Dr Krishnamurthy Bhat
Professor & Vice-Principal
Date of Joining: 25.06.2004
Department of Pharmaceutical Quality Assurance
CURRENT ACADEMIC ROLE & RESPONSIBILITIES
Dr. Krishnamurthy Bhat is actively involved in the academic and research activities of the department. He has many funded projects ongoing under his supervision.
Dr. Bhat supervises Mpharm and Ph.D. students, and teaches undergraduates and postgraduates. He also has administrative responsibilities.
SUBJECTS CURRENTLY TEACHING
| Subject | Semester / Year |
|---|---|
| Pharmaceutical Analysis-II | Final year Bharm |
| Pharmaceutical Analysis Lab | Final year Bharm |
| Modern Pharmaceutical Analytical Techniques | MPharm- First semester |
| Documentation and Regulatory Writing | MPharm- First semester |
| Regulatory Affairs practicals-I | MPharm- First semester |
ACADEMIC QUALIFICATIONS
| Degree | Specialisation | Institute | Year of passing |
|---|---|---|---|
| BPharm | JSS College of Pharmacy, Mysore | 1991 | |
| MPharm | Quality Assurance | LM College of Pharmacy | 1995 |
| Ph.D. | Pharmaceutical Sciences | Gujarat University | 2004 |
Experience
| Institution / Organisation | Designation | Role | Tenure |
|---|---|---|---|
| LM College of Pharmacy: Ahmedabad, Gujarat, India | Senior Research Scholar | Researcher | 1.5 years |
| KB Institute of Pharmaceutical Education and Research: Gandhinagar, Gujarat, India | Lecturer | Teaching | 06 years |
| KB Institute of Pharmaceutical Education and Research: Gandhinagar, Gujarat, India | Assistant Professor | Teaching | 05 Months |
| Manipal College of Pharmaceutical Sciences: Manipal, Karnataka, India | Lecturer | Teaching and Research | 01 year |
| Manipal College of Pharmaceutical Sciences: Manipal, Karnataka, India | Associate Professor | Teaching and Research | 03 Years |
AREAS OF INTEREST, EXPERTISE AND RESEARCH
Area of Expertise
Pharmaceutical Analysis, Pharmaceutical Materials Science, Pharmacokinetics
Professional Affiliations & Contributions
Dr. Krishnamurthy Bhat has a primary research interest in analytical method development and validation for new drugs and new methods for existing drugs. This is evidenced by his publication list of various analytical techniques and instrument combinations. He is also an avid follower of drug regulations of important countries and does some research on the evolution of comparison of these regulations. Crystal engineering and formulation modifications as tools for improving bioavailability of drugs are another area where Dr. Bhat is actively researching.
His expertise in these areas can be judged by his publications in journals like Arzneimittel-Forschung, Journal of Pharmaceutical and Biomedical Analysis, European Journal of Pharmaceutical Sciences, European Journal of Pharmaceutics and Biopharmaceutics etc. He is also an reviewer for few journals, expert committee members for various universities across the country.
The author credentials and citation graphs can be accessed by following platforms,
Scopus author ID: 25937181100
ORCID ID: orcid.org/0000-0002-8604-472X
Google scholar link:
http://scholar.google.co.in/citations?view_op=search_authors&mauthors=krishnamurthy+bhat&hl=en&oi=ao
Peer review record can be verified at:
PUBLON ID: publons.com/author/741664/Krishnamurthy-bhat#profile
Work Experience
| Organisation | Role | Tenure |
|---|---|---|
| Bangalore Pharmaceutical and Research Labs Pvt Ltd: Bangalore, Karnataka, India | Manufacturing Executive | 04 Years |
| Bangalore Pharmaceutical and Research Labs Pvt Ltd: Bangalore, Karnataka, India | Quality Assurance Executive | 01 year |
LC determination and pharmacokinetics of meloxicam.
B Dasandi H Saroj Krishnamurthy Bhat
Journal of pharmaceutical and biomedical analysis, Vol. 28 (2002)
Simultaneous determination of pioglitazone and glimepiride in bulk drug and pharmaceutical dosage form by RP-HPLC method
A Karthik G Subramanian CM Rao Krishnamurthy Bhat P Musmade M Surulivel Rajan
Pakistan journal of pharmaceutical sciences, Vol. 21 (2008)
Enhanced oral absorption of saquinavir with methyl-beta-cyclodextrin—preparation and in vitro and in vivo evaluation
SM Pathak P Musmade A Karthik Krishnamurthy Bhat Nayanabhirama Udupa
European Journal of Pharmaceutical Sciences, Vol. 41 (2010)
Estimation of Stavudine, Lamivudine and Nevirapine by Chemometric UV Spectroscopic Method
A Gupta ST Bhagawati Muddukrishna Badamane Sathyanarayana Krishnamurthy Bhat
Ind J Pharm Edu Res, Vol. 46
Preparation and characterization of co-amorphous Ritonavir–Indomethacin systems by solvent evaporation technique: Improved dissolution behavior and physical stability without evidence of intermolecular interactions
OP Ranjan SS Hussen Muddukrishna Badamane Sathyanarayana PB Musmade Krishnamurthy Bhat
European Journal of Pharmaceutical Sciences, Vol. 62, (2013)
Simultaneous estimation of emicitrabine, efavirenz, tenofovir disproxil fumerate by chemometry and reverse phase high performance liquid chromatography.
G. ramya Kumari Deepika N. C. Krishnamurthy Bhat
53(06) June 2016, 62 – 69.
Bioavailability enhancement of Rizatriptan Benzoate by oral disintegrating Strip: In vitro and in vivo evaluation.
S. T. Bhawati Ankita D. Chonkar Krishnamurthy Bhat
Current Drug Delivery 2016 13(3), 462 - 70.
Development and validation of reversedphase highperformance liquid chromatography method for estimation of rizatriptan benzoate in oral strip formulations.
S. T. Bhagawati Kiran Avadani Muddukrishna Badamane Sathyanarayana Krishnamurthy Bhat
J. of Basic and Clinical Pharmacy 6(1) December – February 2015, 7 – 11.
Trademark and their related issues
Ankur Singh
MPharm Part-II (2015)
Clinical research and it’s regulatory impact in India
Smita Sagarika B
MPharm Part-II (2015)
Regulatory Scenrio of Prefilled syringes in developed markets
MD Sadiq Pasha
MPharm Part-II (2015)
Significance of regulatory information management in pharmaceutical industry
Vinay Thallapally
MPharm Part-II (2015)
Development and Validation of an analytical method for related substances in N-Acetyl-L-Cystine Effervescent tablets by RP-HPLC
Elizabeth Marry Mathew
MPharm Part-II (2015)
Qualification and facility validation of sterile dry powder for injections.
Deepika N. C.
MPharm part-II (2016)
Bioanalytical method development and validation for the quantification of sofosbuvir in human plasma by RP – HPLC.
Rahul U. Rathod
MPharm part-II (2016)
Analytical method development and validation for the determination of moxifloxacon in marketed formulations by using HPLC – ECD.
G. Phani Sekhar Reddy
MPharm part-II (2016)