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Tag Archives: Validation

Stability Indicating RP-HPLC Method for Simultaneous Estimation of Lumacaftor and Ivacaftor in Bulk and Pharmaceutical Dosage Forms

Rameeja Pattan*, V. Haribaskar, Pasala Sandhya Mounika, Ramesh Dhani, B. Prathap Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Muthukur, Nellore A B S T R A C T A simple, fast, accurate, precise, reproducible Stability indicating Reverse phase High performance liquid chromatography (RP-HPLC) method was developed and validated for the determination of Lumacaftor and Ivacaftor in Bulk and ... Read More »

Simultaneous Estimation Method Development and Validated on Timolol Maleate and Brimonidine Tartrate by Using HPLC

1N.Kalpana Devi*, 2Sindhu Priya Mattepalli, 3D.S.S.N. Neelima 1,2 Teegala Krishna Reddy College of Pharmacy, Hyderabad Telangana State 3Vikas Institite of Pharmaceutical Sciences – Rajahmundary ABSTRACT A rapid and precise reverse phase high performance liquid chromatographic method has been developed for the validated of Timolol Maleate and Brimonidine Tartrate, in its pure form as well as in tablet dosage form. Chromatography was carried out ... Read More »

Analytical Method Development and Validation for Metoclopramide Hydrochloride by Using RP-HPLC

Meghnath chaudhary*, Dr. C. Sreedhar, T. Sreenivasarao, Katikala Dharmendra Department of Pharmaceutical analysis, Karnataka College of Pharmacy, 33/2, Thirumenahalli, Hegde Nagar Main Road, Jakkur Post, Bengaluru, Karnataka 560064 Abstract A simple, rapid, and sensitive high-performance liquid chromatographic method was developed and validated for determination of Metoclopramide Hydrochloride. Separation of Metoclopramide Hydrochloride was achieved within a single chromatographic run on an ... Read More »

Stability Indicating RP-HPLC Method for Simultaneous Estimation of Lumacaftor and Ivacaftor in Bulk and Pharmaceutical Dosage Forms

Pasala Sandhya Mounika, Rameeja Pattan* Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Muthukur, Nellore ABSTRACT A simple, fast, accurate, precise, reproducible Stability indicating Reverse phase High performance liquid chromatography (RP-HPLC) method was developed and validated for the determination of Lumacaftor and Ivacaftor in Bulk and pharmaceutical dosage form. Chromatographic separation was  done  by using Agilent Eclipse XDB-C8 column ... Read More »

Stability Indicating RP-HPLC Method for Simultaneous Estimation of Sofosbuvir and Velpatasvir in Bulk and Pharmaceutical Dosage Form

V. Hari Baskar, Ramesh Dhani*, P. Priyanka, M. Suchitra Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Nellore. ABSTRACT A simple, precise, accurate rp-hplc method has been developed and validated for the sofosbuvir and velpatasvir in bulk and pharmaceutical dosage form. This method was carried out by using Inertsil ODS-3(4.6 x 150mm, 5mm).  Mobile phase containing phosphate buffer (ph4.8): ... Read More »

RP-HPLC Method Development and Validation for Simultaneous Estimation of Bupropion and Naltrexone in Bulk and Pharmaceutical Dosage Forms

Sanju Srinivas and V. Nirmala* Associate Professor Department of Pharmacy, Ganga Pharmacy College, Nizamabad, Telangana *Department of Pharmaceutical Analysis, Ganga Pharmacy College, Nizamabad, Telangana A B S T R A C T Thus the proposed stability indicating RP-HPLC technique for the synchronic determination of Naltraxone and Bupropione in bulk and pharmaceutical dosage form was accurate, precise, linear, reliable, simple, economic ... Read More »

Analytical Method Development and Validation for the Simultaneous Estimation of Celecoxib and Diacerein in Bulk and Pharmaceutical Dosage Form Using RP-HPLC

Ameena Parveen1*, Dr. R. Vani2, Dr. M. Sunitha 1Post-graduate student, Shadan Women’s College of Pharmacy, Hyderabad, India 2Head of the department, Pharmaceutical Analysis, Shadan Women’s College of Pharmacy, Hyderabad 3Principal, Shadan Women’s College of Pharmacy, Hyderabad, India A B S T R A C T A new simple, accurate, precise and reproducible RP-HPLC method has been developed for the simultaneous ... Read More »

Reverse Phase High Performance Liquid Chromatographic Technique for the Determination of Rabeprazole in Pure and It’s Dosage Form

Dr. Hareesh Dara*, Meesa Rajendar St John College of Pharmcy, Hasanparthy, Hanamkonda, Telangana. 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 Rabeprazole, in its pure form as well as in tablet dosage form. Chromatography was carried out on a Symmetry C18 (4.6 ... Read More »

Method Development and Validation for the Quantitative Estimation of Citalopram in Bulk and Pharmaceutical Tablets by RP-HPLC

Bushra Nazeer and P. Bharath Rathna Kumar* Department of Pharmaceutical Analysis & Quality Assurance, Anwarul Uloom College of Pharmacy, New Mallepally, Hyderabad, Telangana, India. A B S T R A C T In this study, a simple, precise and accurate reverse phase high performance liquid chromatography was developed for the estimation of citalopram in bulk and pharmaceutical dosage forms. A ... Read More »

Review on Bioanalytical Method Development and Validation

Dr M.sunitha1*, Nabila Quddus2, Naila Sadiq3, Dr R. Vani4* 1Principal, Shadan Women’s College of Pharmacy, Hyderabad, India 2Post graduate student, Shadan Women’s College of Pharmacy, Hyderabad, India 3Post graduate student, Shadan Women’s College of Pharmacy, Hyderabad, India 4Head of the department, Pharmaceutical Analysis, Shadan Women’s College Of Pharmacy, Hyderabad, India ABSTRACT Bioanalytical methods are used for the quantitative analysis of ... Read More »

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