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Hydrodynamic, mass transfer, and dissolution effects induced by tablet location during dissolution testing.
J Pharm Sci. 2009 Apr; 98(4):1511-31.JP

Abstract

Tablets undergoing dissolution in the USP Dissolution Testing Apparatus II are often found at locations on the vessel bottom that are off-center with respect to the dissolution vessel and impeller. A previously validated CFD approach and a novel experimental method were used here to examine the effect of tablet location on strain rates and dissolution rates. Dissolution tests were conducted with non-disintegrating tablets (salicylic acid) and disintegrating tablets (Prednisone) immobilized at different locations along the vessel bottom. CFD was used to predict the velocity profiles and strain rates when the tablets were placed at such locations. A CFD-based model was derived to predict the mass transfer coefficient and dissolution curves, which were then compared to the experimental results. Both non-disintegrating and disintegrating off-center tablets experimentally produced higher dissolution rates than centered tablets. The CFD-predicted strain rate distribution along the bottom was highly not uniform and the predicted strain rates correlated well with the experimental mass transfer coefficients. The proposed CFD-based model predicts mass transfer rates that correlate well with the experimental ones. The exact tablet location has a significant impact on the dissolution profile. The proposed model can satisfactorily predict the mass transfer coefficients and dissolution profiles for non-disintegrating tablets.

Authors+Show Affiliations

Otto H. York Department of Chemical, Biological and Pharmaceutical Engineering, New Jersey Institute of Technology, 323 M. L. King Boulevard, Newark, New Jersey 07102-1982, USA.No affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

18781589

Citation

Bai, Ge, and Piero M. Armenante. "Hydrodynamic, Mass Transfer, and Dissolution Effects Induced By Tablet Location During Dissolution Testing." Journal of Pharmaceutical Sciences, vol. 98, no. 4, 2009, pp. 1511-31.
Bai G, Armenante PM. Hydrodynamic, mass transfer, and dissolution effects induced by tablet location during dissolution testing. J Pharm Sci. 2009;98(4):1511-31.
Bai, G., & Armenante, P. M. (2009). Hydrodynamic, mass transfer, and dissolution effects induced by tablet location during dissolution testing. Journal of Pharmaceutical Sciences, 98(4), 1511-31. https://doi.org/10.1002/jps.21512
Bai G, Armenante PM. Hydrodynamic, Mass Transfer, and Dissolution Effects Induced By Tablet Location During Dissolution Testing. J Pharm Sci. 2009;98(4):1511-31. PubMed PMID: 18781589.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hydrodynamic, mass transfer, and dissolution effects induced by tablet location during dissolution testing. AU - Bai,Ge, AU - Armenante,Piero M, PY - 2008/9/11/pubmed PY - 2009/8/6/medline PY - 2008/9/11/entrez SP - 1511 EP - 31 JF - Journal of pharmaceutical sciences JO - J Pharm Sci VL - 98 IS - 4 N2 - Tablets undergoing dissolution in the USP Dissolution Testing Apparatus II are often found at locations on the vessel bottom that are off-center with respect to the dissolution vessel and impeller. A previously validated CFD approach and a novel experimental method were used here to examine the effect of tablet location on strain rates and dissolution rates. Dissolution tests were conducted with non-disintegrating tablets (salicylic acid) and disintegrating tablets (Prednisone) immobilized at different locations along the vessel bottom. CFD was used to predict the velocity profiles and strain rates when the tablets were placed at such locations. A CFD-based model was derived to predict the mass transfer coefficient and dissolution curves, which were then compared to the experimental results. Both non-disintegrating and disintegrating off-center tablets experimentally produced higher dissolution rates than centered tablets. The CFD-predicted strain rate distribution along the bottom was highly not uniform and the predicted strain rates correlated well with the experimental mass transfer coefficients. The proposed CFD-based model predicts mass transfer rates that correlate well with the experimental ones. The exact tablet location has a significant impact on the dissolution profile. The proposed model can satisfactorily predict the mass transfer coefficients and dissolution profiles for non-disintegrating tablets. SN - 1520-6017 UR - https://www.unboundmedicine.com/medline/citation/18781589/Hydrodynamic_mass_transfer_and_dissolution_effects_induced_by_tablet_location_during_dissolution_testing_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0022-3549(16)32938-0 DB - PRIME DP - Unbound Medicine ER -