Friday , 27 November 2020

Tag Archives: RP-HPLC

Analytical Method Development and Validation by RP-HPLC for Simultaneous Estimation of Esomeprazole and Levosulpiride in Combined Capsule Dosage Form

V. Amaravathi*, Ramesh Dhani, V. Haribaskar, M. Gobinath, M. Shirisha Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Muthukur, SPSR Nellore, A.P, India A B S T R A C T A simple, Accurate, precise method was developed for the simultaneous estimation of the esomeprazole and levosulpiride in Capsule dosage form. Chromatogram was run through ODS (150mm 4.6mm, 5µ). ... Read More »

Method Development and Validation for Simultaneous Estimation of Propranolol and Valsartan by using RP-HPLC in Bulk and Pharmaceutical Dosage Form.

V. Bhargavi2, P. Sowjanya3, Dr. T. Rajesh4, Dr. Gampa Vijaya Kumar*1 1Professor and Head, Dept. of Pharmacy, KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy. 2,3,4Deapartment of Pharmacy, KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy. A B S T R A C T A simple, sensitive and precise reverse phase high performance liquid chromatographic method has been ... Read More »

Method Development and Validation for Simultaneous Determination a Multiple Drug Dosage Form of Paracetamol, Phenylepherine and Caffeine by RP-HPLC

Dr. Samson Israel Deta*1, Dr. Kommana Balaram Kumar2, Hayelom G/Kirstos Mangesha3 1Asst. Prof, Adigrat University, Ethiopia 2Asst.Prof, University of Gondar, Ethiopia 3Lecturer, Adigrat University, Ethiopia A B S T R A C T This method describes a procedure to quantify the assay of Paracetamol, Phenylepherine and caffeine tablet using a mobile phase containing containing mixture of 880 mL of sodium ... Read More »

Method Development and Validation of Valacyclovir in Pharmaceutical dosage form by RP-HPLC Method

Pavan Kumar V*1, Dr. C. Sreedhar1, Pavan Kumar Sai.B2, Haritha.Y3, Manisha.N4, Venkateswarlu G4 1Department of Pharmaceutical Analysis, Karnataka College of Pharmacy, Bengaluru, Karnataka 2Department of Pharmaceutical Analysis & Quality Control, Alliance Institute of Advanced Pharmaceutical and Health Sciences, Hyderabad, Telangana. 3Department of Pharmaceutics, Gokula Krishna College of Pharmacy, Sullurpet, Nellore (DT), Andhra Pradesh. 4Aurobindo Pharma Limited, Hyderabad, Telangana, India A ... Read More »

Analytical Method Development and Validation of Simultaneous Estimation of Tramadol, Paracetamol, Domperidone in Tablet Dosage Form by RP-HPLC

Nagaraju.Y*, A. Ajitha and Uma Maheshwar Rao. V Departmentof Pharmaceutical Analysis, CMR College of Pharmacy, Ranga Reddy-501401, India A B S T R A C T A simple reverse phase high pressure liquid chromatography (RP-HPLC) method has been developed and validated for simultaneous estimation of tramadol paracetamol and domperidone in tablet dosage forms. The compounds were separated on inertsil C-18 ... Read More »

Method Development and Validation of Nebivolol by RP-HPLC

Naga Jyothi. C*, Gummi Vishwanth, P. Sunitha Pharmaceutical Analysis and Quality Assurance,   JNTUH, Kukutpally, Hyderabad, India A B S T R A C T An isocratic reversed-phase high performance liquid chromatographic method was established for the estimation of Nebivolol in tablet dosage form. The chromatographic conditions were successfully developed for the estimation of Nebivolol by using Develosil C18 column (150×4.6mm, ... Read More »

Analytical Method Development and Validation for Simultaneous Estimation of Ambroxol HCL and Levocetrizine in Its Bulk and Dosage Form by RP-HPLC

R. Vivek*, Dr. T. Rama Mohan Reddy, Dr. V. Uma Maheswara Rao Department of Pharmaceutical Analysis and Quality Assurance, CMR College of Pharmacy, Medchal, Hyderabad, Rangareddy, India A B S T R A C T A simple Reverse phase liquid chromatographic method has been developed and subsequently validated for simultaneous determination of Levocetirizine and Ambroxol HCl in combination. The separation ... Read More »

Analytical Method Development and Validation for Simultaneous Estimation of Albendazole and Ivermectin Tablet of Dosage Form by RP-HPLC

B. Saidulu*, G. Usha Sree, Dr. V. Uma Maheswara Rao Department of Pharmaceutical Analysis and Quality Assurance, CMR College of Pharmacy, Medchal, Hyderabad, Rangareddy, India A B S T R A C T A reverse phased liquid chromatography (LC) method was developed and validated for simultaneous estimation of albendazole and ivermectin in tablet dosage form. The isocratic LC analysis was ... Read More »

Development and Validation of RP-HPLC Method for the Quantitative Determination of Fexofenadine Hydrochloride in Tablet Dosage form

P. Rajamathi1, A. Chenthilnathan1* and A. Sathish babu2 1Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli–627 012, Tamil Nadu, India. 2The Madras Pharmaceuticals, Chennai – 600 096, Tamil Nadu, India. Abstract Fexofenadine hydrochloride is a non-sedative and selective peripheral H1 receptor antagonist used for allergic rhinitis and chronic urticaria. This paper deals with a simple, feasible and sensitive reverse-phase high-performance liquid ... Read More »

A Novel validated RP-HPLC method for the estimation of “Rupatadine” in its Bulk and Pharmaceutical Dosage forms

CH. Naveen Kumar*, Arvapalli Rajani, Vemula Madhavi Latha, Vijaya Kuchana Department of Pharmaceutical Analysis and Quality Assurance, Teegala Krishna Reddy College of Pharmacy, Hyderabad, India Abstract A Novel Reverse Phase High Performance Liquid Chromatography (RP-HPLC) method for the Estimation of “Rupatadine” has been developed. The developed method was found and proved to be a better one than the already existing ... Read More »

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