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Rajkiran Kolakota*, Y. Rupavathi Department of Pharmaceutical Analysis, Sri Sivani College of Pharmacy, NH-16, Chilakapalem Jn, Srikakulam-532402, A.P ABSTRACT A HPLC method was developed and validated to determine trace amounts of levofloxacin related substances & degradation products in its formulation. Separation of levofloxacin from impurity A, impurity B, impurity C and unknown degradation products was achieved on a YMC-Pack Pro ... Read More »
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HPLC Estimation of Paroxetine in Bulk and Pharmaceutical Formulations
Rajkiran Kolakota*, P. Anil Naidu, Uha Rani Duppala Department of Pharmaceutical Analysis, Sri Sivani College of Pharmacy, NH-16, Chilakapalem Jn, Srikakulam-532402, AP A B S T R A C T A simple and reproducible method was developed for Paroxetine by Reverse Phase High Performance Liquid Chromatography (RP-HPLC). Paroxetine was separated on ODS column (150 x 4.6 mm, 5μm), using Phosphate ... Read More »
Modernization of Medical Devices and Market-Oriented Economies in United Kingdom
Rajkiran Kolakota*, D. Usharani Department of Pharmaceutical Regulatory Affairs, Sri Sivani College of Pharmacy, NH-16, Chilakapalem Jn, Srikakulam-532402, A.P A B S T R A C T The purpose of this study is to illuminate the importance of medical devices, regulatory requirements for the registration of medical device manufacturers in U.K. The controversy for companies developing and producing medical device ... Read More »
A new RP-HPLC method development and validation for Simultaneous estimation of lumefantrine & artemether using bulk and Pharmaceutical Dosage Forms
Rajkiran Kolakota*, G. Sai Krishna Department of Pharmaceutical Analysis, Sri Sivani College of Pharmacy, NH-16, Chilakapalem Jn, Srikakulam-532402, A.P. A B S T R A C T A simple, rapid, accurate and precise isocratic reversed phase high performance liquid chromatographic method has been developed and validated for Simultaneous Estimation of Lumefantrine and Artemether in Combined Dosage Form. The chromatographic separation ... Read More »
An Insight of Microsponges for Acne Treatment
Vinay Richards R 1*, Dr. Bhuwanendra Singh2 1Research Scholar, Department of Pharmaceutical Sciences, Shri Venkateswara University, Venkateshwara Nagar, Rajabpur Gajraula, Amroha, UP-244236. 2Research Supervisor, Department of Pharmaceutical Sciences, Shri Venkateswara University, Venkateshwara Nagar, Rajabpur Gajraula, Amroha, UP-244236. A B S T R A C T Dermatological disorders have a significant psychosocial impact, impairing the patient’s life significantly. Topical therapy is ... Read More »
Study Process of Drug Approval Process in European Union via Centralized Procedure (From 2015-2018)
Rajkiran Kolakota*, I. Uma Department of Pharmaceutical Regulatory Affairs, Sri Sivani College of Pharmacy, NH-16, Chilakapalem Jn, Srikakulam-532402, AP. A B S T R A C T The current scenario of this article mainly highlights about the medicinal products that are highly synchronized in European Union. Medicinal products undergo an elaborate system of approvals that governs how, when, where, and ... Read More »
A New RP-HPLC method developed and validated for the estimation of Tolterodine
Gobalakrishnan P*1, Munisekhar V, Hemanth Kumar V 1Department of Pharmaceutical Analysis, Vagdevi College of Pharmacy & Research Centre, Nellore, Andhra Pradesh, India. A B S T R A C T A rapid and sensitive RP-HPLC Method with UV detection (283nm) for routine analysis of Tolterodine in Bulk and in Pharmaceutical formulation was developed. Chromatography was performed with mobile phase containing ... Read More »
Analytical Method Development and Validation of Hydrochlorothiazide and Eposartan in API and its Dosage form by RP-HPLC
R. Narsimha Rao1, N. Karnakar2 J. Sushma3, P. Amani4 1,2,3,4Venkateshwara Institute of Pharmaceutical Sciences, Charlapally, Nalgonda, Telangana. A B S T R A C T On the basis of experimental results, the proposed method is suitable for the quantitative determination of Hydrochlorothiazide and Eposartan in pharmaceutical dosage form. The method provides great sensitivity, adequate linearity and repeatability. The estimation of ... Read More »
Regulatory Approval Procedures in USA
J. Praveen Kumar1, Rajendran Sai Divya2, Dr. M. Kishore Babu3, Dr. P.V. Murali Krishna4 1Associate Professor, Krishna Teja Pharmacy College, Tirupati, Andhra Pradesh. 2Krishna Teja Pharmacy College, Tirupati, Andhra Pradesh. 3Principal, Krishna Teja Pharmacy College, Tirupati, Andhra Pradesh. 4Associate professor, MNR College of Pharmacy, Sangareddy, Hyderabad, Telangana. A B S T R A C T The Food and Drug Administration ... Read More »
Preparation and Evaluation of Solid dispersions of Febuxostat
Radhika P*, Venkata Ramana M1 *Moonray College of Pharmacy, Hyderabad, Telangana. 1Azad College of Pharmacy, Hyderabad, Telangana A B S T R A C T Among the various methods of enhancement of dissolution rate and oral bioavailability, cyclodextrin complexation and solid dispersion technologies were found to be very successful with Febuxostat. As such their oral bioavailability and efficacy are severely ... Read More »
