Gastrointestinal transit of model mini-tablet controlled release oral dosage forms in fasted human volunteers
- PMID: 17637188
- DOI: 10.1211/jpp.59.7.0005
Gastrointestinal transit of model mini-tablet controlled release oral dosage forms in fasted human volunteers
Abstract
The aim of this study was to compare the gastrointestinal transit of multiple unit, small diameter (3.2 mm), non-disintegrating tablets of differing densities with results previously reported in the same volunteers in the fasted state for larger diameter (6.6 and 12.2 mm) tablets. The gastrointestinal transit was observed with gamma-scintigraphy at various intervals over a 9-h period to give an accurate assessment of the transit characteristics. The value for the median emptying time of the first light tablet was significantly shorter than that for the dense tablet, but the total emptying time and the time for the last tablet to empty for both sets of tablets were not statistically different. The value of the median time for initial and final emptying of the small tablets from the stomach was significantly longer than that for the larger diameter tablets. The 9-h time limit of the observations limited the estimation of the time taken to enter the caecum and consequently the small intestine transit times. There was clear evidence that for the dense tablets of all sizes, the value for the small intestine transit time was longer than the 3-4 h reported in the literature. The only tablet system to enter the caecum within the time limit of the study was the normal density 12.2-mm tablets.
Similar articles
-
The influence of non-disintegrating tablet dimensions and density on their gastric emptying in fasted volunteers.J Pharm Pharmacol. 2007 Jan;59(1):23-7. doi: 10.1211/jpp.59.1.0004. J Pharm Pharmacol. 2007. PMID: 17227617 Clinical Trial.
-
Meal-induced acceleration of tablet transit through the human small intestine.Pharm Res. 2009 Feb;26(2):356-60. doi: 10.1007/s11095-008-9749-2. Epub 2008 Nov 4. Pharm Res. 2009. PMID: 18982248 Clinical Trial.
-
Analysis of small intestinal transit and colon arrival times of non-disintegrating tablets administered in the fasted state.Eur J Pharm Sci. 2015 Jul 30;75:131-41. doi: 10.1016/j.ejps.2015.03.001. Epub 2015 Mar 11. Eur J Pharm Sci. 2015. PMID: 25769525
-
Gastroretentive dosage forms.Crit Rev Ther Drug Carrier Syst. 1993;10(2):143-95. Crit Rev Ther Drug Carrier Syst. 1993. PMID: 8370085 Review.
-
Gastric retentive dosage forms: a review.Crit Rev Ther Drug Carrier Syst. 2003;20(6):459-97. doi: 10.1615/critrevtherdrugcarriersyst.v20.i6.30. Crit Rev Ther Drug Carrier Syst. 2003. PMID: 14979868 Review.
Cited by
-
Achieving antral grinding forces in biorelevant in vitro models: comparing the USP dissolution apparatus II and the dynamic gastric model with human in vivo data.AAPS PharmSciTech. 2011 Jun;12(2):620-6. doi: 10.1208/s12249-011-9616-z. Epub 2011 May 10. AAPS PharmSciTech. 2011. PMID: 21557037 Free PMC article. No abstract available.
-
Gastric emptying of pellets under fasting conditions: a mathematical model.Pharm Res. 2009 Jul;26(7):1607-17. doi: 10.1007/s11095-009-9869-3. Epub 2009 Apr 1. Pharm Res. 2009. PMID: 19337822
-
The transit of oral premedication beyond the stomach in patients undergoing laparoscopic sleeve gastrectomy: a retrospective observational multicentre study.BMC Surg. 2023 Nov 4;23(1):335. doi: 10.1186/s12893-023-02246-6. BMC Surg. 2023. PMID: 37924061 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources