Thursday , 29 June 2017

Tag Archives: HPLC

Analytical Method Development and Validation for the Simultaneous Estimation of Candesartan and Hydrochlorothaizide by RP-HPLC Method Pharmaceutical Dosage Form

Devanapelly Shashikantha Rao* Lecturer, Department of Chemistry, C.K.M. Arts and Science College, Warangal- 506006 Abstract A new method was established for simultaneous estimation of Candesartan cilexitil and Hydrochlorothiazide by RP-HPLC method. The chromatographic conditions were successfully developed for the separation of Candesartan cilexitil and Hydrochlorothaizide by using Zodiac sil C18 column (4.6×150mm)5µ, flow rate was 1ml/min, mobile phase ratio was ... Read More »

Formulation Development and optimization of Lyophilized product of an Anti Ulcer Drug

GY. Srawan kumar, V Deva Prasad, Raveendra, Harish K, Ann Jose, Reny Jose, Durga, Rachel mathai, Kempe gowda. Hindu College of Pharmacy, Guntur, Andhra Pradesh, India. Strides Arcolab Limited, Bangalore-560076, India Abstract The aim of present research work was to formulate an intravenous injection of Omeprazole sodium. Omeprazole drug is very slightly soluble in water. Hence in-situ conversion of Omeprazole ... Read More »

Stability indicating RP-HPLC Method Development and Validation for the Simultaneous Estimation of Olmesertan Medoxomil and Chlorthalidone in Pharmaceutical Formulation

Haribaskar*, T. Revathi, Ramesh Dhani Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Nellore, Andhra Pradesh, India A B S T R A C T A new method was established for simultaneous estimation of Olmesertan medoxomol and Chlothalidone by RP-HPLC method.  The chromatographic conditions were successfully developed for the separation of Olmesertan medoxomil and Chlorthalidone by using C18, 250 ... Read More »

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

Gobala Krishnan P*, Munisekhar V, Ranjit Singh B. Rathore Department of Pharmaceutical Chemistry, Vagdevi College of Pharmacy & Research Centre, Nellore, A.P, India A B S T R A C T A new method was established for simultaneous estimation of Atenolol and Nitrendipine by RP-HPLC method.  The chromatographic conditions were successfully developed for the separation of Atenolol and Nitrendipine by ... Read More »

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

Punna Venkateshwarlu*, CH. Shankar Department of Pharmaceutical Analysis, Vikas College of Pharmaceutical Sciences, Rayanigudem, Suryapet, Nalgonda, Telangana, India-508376 A B S T R A C T The chromatographic conditions were successfully developed for the separation of Metformin and Vildagliptin by using C18 Column (150 mm x 4.6 mm) 5 µm, flow rate was 1ml/min, mobile phase ratio was Methanol: Phosphate ... Read More »

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

Y. Krishna Reddy1, Dr. P.M Patel2 1Associate Professor, Bomma Institute of Pharmacy, Khammam, Telangana, India 2Principal, Kalol Institute of Pharmacy, kalol, Gujarat, India A B S T R A C T A new method was established for simultaneous estimation of Ezetamibe and Simvastatin by RP-HPLC method.  The chromatographic conditions were successfully developed for the separation of Ezetamibe and Simvastatin by ... Read More »

Analytical Method Development and Validation for the Estimation of Erlotinib Hydrochloride by RP-HPLC Method in Bulk and Pharmaceutical Dosage Form

Gobala Krishnan P*, Munisekhar V, Ranjit Singh B. Rathore Department of Pharmaceutical Chemistry, Vagdevi college of Pharmacy & Research centre, Nellore, Andhra Pradesh, India. A B S T R A C T The chromatographic conditions were successfully developed for the separation of Erlotinib hydrochloride by using the HPLC method for Erlotinib hydrochloride as per ICH Guide lines. Shimadzu LC-2010 series ... Read More »

Analytical Method Development and Validation for the Simultaneous Estimation of Beclomethasone Dipropionate and Clotrimazole by RP-HPLC Method in Bulk and Pharmaceutical Dosage Form

V. Padmaja*1, Dr. Y. Padmavathi2 1Dept. of Pharmaceutical Chemistry, G. Pullareddy College of Pharmacy, Hyderabad, Telangana, India 2Professor, G. Pullareddy College of Pharmacy, Hyderabad, Telangana, India A B S T R A C T The chromatographic conditions were successfully developed for the separation of Beclomethasone dipropionate and Clotrimazole by using column C18 [Macherey-Nagel Nucleosil], 4.6x250mm, 5 microns flow rate was ... Read More »

Stastical Comparision, Method Development and Validation of High Performance Liquid Chromatography for estimation of Cifixime Trihydrate and Potassium Clavunate in bulk and combine tablet dosage form

1A. B. Patel*, 2Dr M. M. Patel, 3Dr B. N Suhagiya, 4Dr B. V. Patel, 5Dr. A. B. Patel  1Assistant Professor, Department of pharmaceutical chemistry, Kalol institute of Pharmacy, Kalol, India 2Director and   Principal of Shankersinh Vaghela Bapu Institute of Pharmacy, India 3Dean at Faculty of Pharmacy, Dharmsinh Desai University, Nadiad 4Professor, Department of Microbiology, Guajrat University, India 5 College ... Read More »

Analytical Method Development and Validation for the Simultaneous Estimation of Tranexamic acid and Ethamsylate by RP-HPLC Method in Bulk and Pharmaceutical Dosage Form

D. Sravanthi*, V. Pavan Kumar, M. Gobinath, V. Haribaskar, Ramesh Dhani, G. Kumari Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Nellore, Andhra Pradesh, India A B S T R A C T The chromatographic conditions were successfully developed for the separation of Tranaxamic acid and Ethamsylate by using Thermosil C18 column (4.6×100mm) 5µ, flow rate was 1ml/min, mobile ... Read More »

Scroll To Top