Controlled release matrix tablets of glipizide: Influence of different grades of ethocel and Co-excipient on drug release

Journal Title: Pakistan Journal of Pharmaceutical Sciences - Year 2016, Vol 29, Issue 3

Abstract

 The aim of the current study was to formulate and evaluate glipizide controlled release matrix tablets by means of different grades of polymer Ethoceland different co-excipients in order to evaluate their effect on drug release profiles during in vitro dissolution studies. Type II diabetes mellitus is usually treated with Glipizide. Glipizide belongs to sulfonylurea group. Gastric disturbance and severe hypoglycemia has been observed after taking glipizide orally. To overcome these problems, controlled release matrices were developed using different grades of ethyl cellulose polymer with a drug-polymer ratio of 1:3by the direct compression method. The effect on drug release of partial replacement of lactose by different co-excipients, HPMC K100M, starch and CMC, were also studied. Diameter, thickness, hardness, friability, weight variations, drug contents of formulations were tested, these properties were within prescribed limits. Co-excipients and polymer containing formulations were compared to the without co-excipients and polymer containing formulations with respect to their release profile. After a 24-hour release study, ethyl cellulose polymer containing formulation exhibited prolonged release for 5-16 hours; however the polymer Ethocel® standard FP 7 Premium without co-excipient containing formulation exhibited controlled release for 24 hours. Incompatibility was investigated between drugs, co-excipient DSC and polymer study was performed and any type of interaction was not found. Different kinetic models were used to study the release mechanism. An enhanced release rate was observed in case of excipients containing formulations.

Authors and Affiliations

Saif Ullah Mehsud , Gul Majid Khan , Abid Hussain , Muhammad Akram , Muhammad Akhlaq , Kamran Ahmad Khan , Abdul Shakoor

Keywords

Related Articles

 Clinical evaluation of herbal coded formulation Cran-off to Urixin in the treatment of Urinary tract infection

 Urinary Tract Infections are the largest group of infections after the respiratory tract infections. In 85% of the cases the causative organism is E. Coli. A clinical trial was conducted to evaluate the efficacy of...

 Comparative Pharmacognostic evaluation of some species of the genera Suaeda and Salsola leaf (Chenopodiaceae)

 The genera Suaeda and Salsola are halophytic plants belong to the family Chenopodiaceae. Species of these genera have been extensively used in traditional medicines against many diseases due to their various bioact...

 Synthesis, characterization and biological evaluation of some 5-methylpyrazine carbohydrazide based hydrazones

 Pyrazine carbohydrazide based hydrazones were synthesized starting from 5-methylpyrazine-2-carboxylic acid. The acid was first converted to its methyl ester, which on further treatment with hydrazine hydrate transf...

 Preparation and characterization of two new forced degradation products of letrozole and development of a stability-indicating RP-LC method for its determination

 Two new hydrolytic products of letrozole were identified and proved to be true degradation products obtained by alkaline and acidic degradation of the drug. The acid and amide forms of the nitrile groups of letrozo...

 In vitro screening of mucus and solvent extracts of Eisenia foetida against human bacterial and fungal pathogens

 Earthworms are macro invertebrate and have been widely used as therapeutic drugs for thousands of years. In the current research, experiments viz., the antibacterial, antifungal and antioxidant activity of mucus an...

Download PDF file
  • EP ID EP90817
  • DOI -
  • Views 88
  • Downloads 0

How To Cite

Saif Ullah Mehsud, Gul Majid Khan, Abid Hussain, Muhammad Akram, Muhammad Akhlaq, Kamran Ahmad Khan, Abdul Shakoor (2016).  Controlled release matrix tablets of glipizide: Influence of different grades of ethocel and Co-excipient on drug release. Pakistan Journal of Pharmaceutical Sciences, 29(3), 779-787. https://europub.co.uk/articles/-A-90817