Appa Rao Kommaraju M Ch

Appa Rao Kommaraju M Ch

Professor, Chemistry, GSS , VSP

Education
Ph. D.
Email ID
mkommara@gitam.edu
Education
Ph. D.

Education

Degree Name Institute & College name Year of Graduation/Award
Doctor of Philosophy School of Chemistry 1994
Master of Science School of Chemistry 1983
Bachelor of Science Mrs. A.V.N. College 1980

Experience

Designation Organization From Date To Date
Professor GITAM Deemed to be University 12-12-2008 31-07-2019
Associate Professor GITAM Engineering college 13-07-2004 11-12-2008
Assistant Professor with Senior scale GITAM Engineering college 01-04-1998 12-07-2004
Assistant Professor GITAM Engineering college 08-11-1994 31-03-1998
Teaching Assistant GITAM Engineering college 23-01-1992 07-11-1994

Enantioselective synthesis of new phenylpropanoid Isolated from Walsura trifoliateAsian Journal of Chemistry , Scopus, -2019, 31, 2042-2046

New phenolic Constituents from bark of Walsura trifoliateJournal of Pharmacognosy and Phytochemistry, Google scholar, -2017, 6, 1314-1316

A rapid separation technique for the determination of potential impurities present in Levodopa, Carbidopa and Entacapone in fixed dose combination drug product using trifunctionally bonded phase ethylene bridged sorbent column with smaller ionpair reagentJournal of Liquid Chromatography & Related Technologies, Scopus, -2015, 38, 1073-1087

HPLC method for simultaneous determination of potential impurities of Norgestimate andEthinyl Estradiol in combination drug product Using sub2m columnJournal of Liquid Chromatography & Related Technologies, Scopus, -2015, 38, 1014-1025

Method Development and Validation for the Determination of Four Potential Impurities Present in Darunavir Tablets by Reverse PhaseUltraPerformance Liquid Chromatography.Journal of Liquid Chromatography & Related Technologies, Scopus, -2015, 38, 1236-1246

Development of Stability Indicating Related Substance Method for Fingolimod and their Validations StudiesInventi Rapid Pharm Analysis & Quality Assurance, Google scholar, -2015, 2014, 1-6

A sensitive RPHPLC method development and validation for the simultaneous estimation of atorvastatin calcium, fenofibrate, and orlistat in tablet dosage form International Journal of Pharmaceutical Research & Analysis , Google scholar, -2014, 4, 7-13

A new and stability indicating liquid chromatographic method for the determination of dabigatran in bulk drug and pharmaceutical dosage formAnalytical Chemistry An Indian Journal, Google scholar, -2014, 14, 264-273

Ultra Performance Liquid Chromatography Method for the Determination of Degradation Impurities of Naftopidil in Naftopidil Orally Dispersible TabletsAmerican Journal of Pharm Tech Research , Google scholar, -2014, 4, 685-700

HPLC Method for Simultaneous Determination of Chlorpheniramine, Ibuprofen and Pseudoephedrine in FixedDose Combination using Multiple Column Chemistries under Qbd ConceptAmerican Journal of Pharm Tech Research , Google scholar, -2014, 4, 917-937

A Sensitive UPLC Method Development and Validation with LCMS Compatible for the Determination of 1Deoxynojirimycin In Mulberry Leaves using Fluorescence DetectionAmerican Journal of Pharm Tech Research , Google scholar, -2014, 4, 423-436

Development and Validation of a Novel Ultra Performance Liquid Chromatography Method for Dissolution of Paricalcitol in Paricalcitol Soft Gelatin CapsulesAmerican Journal of Pharm Tech Research , Google scholar, -2014, 4, 720-731

Development and Validation of a new simple and Stability indicating RPHPLC Method for the determination of Tetrabenazine and its forced degradation impurities in Bulk Drug and Pharmaceutical Dosage formInternational Journal of PharmTech Research, Google scholar, -2014, 6, 1003-1010

Devolpment and validation of simple stability indicating RPHPLC method for analysis of Saxagliptin and its forced degradation impurities in bulk drug and pharmaceutical dosage formInt. J. Res. Dev. Pharm. L. Sci, Google scholar, -2014, 3, 993-1003

Development and Quantification in Ivacaftor and Related Impurities Using Liquid Chromatography TechniqueInventi Rapid Pharm Analysis & Quality Assurance , Google scholar, -2014, 2014, 1-7

Method Development of Related Substance in Dabigatran and its Validation Followed by its Stability Indicating Study Using the HPLC TechniqueInventi Rapid Pharm Analysis & Quality Assurance, Google scholar, -2014, 2014, 1-6

Development and validation of a new and stability indicating LC method for analysis of Pinaverium bromide in bulk drug and pharmaceutical Dosage formPharm Science Monitor , Google scholar, -2014, 5, 164-175

Development and validation of RP HPLC method for determination of Raltegravir and its impurities in bulk drug and dosage formsPharm Science Monitor , Google scholar, -2014, 5, 187-196

Method Development and Validation for the determination of potential impurities present in Azilsartan medoxomil tablets by Reverse Phase Ultra Performance Liquid ChromatographyAnalytical Chemistry Letters, Google scholar, -2014, 4, 287-301

