Tuesday , 19 October 2021

Tag Archives: Validation

RP-HPLC method for the Simultaneous estimation of Ezitimibe and Simvastatin in bulk and it’s tablet dosage form

C. Karuppasamy*1, Sanjay Kumar Jain2 1Safa College of Phrmacy, Kurnool, Andhra Pradesh, India 2Department of Pharmaceutical Analysis, Bundelkhand University, Jhansi, U.P, India A B S T R A C T The present attempt was made to development and validation of new RP-HPLC method for the simultaneous estimation of Ezitimibe and Simuvastatin in bulk and tablet dosage form. The chromatographic separation ... Read More »

Simultaneous RP-HPLC method for the estimation of Clopidogrel and Atorvastatin in bulk and its tablet dosage form

C. Karuppasamy*1, Sanjay Kumar Jain2 1Safa College of Pharmacy, Kurnool, Andhra Pradesh, India 2Department of Pharmaceutical Analysis, Bundelkhand University, Jhansi, U.P, India A  B  S  T  R A C T The aim of present research work simple, precise, accurate and robust RP-HPLC method for the simultaneous estimation of Clopidogrel and Atorvastatin in bulk and tablet dosage form. The chromatographic separation ... Read More »

Simultaneous RP-HPLC Method for the Quantification of Durnavir and Ritonavir in bulk and it’s Pharmaceutical Dosage form

Y. Suresh*1, Sanjay Kumar Jain2 1Safa College of Pharmacy, Kurnool, Andhra Pradesh, India 2Department of Pharmaceutical Analysis, Bundelkhand University, Jhansi, U.P, India A  B  S  T  R A C T The aim of present research work to develop and validated RP-HPLC method for the simultaneous estimation Durnavir and Ritonavir in bulk and pharmaceutical dosage form. The chromatographic separation was achieved ... Read More »

Development of Simple, Reliable, Rugged, Specific and Stability Indicating HPLC Methods for Quantification of Impurities in Canagliflozin

R. Suresh1*, Dr. Satyavir Singh 2, K. Subhash Chander Reddy3 1Research Scholar, 2Department of Science, OPJS University, Churu, Rajasthan. 2Department of Science, OPJS University, Churu, Rajasthan. 3Director Honour lab R&D, Bonthapalli, Hyderabad, Telangana. A  B  S  T  R A C T The aim of present research work development of simple, reliable, rugged, specific and stability indicating HPLC methods for quantification ... Read More »

Development and Validation of UV-Spectroscopic Method for Estimation of Formoterol in Bulk and Pharmaceutical Dosage Form

K. Surendra*, P. Penchalamma, G. Vikas, C. Dileep Reddy, S. Chaitanya Rao’s College of Pharmacy, Chemudugunta, Venkatachalam, Nellore, Andhra Pradesh-524320 A B S T R A C T The aim of present research work method development and validation for the quantification of Formoterol in bulk and its pharmaceutical dosage form by using UV spectroscopy. The solvent employed for this method ... Read More »

UV-Spectrophotometric Method for the Determination of Azilsartan Medoxomil in Bulk and Its Dosage Form

K. Surendra*, M. Vinitha, B. Siva Shankar Reddy, B. Vinay, G. Srinivasulu Rao’s College of Pharmacy, Chemudugunta, Venkatachalam, Nellore, Andhra Pradesh-524320 A B S T R A C T The present research work was broadly focused on the estimation of Azilsartan medoxomil in bulk and its formulation by using four UV spectrophotometric methods like Zero order spectroscopy(Method-A), Area under curve ... Read More »

Method Development and Validation for the Simultaneous estimation of Velpatasvir and Sofosbuvir in tablet dosage form by using RP–HPLC

M. Anusha*, B.V. Ramana, G. Nagarajan Dr. K.V. Subba Reddy Institute of Pharmacy, Kunrool, Andhra Pradesh, India A B S T R A C T The present research work mainly focused on method development and validation for the simultaneous estimation of velpatasvir and sofosbuvir in tablet dosage form by using RP-HPLC. Chromatographic separation was carried on YMC C18 column (4.6*150mm, ... Read More »

Development of New RP-HPLC method for the estimation of Glycopyrrolate and Formoterol fumarate in the tablet dosage form

Damam Vidya*, B.V. Ramana, G. Nagarajan Dr. K.V. Subba Reddy Institute of Pharmacy, Kunrool, Andhra Pradesh, India A B S T R A C T The present research work mainly focused on method development and validation for the simultaneous estimation of Glycopyrrolate and Formeterol fumarate in tablet dosage form by using RP-HPLC. Chromatographic separation was achieved on Xterrra C18 column ... Read More »

RP-HPLC Method Development and Validation for Simultaneous Estimation of Dasatinib and Lenvatinib in Its active Pharmaceutical Ingredient and Pharmaceutical Dosage Forms

B. Yamuna Rani1, Dr. D. Naresh2, Dr. Gampa Vijay Kumar3* 1KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India. 2KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India. 3Professor and Head, Dept. of Pharmacy, KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India. A  B  S  T  R A C T A new method ... Read More »

Analytical Method Development and Validation for the Simultaneous Estimation of Ranitidine and Dicyclomine in Bulk and Pharmaceutical Dosage Form by RP-HPLC

K. Surendra*, V. Gunasekaran, K. Venkata Arun Teja Rao’s College of Pharmacy, Chemudugunta, Venkatachalam, Nellore, Andhra Pradesh-524320 A  B  S  T  R A C T A rapid and precise reverse phase high performance liquid chromatographic method has been developed for the validated of Ranitidine and Dicyclomine, in its pure form as well as in tablet dosage form. Chromatography was carried ... Read More »

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