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Faculty of Pharmacy: Recent submissions

Now showing items 1-20 of 222

Development and Validation of UV Spectrophotometric and RPHPLC Methods for Estimation of Esomeprazole Magnesium Trihydrate and Naproxen in bulk & tablet dosage form

Suthar, Jigarkumar (Parul University, 2012)

Naproxen and Esomeprazole Magnesium Trihydrate are used in combination for treatment of osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. The present work deals with two simple, precise and economical ...
Development and Validation of UV Spectrophotometric and RP-HPLC Methods for Estimation of Aliskiren Hemifumarate and Valsartan in bulk and Pharmaceutical Dosage Form

Gorwadia, Hitesh (Parul University, 2012)

A First order derivative spectroscopy and RP-HPLC methods were developed and validated for simultaneous estimation of Aliskiren hemifumarate and Valsartan in bulk and synthetic mixture. A simple and easy UV spectrophotometric ...
Process validation of Pantoprazole and Rabeprazole Lyophilized Product

Desai, Avni (Parul University, 2012)

Since process validation is essential for fulfillment of regulatory requirements and quality, the prospective validation of the new manufacturing process of lyophilized Pantoprazole and Rabeprazole injections I.P was carried ...
Stability Indicating RP-HPLC Method Development and Validation for Psychostimulant Drugs in Syrup Dosage Form

Patel, Krupaben (Parul University, 2012)

A Stability Indicating RP-HPLC method was developed and validated for estimation of Psychostimulant drugs in syrup dosage form. The RP-HPLC method has shown adequate separation of drug A from its degradation products. The ...
Process Validation of Ofloxacin film coated tablet and Diazepam

Goswami, Smita (Parul University, 2012)

The aim of present project work was to carryout Concurrent validation of Ofloxacin film coated tablet and prospective process validation of Diazepam tablet. For concurrent validation of Ofloxacin film coated tablet. Three ...
Development & Validation of UV-Spectroscopic & RP-HPLC Method for Simultaneous Estimation of Levosulpiride & Rabeprazole Sodium in bulk and tablet dosage form

Thakkar, Divya (Parul University, 2012)

A simple, accurate and precise UV Spectrophotometric methods and RP-HPLC method have been developed and validated for simultaneous estimation of Levosulpiride and Rabeprazole Sodium in bulk and tablet dosage form. Two UV ...
Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Metoprolol Succinate and Olmesartan Medoxomil in Bulk and Tablet Dosage Form

Savalia, Rajesh (Parul University, 2012)

A simple, accurate, precise and stability Indicating RP-HPLC method was developed and validated for simultaneous estimation of metoprolol succinate and olmesartan medoxomil in bulk and tablet dosage form. The RP-HPLC ...
Method Development and Validation for the Determination of Related Substances of Ezetimibe in Tablet Dosage Form

Maheshwari, Vipul (Parul University, 2012)

The aim of present work was to develop and validate a accurate, precise and sensitive method for the determination of related substances of Ezetimibe in tablet dosage form. The RP-HPLC method has shown adequate separation ...
Development and validation of stability indicating rp-hplc method for estimation of related substances of esomeprazole in capsule dosage form

Patel, Chinmay (Parul University, 2012)

A sensitive, accurate and precise method has been developed for the estimation of related substances of Esomeprazole in capsule dosage form. The RP-HPLC method has shown adequate separation for Esomeprazole and its Impurities ...
Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Ofloxacin and Cefpodoxime proxetil in Bulk and Tablet Dosage Form

Patel, Reemaben (Parul University, 2012)

A simple, accurate, precise and stability Indicating RP-HPLC method was developed and validated for simultaneous estimation of ofloxacin and cefpodoxime proxetil in bulk and tablet dosage form. The RP-HPLC method has shown ...
Development and Validation of RP-HPLC Method & Dissolution Profiling of Tianeptine Sodium in its Pharmaceutical Dosage Form

Vadgama, Bhumit (Parul University, 2012)

The purpose of this work is to develop a sensitive, selective, and validated RP-HPLC assay of Tianeptine Sodium in bulk drug and tablet form. Tianeptine Sodium was analyzed on INERTSIL ODS C18 column using isocratic ...
Development and Validation of Stability Indicating RP-HPLC Method for Estimation of Related substances of Cevimeline Hydrochloride in Capsule Dosage Form

Adhvaryu, Harsh (Parul University, 2012)

A specific, accurate, precise, sensitive and stability indicating RP-HPLC method was developed and validated for estimation of related substances of Cevimeline Hydrochloride in Capsule dosage form. The RP-HPLC method showed ...
Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Lafutidine and Domperidone in Bulk and Pharmaceutical Dosage Form.

Chokshi, Pooja (Parul University, 2012)

A sensitive, accurate and precise method was developed and validate for the simultaneous estimation of Lafutidine and Domperidone in capsule dosage form. The RP-HPLC method had shown adequate separation for Lafutidine and ...
Development and Validation of RP-HPLC method for the determination of impurity profile of Desvenlafaxine Extended Release Tablet

SANGHAVI, NEMISH (Parul University, 2012)

A accurate, rapid, precise and specific RP-HPLC method was developed for the determination of impurity profile of Desvenlafaxine in Desvenlafaxine ER tablet. Both known impurities i.e., venlafaxine Base and ODV Dimer ...
Analytical Method Development and Validation for Simultaneous Estimation of Cefixime and Azithromycin in Bulk and Their Combined Dosage Form

Rokad, Jenisha (Parul University, 2012)

A simple, accurate and precise UV Spectrophotometric methods and RP-HPLC method was developed and validated for simultaneous estimation of Cefixime and Azithromycin in bulk and tablet dosage form. Two UV spectrophotometric ...
Prospective and Concurrent Process Validation of Ranitidine Film Coated Tablet BP 150 mg and Amlodipine Tablet BP 10 mg

Gupta, Neha (Parul University, 2012)

The aim of present project work was to carryout prospective validation of ranitidine film coated tablet BP 150 mg and concurrent process validation of amlodipine tablet BP 10 mg. For both of the process validation , three ...
Development and validation of stability indicating rp-hplc method for simultaneous estimation of sitagliptin and simvastatin in bulk And pharmaceutical dosage form

Patel, Krupali (Parul University, 2012)

Objective: The objective is to develop and validate stability indicating reverse-phase HPLC method for estimation of Sitagliptin and Simvastatin in bulk and pharmaceutical dosage form. Experimental Work: The proposed ...
Formulation, characterization and evaluation of wafer containing antimicrobial agent for wound infection

SOLANKI, KHUSHBU (Parul University, 2018-05)

The aim of present research work is to formulate wafer containing antimicrobial agent for wound infection. Wound is an infectious diseases which can be the result of colonization of the body by various microorganisms. ...
Nanoliposomal topical formulation for increasing safety and combating microbial drug resistance in leprosy

SHAH, DEEP (Parul University, 2019-04)

The aim of the present investigation was to develop and evaluate nanoliposomal topical spray for the improved treatment of leprosy. Dapsone and chaulmoogra oil can improve the leprosy condition if given in the form of ...
Analytical method development and validationfor simultaneous estimation of rosuvastatin calcium, clopidogrel bisulphate and aspirin in pharmaceutical dosage form

MYAKAM, DIVYABEN (Parul University, 2016-04)

A First order derivative spectroscopic method and RP-HPLC method were developed and validated for simultaneous estimation of Rosuvastatin Calcium, Clopidogrel Bisulphate and Aspirin in Pharmaceutical Dosage form. First ...

Now showing items 1-20 of 222

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