Venkateswarlu Kudupudi * } ?>
, Kusuma D } ?>
, } ?>
, } ?>
, } ?>
Status: Published
The aim of present study is to formulate an intravenous injection of Vancomycin Hydrochloride. It was belongs to the category of antibiotic and it was widely used in staphylococcal endocarditis. The main objective of the study was to develop rapid reconstituted formulation of Vancomycin Hydrochloride by using lyophilization technology. The lyophilization was carried in different batches of the Vancomycin Hydrochloride were prepared with varying the excipients and its concentration while keeping the lyophilization cycle constant. An optimized lyophilization cycle of 36 hours was achieved. The optimized lyophilized product was subjected to in vitro parameters such as cake appearance, reconstitution time, PH, assay, RS, particulate matter, water content, IR, color value, % light transmittance, DSC. After considering all product characteristics batch-6 was considered as an optimized formulation.