Dissertation projects

B.PHARM DISSERTATION PROJECT

YEAR DISSERTATION TITLE GUIDE NAME
2013  UV SPECTROPHOTOMETRIC ESTIMATION OF CEFUROXIME AXETIL IN BULK AND ITS TABLET FORM Dr.M.JAGADEESWARAN 
     

 M.PHARM DISSERTATION PROJECT

YEAR REG.NO DISSERTATION TITLE GUIDE NAME
2012 26104321 RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF METFORMIN HCL AND VOGLIBOSE IN BULK AND ITS PHARMACEUTICAL DOSAGE Dr.T.PRABHA
2012 26104322 STABILITY INDICATING METHOD DEVELOPMENT AND VALIDATION OF PRALIPERIDONE BY HPLC METHOD Dr.M.JAGADEESWARAN
2012 26104323 SIMULTANEOUS METHOD DEVELOPMENT AND VALIDATION OF IBUPROFEN AND METHOCARBOMOL IN BULK AND FORMULATION BY RP-HPLC DR.T.PRABHA
2011 26093371 NEW RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF RIZATRIPTAN BENZOATE IN TABLET FORM Dr.M.JAGADEESWARAN
2011 26093373 SIMULTANEOUS ANALYSIS OF ATORVASTATIN CALCIUM AND TELMISARTAN FROM THEIR PHARMACEUTICAL DOSAGE FORMS Dr.T.SIVA KUMAR
2011 26093374  METHOD DEVELOPMENT AND METHOD VALIDATION FOR SIMULTANEOUS ESTIMATION OF RIFAMPICIN AND ITS METABOLITE (DESACETYL RIFAMPICIN) IN HUMAN PLASMA BY USING LC-MS/MS Dr.T.PRABHA 
2011  26093375  ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF GLUCOSAMINE SULPHATE AND CHONDROITIN SULPHATE SOFTLET (ENROBED TABLET) BY HPLC Mr.R.RAJAVEL
2011  26093376  A SIMPLE AND QUICK STABILITY INDICATING METHOD FOR ASSAY OF ANASTROZOLE IN LOW DOSE ANASTROZOLE TABLETS BY RP-HPLC Dr.T.PRABHA
2011 26093377  DEVELOPMENT AND VALIDATION OF BIOANALYTICAL METHOD FOR THE ESTIMATION OF URSODEOXYCHOLIC ACID IN HUMAN PLASMA BY LC-MS/MS Dr.T.SIVA KUMAR
2011  26093378  METHOD DEVELOPMENT AND VALIDATION FOR QUANTITATIVE DETERMINATION OF TAMSULOSIN HYDROCHLORIDE IN TAMSULOSIN HYDROCHLORIDE PELLETS 0.2% BY RP-HPLC  Dr.M.JAGADEESWARAN
2011 26093379 DEVELOPMENT AND VALIDATION OF BIOANALYTICAL METHOD FOR THE SIMULTANEOUS QUANTITATION OF DILTIAZEM AND ITS METABOLITES (N-DESMETHYL DILTIAZEM, DESACETYL DILTIAZEM) IN HUMAN K2 EDTA PLASMA BY USING LC-MS/MS Dr.T.SIVA KUMAR 
2011 26093380 DEVELOPMENT AND VALIDATION OF STABILITY INDICATING UPLC METHOD FOR SIMULTANEIOUS ESTIMATION OF ABACAVIR, LAMIVUDINE AND ZIDOVUDINE IN PHARMACEUTICAL DOSAGE FORM Mr.R.RAJAVEL
2010 26083371 ESTABLISHMENT OF METHOD TO STUDY THE EFFECT OF S-AMLODIPINE ON GLYCATION OF PROTEIN BY MALDI-TOF-MS Dr.M.JAGADEESWARAN
2010 26083372 DEVELOPMENT OF ANALYTICAL METHOD FOR SIMULTANEOUS ESTIMATION OF RAMIPRIL AND VALSARTAN IN COMBINED DOSAGE FORM Dr.T.SIVA KUMAR
2010 26083373 ANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF RELETED SUBSTANCES AND DISSOLUTION METHOD FOR BETAMETHASONE ACETATE AND BETAMETHASONE SODIUM PHOSPHATE INJECTABLE SUSPENSION USING HPLC AND TYPE 4 DISSOLUTION APPARATUS Dr.T.SIVA KUMAR
2010 26083374 BIOANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF ANTI-ARRTHYMIC DRUG IN HUMAN PLASMA BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY - TANDEM MASS SPECTROMETRY Mr.R.RAJAVEL
2010 26083375 METHOD DEVELOPMENT FOR THE STUDY OF EFFECT OF ATENOLOL ON PROTEIN GLYCATION BY MALDI-TOF-MS Dr.T.PRABHA
2010 26083376 RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF SIMULTANEOUS ESTIMATION OF THIOCOLCHICOSIDE AND ETORICOXIB IN TABLET DOSAGE FORM Mr.R.RAJAVEL
2010 26083377 METHOD DEVELOPMENT AND VALIDATION FOR THE ASSAY OF GEMCITABINE HYDROCHLORIDE IN PHARMACEUTICAL DOSAGE FORMS BY RP-HPLC Dr.T.SIVA KUMAR
2010 26083378 RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF SIMULTANEOUS ESTIMATION OF VITAMINS B1, B2, B3 AND B6 IN CAPSULE FORMATION Dr.M.JAGADEESWARAN
2010 26083379 A SPECIFIC, ACCURATE, PRECISE, VALIDATED AND REPRODUCIBLE HIGH PERFORMANCE LIQUID CHROMATIGRAPHY METHOD FOR THE ESTIMATION OF ROSUVASTATIN (RST) Dr.T.PRABHA
2010 26083380 RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR THE ESTIMATION OF LOSARTAN POTASSIUM AND AMLODIPINE BESYLATE IN BULK AND ITS PHARMACEUTICAL DOSAGE FORM Dr.M.JAGADEESWARAN
2009 26073371 STABILITY-INDICATING ASSAY METHOD DEVELOPMENT AND VALIDATION FOR QUETIAPINE HEMIFUMERATE BY USING HPLC Mr.R.RAJAVEL
2009 26073372 ESTIMATION OF PARACETAMOL, ACECLOFENAC AND CHLORZOXAZON BY RP-HPLC METHOD AND ITS VALIDATION Mr.G.RATHINAVEL
2009 26073373 METHOD DEVELOPMENT AND VALIDATION FOR ESTIMATION OF LANSOPRAZOLE BY USING ESOMEPRAZOLE AS AN INTERNAL STANDARD IN HUMAN PLASMA USING LC-MS/MS TECHNIQUE Mr.M.GANESH
2009 26073374 SIMULTANEOUS ESTIMATION OF DIACERCIN AND ACECLOFENAC IN TABLETS BY RP-HPLC METHOD AND ITS VALIDATION Dr.M.JAGADEESWARAN
2009 26073375 METHOD DEVELOPMENT AND VALIDATION FOR MELOXICAM CONTENT IN HUMAN PLASMA BY USING LC-MS/MS Mr.M.GANESH
2009 26073376 METHOD DEVELOPMENT AND VALIDATION FOR AZITHROMYCIN CONTENT IN HUMAN PLASMA BY USING LC-MS/MS Mr.R.RAJAVEL
2009 26073377 SIMULTANEOUS ESTIMATION OF AMLODIPINE BESYLATE AND NEBIVOLOL HYDROCHLORIDE IN TABLETS BY RP-HPLC METHOD AND ITS VALIDATION Dr.M.JAGADEESWARAN
2009 26073378 METHOD DEVELOPMENT AND VALIDATION FOR NITAZOXANIDE IN TABLET USING RP-HPLC  Ms. J.VALARMATHY
2009 26073379 HPLC METHOD DEVELOPMENT AND VALIDATION OF ROSUVASTATIN CALCIUM IN TABLET DOSAGE FORM Dr.T.SIVA KUMAR
2009 26073380    

