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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 ... Read More »
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Tag Archives: Validation
Method Development and Validation of Brinzolamide and Brimonidine In Its Bulk And Ophthalmic Dosage Form By Using RP-HPLC
Dr. K. Nageswara Rao1*, Raghava Doonaboyina2, R.Hema3 1Professor and Head, Department of Pharmaceutical Analysis, K.G.R.L College of Pharmacy, KGRL Road, Bhimavaram, West Godavari, Andhra Pradesh, India. 2Associate Professor and Head, Department of Pharmaceutical Chemistry, K.G.R.L College of Pharmacy, KGRL Road, Bhimavaram, West Godavari, Andhra Pradesh, India. 3K.G.R.L College of Pharmacy, KGRL Road, Bhimavaram, West Godavari, Andhra Pradesh, India. A B ... Read More »
Validation of HPLC Method of Aceclofenac and Rabeprazole Sodiumin Aceclofenac Sustained Release and Enteric Coatedrabeprazole Sodium Capsules
Kalpana Patankar-Jain1, Parag Gadkari2, Pushkar Pradhan3 1Department of Chemistry, B. N. N. College, Bhiwandi 2Inventia Healthcare Pvt. Ltd., Thane 3Department of Chemistry, Ramnarain Ruia College, Mumbai A B S T R A C T The current research paper gives method validation report for the simultaneous quantification of Aceclofenac Sustained Release 200mg and Enteric Coated Rabeprazole 20mg capsules. The method involved ... Read More »
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 »
