Current address: Department of Pharmaceutical Sciences, University at Buffalo, State University of New York, Amherst, NY 14260, USA.
Novel gastroretentive controlled-release drug delivery system for amoxicillin therapy in veterinary medicine
Article first published online: 28 DEC 2010
DOI: 10.1111/j.1365-2885.2010.01255.x
© 2010 Blackwell Publishing Ltd
Issue

Journal of Veterinary Pharmacology and Therapeutics
Volume 34, Issue 5, pages 487–493, October 2011
Additional Information
How to Cite
HORWITZ, E., KAGAN, L., CHAMISHA, Y., GATI, I., HOFFMAN, A., FRIEDMAN, M. and LAVY, E. (2011), Novel gastroretentive controlled-release drug delivery system for amoxicillin therapy in veterinary medicine. Journal of Veterinary Pharmacology and Therapeutics, 34: 487–493. doi: 10.1111/j.1365-2885.2010.01255.x
Publication History
- Issue published online: 11 SEP 2011
- Article first published online: 28 DEC 2010
- (Paper received 14 April 2010; accepted for publication 31 October 2010)
- Abstract
- Article
- References
- Cited By
Horwitz, E., Kagan, L., Chamisha, Y., Gati, I., Hoffman, A., Friedman, M., Lavy, E. Novel gastroretentive controlled-release drug delivery system for amoxicillin therapy in veterinary medicine. J. vet. Pharmacol. Therap.34, 487–493.
Beta-lactam antimicrobials, commonly used in both veterinary and human medicine, generally present short biologic half-lives, whereas their activity is enhanced as pathogen exposure is prolonged. These properties necessitate multiple-dose regimens of standard dosage forms, thereby hampering pet owner adherence, frequently resulting in therapeutic failure. This study presents a novel controlled-release gastroretentive oral drug delivery system for beta-lactams with which single-dose administration provides an effective antimicrobial course, optimizing pharmacokinetic (PK)–pharmacodynamic (PD) profiles, minimizing adverse effects and emergence of antimicrobial resistance and facilitating adherence. Our prototype sustained-delivery swelling-tablet (SDST), based on a degradable hydrophilic polymeric matrix, was designed to enable continuous input of these drugs to their absorption sites over several days. Several SDST formulations of the beta-lactam amoxicillin were evaluated in in vitro dissolution studies. Two formulations were selected for further in vivo canine studies, for determination of gastric retention and PK–PD profiling. Prolonged gastric retention times maintaining allowed for maintained effective drug concentrations against many clinically relevant pathogens for more than 48 h for one formulation and more than 5 days for the other. Both SDST formulations offer significant advantages over standard immediate-release therapy in achieving PK–PD goals and enhancing adherence. The prototypical formulations represent a novel platform which may be modified to meet various clinical requirements.

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