Wednesday , 20 January 2021

Tag Archives: RP-HPLC

Analytical Method Development and Validation for the Determination of Brinzolamide and Brimonidine Using Reverse Phase HPLC Method in Bulk and Pharmaceutical Dosage Form

Dr R. Vani1*, Amena Samreen2, Humera Tabassum3, Dr M.sunitha4* 1Head of Department, Pharmaceutical Analysis and QA, Shadan Women’s College of Pharmacy, Hyderabad. 2Post-Graduate Student, Shadan Women’s College of Pharmacy, Hyderabad. 3Post-Graduate Student, Shadan Women’s College of Pharmacy, Hyderabad. 4Principal, Shadan Women’s College of Pharmacy, Hyderabad. ABSTRACT In RP-HPLC method, the conditions were optimized to obtain an adequate separation of eluted ... Read More »

Simultaneous Estimation of UV Spectroscopy and Method Development and Validation for Lansoprazole and Domperidone by RP-HPLC

Sanju Srinivas1, Marium Nazneen2 1Associate Professor Department of Pharmacy, Ganga Pharmacy College, Nizamabad, Telangana 2Department of Pharmaceutical Analysis, Ganga Pharmacy College, Nizamabad, Telangana ABSTRACT A new method was established for simultaneous estimation of Lansoprazole and Domperidone by RP-HPLC method. The chromatographic conditions were  successfully developed  for  the  separation  of  Lansoprazole and Domperidone by using Xterra C18 5µ m (4.6*250mm) column, ... Read More »

RP HPLC Method Development and Validation of Bicaultamide and Simvastatin in Bulk and Pharmaceutical Dosage Forms

C. Srinavya*1, P. Sowjanya2, Dr. Gampa Vijaya Kumar3 1,2KGR 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 was established for simultaneous estimation of Bicalutamide and Simvastatin by RP-HPLC method.  The chromatographic ... Read More »

Analytical Method Development and Validation for Sacubitril and Valsartan in Combine Pharmaceutical Dosage Forms by RP-HPLC

G. Madhavi1, S. Sravani1, G. Nikithareddy1, V. Mounika1, B. Divya1, M. Chaithanya*1, Bijjiga Sravanthi2 1Bojjam Narasimhulu Pharmacy College, Sayeedabad, Hyderabad, Telangana-500059. 2KP Labs, Kothapet, Hyderabad-500035 A B S T R A C T The Present work was to develop a simple, fast, accurate, precise, reproducible, Reverse Phase High Performance Liquid Chromatographic Method for simultaneous estimation of Valsartan and Sacubitril in ... Read More »

Analytical Method Development and Validation for Rabeprazole and Itopride in API and Combine Pharmaceutical Dosage Forms by RP-HPLC

Sanju Srinivas1, M. Suman2 1Associate Professor Department of Pharmacy, Ganga Pharmacy College, Nizamabad, Telangana 2Department of Pharmaceutical Analysis, Ganga Pharmacy College, Nizamabad, Telangana ABSTRACT A new method was established for simultaneous estimation of Rabeprazole and Itoprideby RP- HPLC method. The chromatographic conditions were successfully developed for the separation of Rabeprazole and Itopride by using Agilent C18 column (4.6×150mm) 5µ , ... Read More »

RP-HPLC Metthod Development and Vaidation for Velpatasvir and Voxilaprevir by Simulatneous Determination in Bulk and Their Pharamceutical Dosage Forms

MD. Abdul Sattar*, A. Suneetha Department of Pharmaceutical Analysis, Hindu college of Pharmacy, Amaravathi Road, Guntur-522002, A. P, India. A B S T R A C T Chromatography is the most powerful and versatile technique available to the modern analyst. In a single step process it can separate a mixture into its individual components and simultaneously provide a quantitative estimate ... Read More »

Development and Validation of a RP-HPLC Method for the Determination of Acyclovir in Transdermal Patches

R. Venu Priya1 and Vinesh Kumar2 1Research Scholar, Sun Rise University, Alwar, Rajasthan, India. 2Department of Pharmacy, Sun Rise University, Alwar, Rajasthan, India. A B S T R A C T The present report describes a rapid and sensitive High Pressure Liquid Chromatography (HPLC) method with UV detection to quantify acyclovir in transdermal patches. After sample preparation with diluent separation ... Read More »

Validation of Developed Analytical Method for Valsartan Floating Tablets by Reverse Phase High Performance Liquid Chromatography

C. Saravanan*1, M. Purushothaman2 1Sun Rise University, Alwar, Rajasthan – 301030, India 2Scient Institute of Pharmacy, Ibrahimpatnam, Ranga Reddy (Dt), Hyderabad, Talangana-501 506, India. A B S T R A C T Aim of the present investigation was to validate a new analytical, simple, sensitive, selective and precise High Performance Layer Chromatograpic (HPLC) method for the estimation of Valsartan in ... Read More »

Method Development and Validation of Omeprazole by RP-HPLC Method in Bulk and Its Pharmaceutical Dosage Form

Nagadani Kalyani*, R. Kiran Jyothi, Dr. K.B Chandra Sekhar Department of Pharmaceutical Analysis, JNTUA- Oil Technological and Pharmaceutical Research Institute, Ananthapuramu-515001, A. P, India A B S T R A C T Omeprazole is a proton pump inhibitor ﴾PPI﴿ and a potent inhibitor of gastric acidity which is mostly used in the therapy of gastroesophageal reflux and peptic ulcer disease. ... Read More »

A New Validated Stability Indicating RP-HPLC Method for the Simultaneous Estimation of Emtricitabine and Tenofovir Disoproxil Fumarate in Bulk Drug and Pharmaceutical Dosage Form

M. Bharathi*, P. Rameeja, V. Haribaskar, Ramesh Dhani, B. Swathi Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Muthukur, Nellore– 524 346 A B S T R A C T Simple precise and accurate method was developed for the estimation of Emtricitabine and Tenofovir disoproxil. The mobile phase consisting 80% buffer 20% Acetonitrile. The column was used Inertsil ODS ... Read More »

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