B.PHARM DISSERTATION PROJECT
YEAR |
DISSERTATION TITLE |
GUIDE NAME |
|
2018 |
Formulation and Development of a Validated UV Spectrophotometric Method for Estimation of Brexpiprazole Bulk and Formulated Dosage Form | Caroline Grace.A |
|
2017 |
UV Spectrophotometric Method Development For Simultaneous Estimation of Paracetamol, Aceclofenac and Serratiopeptidase in Tablet Dosage form | Caroline Grace.A |
|
2016 |
Development and Validation of UV Spectroscopic Estimation of Imatinib in Tablet Dosage Form | Caroline Grace.A |
|
2016 |
Development and Validation of UV Spectroscopic Method for the Determination of Thiocolchicoside in Parenteral Dosage Form | Caroline Grace.A |
| 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