Name: Dr. Nageswara rao Reddy
Educational Qualification: Ph.D.
Designation: Project Manager at Sannova Analytical Inc, New Jersey, USA.
University: Berhampur University
Research Interests: Pharmaceutical Analysis using LC/MS, GC/MS, HPLC, ICP/MS, Nanocapsules, Liposomal, PEG ylated Peptides and Proteins.
Biography: Dr. Nageswara rao Reddy is currently working as Project Manager at Sannova Analytical Inc, New Jersey, USA. He obtained his Ph.D. in Pharmacy from Berhampur University, Orissa, India. Master’s in pharmacy from College of Pharmaceutical Sciences, Berhampur, Orissa, India. He has about 14 years of experience in Bioanalytical and Analytical Research & Development (R&D) for Pharmaceuticals and CRO companies. Validated more than 50 generic molecules and performed sample analysis for more than 100 different biostudies under GLP regulations in which most of studies have been submitted to regulatory agencies like FDA-USA, EMA-Europe, and ANVISA-Brazil. He served as a reviewer for several journals, one of the editorial board members for International Journal of Food Science and Biotechnology (IJFSB) and Editor in chief for International Journal of Pharma and Chemical Research. He has over 15 publications in peer reviewed journals in his credit.
1.UV Spectrophotometric methods for the estimation of Lercanidipine and Isradipine in bulk and Pharmaceutical formulations-Asian Journal of Chemistry, Vol.16 pp l950-1952 (2004).
2.UV Spectrophotometric methods for the determination of Butorphanol Tartrate and Telmisartan in bulk and Pharmaceutical formulations-Asian Journal of Chemistry, Vol.16 pp l953-1955 (2004).
3.A Comparative Study of UV Spectrophotometric method for the Determination of Ethamsylate-Asian Journal of Chemistry, Vol.16 pp l956-1958 (2004).
4.HPLC method for the estimation of Isradipine in the Pharmaceutical dosage forms -International Journal of Chemical Sciences, Vol.2 (3), 2004, 345-350.
5.Development And validation of reverse phase HPLC method for the analysis of Lercanidipine in Pharmaceutical dosage forms-Oriental Journal of Chemsitry (An Internationl Journal Pure and Applied Chemistry), Vol (2), 2004.
6.Reverse HPLC method for the estimation of Isradipine in the Pharmaceutical dosage forms-Asian Journal of Chemistry, Vol.17 No 3 pp l406-1410 (2005).
7.Anti-microbial Activity of extractives of Millettia auriculata (Fabaceae) 56th Indian Pharmaceutical Congress, Kolkata.
8.Development and validation of a reverse phase HPLC method for the analysis of isradipine in pharmaceutical dosage forms Asian Journal of Chemistry 17 (2), 787(2005).
9.HPLC Determination of Telmisartan in Bulk and Pharmaceutical Formulations. Asian Journal of Chemistry, Vol.18 pp775-782(2006).
10.Determination of Ethamsylate in Pharmaceutical Preparations by Liquid Chromatography. Asian Journal of Chemistry, Vol.18 pp 783-787 (2006).
11.Quantitation of Floxuridine in K2EDTA Rat Plasma using HPLC Coupled with Tandem Mass Spectrometry, Published in Asian Journal of Chemistry; Vol.24, No.5(2012),2039-2041.
12.Method Development and Validation of Topotecan Hydrochloride in K2EDTA Human Plasma by Using HPLC Coupled with Tandem Mass Spectrometry, Published in Asian Journal of Chemistry; Vol24, No.8(2012),3617-3620.
13.LC-MS/MS Determination of Cabazitaxel in Rat Whole Blood on Dry Blood Spots, Published in Open Access Scientific Reports;
14.Liquid chromatography Tandem Mass Spectrometry Method for Determination of Docetaxel in K3EDTA Human plasma, International Journal of Pharmaceutical, Chemical and Biological sciences, Vol 4, Issue 3, Pages 711-716.
15.Stable Labeled Isotopes as Internal Standards: A Critical Review. Modern Applications in Pharmacy and Pharmacology. 1(2). MAPP.000508. 2017