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Tag Archives: Pantoprazole

Development of Stability Indicating Assay Method for Antiemetic Drugs in Combined Dosage Formulation

A. Chavhan1, J.P. Ambhore2, S. A. Shinde3, A. N. Ugale4 1,2,3Dr. Rajendra Gode College of Pharmacy, Malkapur Dist- Buldana (MS) – 443101 4Government College of Pharmacy, Kathoranaka, Amravati Dist- Amaravati (MS)-444604 A  B  S  T  R A C T A new stability indicating reversed-phase high performance liquid chromatography method was developed for assay of Domperidone and Pantoprazolein tablet. The separation ... Read More »

Design and Development of Pantoprazole Floating In-Situ Gel

Bhargavi Tambali*, Venkata Ramana Bachu, Venkata Badarinath Atluri Dr. K. V. Subba Reddy Institute of Pharmacy, Kurnool, Andhra Pradesh, India – 518218 A B S T R A C T The aim of this investigation is to formulate and evaluate floating in- situ gel of Pantaprazole solution by using polymer dispersion technique. Pantoprazole is a proton pump inhibitor (PPI) that ... Read More »

Reverse Phase High Performance Liquid Chromatographic Technique for the Determination of Pantoprazole in Pure and Its Dosage Forms

Dr. Hareesh Dara, Meesa Rajendar, Dr. Ampati Srinivas St. John College of Pharmcy, Hasanparthy, Hanamkonda, Telangana, India 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 Pantoprazole, in its pure form as well as in tablet dosage form. Chromatography was carried out on ... Read More »

Analytical Method Development and Validation for the Estimation of Pantoprazole by RP-HPLC Method in Bulk and Pharmaceutical Dosage Form

Y. Krishna Reddy*, D. Ramesh, D. Kowshik, E. Manisha, K. Manisha, G. Kiranmayi    Bomma Institute of Pharmacy, Khammam, Telangana, India A B S T R A C T The chromatographic conditions were successfully developed for the separation of Pantoprazole by using thermosil C18 4.5×150 mm 5.0 µm, flow rate was 0.8ml/min, mobile phase ratio was 65:35% v/v methanol:water, detection ... Read More »

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