Main Article Content
Cefadroxil is a broad spectrum antibiotic that acts against an extensive variety of bacteria, including Gram-positive and Gram-negative bacteria. The major drawback of orally administered drug like cefadroxil is its shorter half life of 1.2 hrs. The goal of the study is to prolong the drug release, producing a desired blood serum level, reduction in drug toxicity and improving the patient compliance by prolonging the dosing intervals. The present research highlights the formulation and evaluation of cefadroxil loaded microbeads using polymers such as carbopol and sodium carboxy methyl cellulose while sodium alginate being the common polymer with a cross linking agent being calcium chloride. The beads were prepared by “Ionotropic gelation technique” and characterized for its particle size shape, micromeritic properties, percentage drug loading, percentage drug entrapment efficiency, swelling ratio and In vitro drug release studies. The release studies were obtained up to 12 hrs from 3 batches. The in vitro release data were fit to different equations and kinetic models to explain release profiles. The kinetic models used were zero order, Higuchi’s and Peppa’s. The correlation coefficient value (r) indicates the kinetic of drug release was zero order and the mechanism of drug release was found to be super case II transport.
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.