8 (+/-1.0) h. and 7.5 (+/-1.0) h, respectively, after dosing. A similar trend was observed when the loading of lactulose in the core tablet decreased from 78% to 58% and 38%. However, the rate and extent of acetaminophen absorption did not vary significantly in each situation based on the values of AUC and Cmax. CONCLUSION: The onset of drug release in vivo from CODES tablets is predominantly dependent on colonic availability rate of lactulose because drug release from this system is triggered by localized drop of colonic pH from the fermentation of lactulose.
PURPOSE: To test the hypothesis that the onset of drug release in vivo from a unique colon-specific drug delivery system (CODES) would depend on the colonic availability rate of lactulose. The site specificity of drug release in canine GI tract was also estimated. METHODS: CODES tablets were prepared by tableting the granulation or acetaminophen and lactulose, followed with film coating. The pharmacokinetic performance of different CODES formulations was evaluated in six beagle dogs under fasted conditions. The release of acetaminophen and lactulose was also characterized in vitro. RESULTS: The onset of acetaminophen release in beagle dogs was found to be dependent on the coating level of Eudragit E and lactulose loading in the core tablet. At Eudragit E coating levels of 4%, 8% and 12% (coating weight gain), the onset of in vivo drug release occurred 5.5 (+/- 1.9) h. 4.8 (+/-1.0) h. and 7.5 (+/-1.0) h, respectively, after dosing. A similar trend was observed when the loading of lactulose in the core tablet decreased from 78% to 58% and 38%. However, the rate and extent of acetaminophen absorption did not vary significantly in each situation based on the values of AUC and Cmax. CONCLUSION: The onset of drug release in vivo from CODES tablets is predominantly dependent on colonic availability rate of lactulose because drug release from this system is triggered by localized drop of colonic pH from the fermentation of lactulose.
Authors: M Uribe; O Campollo; F Vargas; G P Ravelli; F Mundo; L Zapata; S Gil; G Garcia-Ramos Journal: Hepatology Date: 1987 Jul-Aug Impact factor: 17.425
Authors: Min Soo Kim; Dong Woo Yeom; Sung Rae Kim; Ho Yub Yoon; Chang Hyun Kim; Ho Yong Son; Jin Han Kim; Sangkil Lee; Young Wook Choi Journal: Drug Des Devel Ther Date: 2016-12-21 Impact factor: 4.162
Authors: Esther T L Lau; Stuart K Johnson; Barbara A Williams; Deirdre Mikkelsen; Elizabeth McCourt; Roger A Stanley; Ram Mereddy; Peter J Halley; Kathryn J Steadman Journal: Pharmaceutics Date: 2017-05-19 Impact factor: 6.321