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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>11</Volume><Issue>1</Issue></Journal><ArticleTitle>Pharmacokinetics and Comparative Bioavailability of Two Diltiazem Tablet Formulations in Healthy Volunteers</ArticleTitle><FirstPage>14</FirstPage><LastPage>8</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Simin Dadashzadeh</LastName></Author><Author><FirstName></FirstName><LastName>Afshin Zarghi</LastName></Author><Author><FirstName></FirstName><LastName>A. J. Ebrahimian</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>The pharmacokinetic parameters and bioavailability of diltiazem following a single oral administration of a generic diltiazem 60 mg tablet (Sobhan Pharmaceuticals, Iran) were compared to those of a reference product (Entrydil, Orion Pharmaceuticals, Finland). Twelve healthy male volunteers received a single oral dose of either formulation following overnight fasting in a double blind, randomized, crossover study. Blood samples were collected at selected times during 24 h and diltiazem plasma concentrations were determined with a sensitive HPLC method. Individual pharmacokinetic parameters, t1/2, t1/2(abs), K, Ka, Tmax, Cmax, Vd/F, Cl/F, AUC0-24 and AUC0-&amp;#8734; were calculated. No significant differences were observed in pharmacokinetic parameters between two formulations. The 90% confidence intervals for the test/reference geometric mean ratios of Cmax, AUC0-24 AUC0-&amp;#8734; and Cmax/AUC0-&amp;#8734;  were within the conventional  bioequivalence range of 0.8 - 1.25. 

 In-vitro parameters of mean dissolution time (MDT) and time for 70 % dissolution (T70)  were also determined. There was a significant difference between the MDT for two dosage forms (p</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/161</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/161/161</pdf_url></Article></Articles>
