In vitro dissolution and in vivo bioequivalence evaluation of two brands of trimetazidine tablets
Author:
Affiliation:
1. Department of Pharmaceutics; Faculty of Pharmacy; Damanhour University; Damanhour Egypt
2. Bioavailability Unit; Faculty of Pharmacy; Tanta University; Tanta Egypt
Funder
PHARCO Pharmaceuticals, Alexandria, Egypt
Publisher
Wiley
Subject
Pharmacology (medical),Pharmaceutical Science
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cpdd.63/fullpdf
Reference17 articles.
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3. LC/ESI-MS method for the determination of trimetazidine in human plasma: Application to a bioequivalence study on Chinese volunteers;Jiao;J Pharm Biomed Anal.,2007
4. Pharmacokinetic profile of a modified release formulation of trimetazidine (TMZ MR 35 mg) in the elderly and patients with renal failure;Barré;Biopharm Drug Dispos.,2003
5. Food effect on bioavailability of modified release trimetazidine tablets;Ozbay;J Clin Pharmacol.,2012
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2. The effect of trimethazidine on mortality in an experimental acute pancreatitis model1;The Turkish Journal of Gastroenterology;2020-09-07
3. Validated RP-HPLC method for quantification of doxazosin in human plasma: Application in a bioequivalence study;Annales Pharmaceutiques Françaises;2020-01
4. Overcoming interference of plasma phospholipids using HybridSPE for the determination of trimetazidine by UPLC-MS/MS;Biomedical Chromatography;2017-10-02
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