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Pavan Kumar.V*, P. Jyoshna, P. Nageena, E. Sandhya Mahalakshmi, K. Siva Kumar, A. Subha Jahnavi, A. Tharun Sai Department of Pharmaceutical Analysis, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati-517561 A B S T R A C T An elementary, valid, Speedy and decisive strategy was developed to determine Lisinopril and Amlodipine quantitatively in combined pharmaceutical dosage forms. The method was ... Read More »
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Method Development and Validation of Voglibose in Tablet Formulation by using UV Double Beam Spectrophotometer
K. Surendra*, S. Sreenivasulu, R. Srikanth, O. Kishore Chandra, A. Bhanu Prasad, Ch. Srinivasulu Rao’s College of Pharmacy, Chemudugunta, Venkatachalam, Nellore, Andhra Pradesh-524320 A B S T R A C T The present work was aimed to develop and validate UV spectrophotometric method for the quantification of Voglibose in tablet formulation. Distilled water used as a solvent. The absorption maxima ... Read More »
Method Development and Validation for the Assay of Nebivolol Tablets by using RP-HPLC
1N. Kalpana Devi*, 2Pradeep Reddy, 3D.S.S.N. Neelima 1,2 Teegala Krishna Reddy College of Pharmacy, Hyderabad, Telangana State 3 Vikas Institite of Pharmaceutical Sciences, Rajahmundary ABSTRACT A simple, precise, and accurate gradient reversed-phase (RP) high-performance liquid chromatographic (HPLC) assay method was developed and validated for determination of nebivolol in tablet dosage forms. gradient RP-HPLC separation was achieved on a Phenomenex, kinetex ... Read More »
Analytical Method Development and Validation for the Estimation of Ritonavir in Bulk and Pharmaceutical Dosage Form
K. Swapna1, M. Zaheer Ahamed1, M. Renamma1, B. Famida1, B. Mohammed Ishaq1*, Hindustan Abdul Ahad1, Ramesh Dhani2 1Department of Pharmaceutical Analysis, Balaji College of Pharmacy, Anantapur–515001, AP, India. 2Dept. of Pharmaceutical Chemistry, Ratnam Institute of Pharmacy, Nellore, Andhra Pradesh, India-524346 Received: 30 April 2014, Accepted: 6 June 2014, Published Online: 18 July 2014 Abstract A simple, robust, selective and sensitive ... Read More »
Development and validation of UV spectrophotometric method for the estimation of Zidovudine in bulk samples
R. Mounika1, B. Mohammed Ishaq1*, Hindustan Abdul Ahad1, B Faheem1, Ramesh Dhani2 1Department of Pharmaceutical Analysis, Balaji College of Pharmacy, Anantapur–515001, AP, India. 2Dept. of Pharmaceutical Chemistry, Ratnam Institute of Pharmacy, Nellore, Andhra Pradesh, India-524346 Received: 21 April 2014, Accepted: 28 May 2014, Published Online: 18 July 2014 Abstract A simple, sensitive, rapid and accurate UV spectroscopic method has been ... Read More »
Method development and validation for the simultaneous estimation of Nebivolol hydrochloride and S (-) Amlodipine besilate in tablet dosage form by RP – HPLC
About author Prabhakaran. V.*, Sekar. S., Baskar.E., Raghuprasath. V.R. Formulation Research and Development Department, The Madras Pharmaceuticals, Karapakkam, Chennai, Tamil Nadu, India. Email: [email protected] ABSTRACT High Performance Liquid Chromatography method was developed and validated in a simple, specific and precise manner for Nebivolol HCl and Amlodipine besilate in a combined solid dosage form. Nebivolol hydrochloride, a long acting, cardioselective β ... Read More »
