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Tag Archives: Validation

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 »

Method Development and Validation and Degradation Studies for Cinacalcet Hcl Drug by RP-HPLC Method

Eswara Rao Bammidi*1, Vaikuntarao Lakinani1, David Krupadanam Gazula Levi2 1Departmernt of Chemistry, GITAM Institute of Science, GITAM University, Visakhapatnam, A.P., India 2Department of Chemistry, Osmania University, Hyderabad. Received: 24 May 2014, Accepted: 26 June 2014, Published Online: 27 July 2014 Abstract The purpose of this study is to develop and validate a simple, rapid, sensitive, and precise, degradation studies for ... Read More »

Development and Validation of Simultaneous Determination of Vitamins B1, B2, B3, B6 and Folic Acid in Multivitamin Tablet by RP-HPLC

A. Sankara Avudaiappan1, A. Chenthilnathan1* and S. Vikraman2  1Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli – 627 012, Tamil Nadu, India. 2Apex Laboratories Private Limited, Alathur, Kancheepuram District-603110 Tamil Nadu, India. Received: 29 April 2014, Accepted: 15 June 2014, Published Online: 27 July 2014 Abstract A simple, efficient and reproducible RP-HPLC method for simultaneous determination of vitamins B1 (Thiamine mononitrate), ... Read More »

Development and Validation of Area under the Curve and first derivative methods for the Estimation of Levetiracetam in Bulk and Tablet Dosage Form by using UV Spectrophotometry

M. Lohita*, S. Shakirbasha, T. Edukondalu, S. Vijayaraj, P. Jayapreethi, K. Swetha  Department of Pharmacy, Sree Vidyanikethan College of Pharmacy, Sree sainath Nagar, A. Rangampet, Tirupathi–517102, Chitoor (Dt), Andhra Pradesh, India. Received: 15 May 2014, Accepted: 21 June 2014, Published Online: 18 July 2014 Abstract A simple, selective, precise and accurate ”AUC” and ”FIRST DERIVATIVE” methods for estimation of Levetiracetam drug ... Read More »

Method Development and Validation of Telmisartan in Bulk and Pharmaceutical Dosage Forms by UV Spectrophotometric Method

Author Details N. Samba Siva Naik*, G. Sai Phani, SD. Fathima Zahera, N. Sai Priyanka and CH. Ravi Tej Department of Pharmaceutical Analysis and Q.A, Narasaraopeta Institute of Pharmaceutical Sciences, Narasaraopeta Group of Institutions, Narasaraopet, Guntur (Dt.), Andhra Pradesh, India Abstract This research article describes the analytical method suitable for validation of Telmisartan by UV–spectro-photometric method. The method was utilized UV-Spectroscopy ... Read More »

Stability indicating High Performance Thin Layer Chromatographic determination of Raloxifene Hydrochloride

Author Details Rajasekaran A*, Preethi N, Arivukkarasu R  Department of Pharmaceutical Analysis, KMCH College of Pharmacy, Coimbatore, India Abstract A simple, sensitive, selective, precise and stability indicating high-performance thin-layer chromatographic method was developed and validated for the determination of raloxifene hydrochloride as per the ICH guidelines. Precoated aluminium plates with silica gel 60F254 as the stationary phase and methanol: water: ... Read More »

Validated RP-HPLC Method for Simultaneous Estimation of Lisinopril and Hydrochlorothiazide in Combined Dosage forms

Author Details P. Nagaraju*, G. Indira Priyadarshini, SA. Bilal Ahmed and V. Siddhartha Department of Pharmaceutical Analysis, Hindu College of Pharmacy, Amaravathi Road, Guntur–522 002, Andhra Pradesh, India. Abstract A rapid and sensitive reverse phase high performance liquid chromatography (RP-HPLC) method has been developed for simultaneous estimation of Lisinopril and Hydrochlorothiazide. Chromatographic separation was achieved on reverse phase Agilent LC 1100 ... Read More »

A Review on validation of Autoclave, Membrane Filtration

Author Details B. Venkateswara Reddy*, B. Rasmitha Reddy, K. Navaneetha St.pauls College of Pharmacy, Turkayamjal, R.R (Dist) -501510, Andhra Pradesh, India Abstract Validation is one of the important steps in achieving and maintaining the quality of the final product batch after batch. Without equipment, we cannot manufacture a product. If equipment is validated, we can ensure that our product is ... Read More »

Development and Validation of UV Spectrophotometric Method of Febuxostat in Bulk and Tablet Formulations

About author Raviteja, N. SambaSiva Naik*, Gayathri,  Sd.Fathima Zahera Narasaraopet Institute of Pharmaceutical Sciences, Narasaraopet, Andhra Pradesh, India E-mail: [email protected] Abstract The present research works discuss the development of a UV estimation method for febuxostat. Simple, fast, accurate and cost efficient and reproducible. Spectrophotometric method has been developed for the estimation of febuxostat in bulk and tablet formulations. The wave ... Read More »

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