 

 

 

 

 

 

 

The following are the dissertation projects carried out in the department of Pharmaceutical Analysis:

  • Establishment of Method to Study the Effect of S-Amlodipine on Glycation of Protein By MALDI-TOF-MS
  • Development of Analytical Method for Simultaneous Estimation of Ramipril & Valsartan in Combined Dosage Form
  • Analytical Method Development and Validation of Related Substances and Dissolution Method for Betamethasone Acetate and Betamethasone Sodium Phosphate Injectable Suspension Using HPLC and Type 4 Dissolution Apparatus
  • Bio Analytical Method Development and Validation of Prepafenone in Human Plasma by High Performance Liquid Chromatography – Tandem Mass Spectroscopy
  • Method Development for the Study of Effect of Atenolol on Protein Glycation By MALDI-TOF-MS
  • RP-HPLC Method Development and Validation of Simultaneous Estimation of Thiocolchicoside and Etoricoxib in Tablet Dosage Form
  • Method Development and Validation for the Assay of Gemcitabine Hydrochloride in Pharmaceutical Dosage Forms by RP-HPLC
  • RP-HPLC Method Development and Validation of Simultaneous Estimation of Vitamin B1,B2,B3 And B6 in Capsule Formulation
  • A Specific, Accurate, Precise, Validated and Reproducible High Performance Liquid Chromatography Method for the Estimation of Rosuvastatin
  • RP-HPLC Method Development and Validation for the Estimation of Losartan Potassium and Amlodipine Besylate in Bulk and its Pharmaceutical Dosage Form
  • Stability Indicating Method Development and Validation for the Estimation of Gatifloxacin in Ophthalmic Dosage Form by Using RP-HPLC Method.
  • Method Development and Validation for the Estimation of Lapatinib Ditosylate in Tablet Dosage Form by Ultraviolet Spectroscopy and RP-HPLC
  • Simultaneous Estimation of Lamivudine and Zidovudine in Bulk Dosage Form by UPLC Method
  • Stability Indicating Method Development and Validation of Efavirenz in Bulk Dosage Forms Using RP-HPLC
  • Development and Validation of Stability Indicating RP-HPLC Method for the Estimation of Dasatinib in Tablet Dosge Form
  • Method Development and Validation by RP – HPLC Method for the Simultaneous Estimation of Levetiracetam and its Preservatives in Oral Liquid Dosage Form
  • Method Development and Validation for the Simultaneous Estimation of Abacavir and Lamivudine in Tablet Dosage Form by RP – HPLC
  • Bioanalytical Method Development and Validation for the Quantitation of Valsartan in Rat Plasma by Using LC – MS/MS
  • RP-HPLC Method Development and Validation for the Simultaneous Estimation of Ampicillin Trihydrate and Dicloxacillin Sodium in its Solid Dosage Forms
  • Development and Validation of Stability Indicating RP- HPLC Method for the Simultaneous Estimation of Hydrochlorthiazide and Metoprolol in Tablet Dosage Forms
  • Method Development and Validation for Simultaneous Estimation of Metformin Hydrochloride and Sitagliptin in Pharmaceutical Dosage Form by RP - HPLC
027490