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Prin. K. M. Kundnani College of Pharmacy established Department of Pharmaceutical Analysis for the first time in India in 1992, realizing the importance of the subject to the Pharmaceutical and Allied Industry. The permission for the same was granted by AICTE in 1995 which was subsequently ratified by University of Mumbai.

The research laboratory for Pharmaceutical Analysis is the central part of all the departments. It is equipped with latest analytical state-of-the-art equipments and trained analyst to undertake pharmaceutical analysis. The analytical method development and its validation of new drug substance, new drug products is our main area of interest. Analysis of biological fluids and herbal formulations is also carried out. The major research programmes are largely focused on stability indicating assay method development. All the research data generated comply with regulatory requirements. There are two recognized M. Pharm. guide and one recognized Ph.D. guides in the department.

Faculty members(Currently guiding post graduate students):
Dr. (Mrs.) Purnima D. Hamrapukar : HOD and Professor
Mr. Pradeep N. Agarwal : Associate Professor

Grant sanctioned : Rs. 25, 45, 470/-

Funding agencies : AICTE, University of Mumbai, Industry Projects

Areas of Interest :
1. Analytical studies of drugs and related substances
2. Analytical method development and validations
3. Trace and Ultra-trace level impurity detection
4. Studies on Stability indicating assays
5. Analytical studies of herbals using sophisticated instrumentation
6. We have developed new analytical assay techniques for drugs like Tadalafil, Valdagliptin, Ziprasidone, Datclatsvir, Dolutagravir and others

Number of Publications : 19

Important Publications in last five years:
1. HPLC Method for the Determination of Emtricitabine and Related Degradation Substances,Journal of chromatographic sciences., Vol. 51, Pg 419-424, 2013.
2. Optimizaton and Validation of RP-HPLC Stability Indicating Method for Determination of Olmesartan Medoxomil and its Degraded Product, International Journal of Applied Science and Engineering.,Vol. 11(2), 137-147, 2013.
3. Study of Doxyfylline and its Degradation Products in Bulk Drug by a Newly Developed Stability-Indicating HPLC Method, Journal of AOAC International., Vol. 96(4),765-770, 2013.
4. Development and Validation of Stability Indicating RP-HPLC Method for Troxipide from Bulk Drug. International Journal of Research in Pharmaceutical and Biomedical Sciences., Vol. 4(4), 1179-1186, 2013.
5. Development and Validation of Stability Indicating RP-HPLC Method for estimation of Locosamide in bulk and its pharmaceutical formulation. International Journal of Pharmaceutical Science., Vol. 28(2),164-168, 2014. Number of Presentations at Scientific Conferences: 09(In last three years)

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