Development and validation of a new simple and stability indicating RPHPLC method for the determination of Vemurafenib in presence of degradant productsDer Pharma Chemica, Scopus, -2013, 5, 189-198

Development and validation of stability indicating method for determination of Lurasidone in bulk drug and pharmaceutical dosage form by HPLCInt. Journal of Pharmaceutical Research & Development, Google scholar, -2013, 5, 103-114

New Reverse Phase HPLC Determination of Imatinib in bulk and formulationJournal of Pharmacy Research, Google scholar, -2012, 5, 3923-3925

Quantification of residual elemental sulphur present in pharmaceutical ingredients by HPLC and UPLCInt. J. Res. Chem. Env., , Google scholar, -2012, 2, 270-274

New visible spectrometric determination of Gemifloxacin in its pure form Int. J. Pharm. Pharmaceut. Sci., , Scopus, -2012, 4, 618-621

Quantification of residual elemental Sulphur present in pharmaceutical ingredients byHPLC and UPLC Int. J. Adv. Pharm. Biol.Chem , Google scholar, -2012, 1, 121-127

Determination of Aripiprazole in Bulk Formulation by Visible Spectrophotometric MethodsAsian Journal of Research in Chemistry, Google scholar, -2011, 4, 1752-1754

New method development and validation of Tadalifil using uv visible spectrophotometer Int. J. Res. Revs. Pharm. App. Sci., Google scholar, -2011, 1, 172-178

Determination of Flurbiprofen pellets 57% using drug release method by UV Rasayan J Chemistry, Scopus, -2009, 2, 418-420

Marine Terpenes and Terpenoids part 19, Structure of Tetracyclic Norcembranolide Derivative Isolated from the Soft Coral Sinularia dissectaJ. Chem. Res.(S), Scopus, -1995, NA, 188

Isolation of Loba8, 10, 15triene13, 17, 18triol17, 18diacetate from a Soft Coral Lobophytum species of the Andaman and Nicobar IslandsIndian J. Chem, Scopus, -1995, 34B, 1071-1073

Marine Sterols Part 29. Isolation of New polyhydroxysterol and Steroidal glycosides from the soft coral Sinularia gibberosaJ. Chem. Res. (S), , Scopus, -1994, 1, 140

Marine sterols part 30. Isolation of 24Methylenecholestane 1, 3, 5, 6, 11 pentaol and its 11monoacetate from the Andaman Sea Soft Coral Sinularia dissectaJ. Chem. Res. (S), , Scopus, -1994, 1, 180

24Methylenecholest4ene3, 6diol from a Soft Coral Sinularia ovispiculata of the Andaman and Nicobar IslandsIndian J. Chem Section B, Scopus, -1994, 33B, 806

Seminar name Organized by Venue Start date End date Title of the paper presented Role Co presenter
National School of Chemistry, Andhra University School of Chemistry, Andhra University, Visakhapatnam 27-Mar-2000 30-Mar-2000 Participated
National College of Engineering GITAM College of Engineering, GITAM 02-May-1999 03-May-1999 Participated
National School of Chemistry, Andhra University School of Chemistry, Andhra University, Visakhapatnam 11-Jul-1997 13-Jul-1997 Participated
Seminar name Organized by Venue Start date End date Title of the paper presented Role Co presenter
Title of the thesis Name of the student Name of the college / university Major subject area Year of admission Type of admission Thesis specification
_ L V Ramana GITAM Natural Products 2014 Part time PhD
Title of the thesis Name of the student Name of the college / university Major subject area Year of admission Type of admission Thesis specification
Title of the thesis Name of the student Name of the college / university Major subject area Year of admission Type of admission Thesis specification
New analytical studies on UPLC profile of selected active pharmaceutical ingredients and Impurities J Rudra Prasada Reddy Method development and Validation 2011 Part time PhD
Development and validation of analytical methods for related substances from active pharmaceutical ingredients using HPLC technique M. Balajee Method development and Validation 2011 Part time PhD
New validated liquid chromatographic and spectrophotometric methods for the determination of selected pharmacodynamic and chemotherapeutic drugs SVV Dhanu Radha Method development and Validation 2006 Part time PhD
Title Type Organized by Venue Start date End date Role
Refresher Course in Chemistry Training of tutors Academic Staff College, AU Andhra University, Visakhapatnam 19-Aug-2002 08-Sep-2002 Participated
Refresher Course in Chemistry Training of tutors ASC, AU, Visakhapatnam Academic Staff college, Andhra University 21-May-2001 10-Jun-2001 Participated
Refresher Course on Environmental Impact analysis Auditing and Environmental modeling Training of tutors ISTE and RMC, Andhra University Resource Mobilization Cell, Andhra University 04-Sep-2000 28-Sep-2000 Participated
Title Type Organized by Venue Start date End date Role
Organization name Membership category Membership type
Indian Chemical Society ICS Life Member
Indian Science Congress Association Life Member
Indian Association of Chemistry Teachers IACT LM Life Member
Indian Society for Technical Education Life Member