Login

Journal Front Page

News & Events

  • April 2024 Issue delayed
  • Dear Researcher, It Pleased to inform you that, Asian Journal of Pharmaceutical Education and Research, Volume 13, Issue 2 (April 2024) Issue) schedule published on 15 April 2024 is delay due to some technical problem. It will published on 22 April 2024. Sorry for inconvenience. For other details You can vist the website http://www.ajper.com
  • Call for article for April 2024 issue
  • Submissions of Review, Research Article, Short Communication and Case study are being accepted for the current and future issues before 15 March, 2024 of this journal by online process or editor@ajper.com, or ajper.editor@gmail.com. Further information can be found at www.ajper.com.
  • January 2024 Issue published
  • Dear Researcher, It Pleased to inform you that, Asian Journal of Pharmaceutical Education and Research, has successfully launch Volume 13, Issue 1 (January 2024) Issue). You can find the article on http://ajper.com/current_issue.php Article also invited for the Next coming Issue from your side. For More details Visit: www.ajper.com
  • Application For Reviewer
  • We are now going to reconstitute our editorial board members of Reviewer. Please send your resume at ajper.editor@gmail.com and be a part of the editorial board member as Reviewer.
  • AJPER Impact facor
  • It is to pleasure that Ajper SJIF imact facor has increse from 5.019 to 7.014. Also global impact factor incresed from 0.654 to 0.765.
  • ICV
  • AJPER Rank with Index Copernicus Value 61.10 due to high reputation at International Level

Abstract

Formulation and in-vitro Evaluation of Mefanemic acid Solid Dispersion

Vipul Jain*, Sukhwant Singh, Jitendra Banveer

Sagar Institute of Research Technology and Pharmacy, Bhopal, M.P

ABSTRACT

The objective of the research work to enhance the solubility of mefanemic acid by formulating solid dispersion with hydrophilic polymers such as poly ethylene glycol (PEG 4000) and ethyl cellulose as carrier and solid dispersions were prepared by the method of conventional and physical mixture technique. Further formulated as tablet and capsular dosage forms and were evaluated for drug content, Invitro dissolution studies and differential scanning calorimetry. Results showed that formulations F1-F5 varied from 58.41-96.91% of drug content, release 20-70% of drug in 60 minutes and follows Hixson crowell dissolution release kinetics. DSC Studies shows that there is no evidence of interaction between drug-excipient and as the solid dispersion exhibited no endothermic peak. During the stability study it was found that at low temperature the capsule shell breakdown and does not able to maintain its physical integrity and at high temperature and RH conditions therefore storage preferably below 300C will make stable formulations.

Keywords: Solubility enhancement, poly ethylene glycol, solid dispersions, differential scanning calorimetry, Hixsoncrowell.


[Full Text Article]