Paper Title
DEVELOPMENT AND VALIDATION OF EVOGLIPTIN IN BULK AND PHARMACEUTICAL DOSAGE FORM AND ITS STRESS DEGRADATION STUDIES
Article Identifiers
Authors
PAVAN SANJEEV DANGE , MONIKA P JADHAO
Keywords
Evogliptin, High Performance liquid Chromatography, Method Validation, Stability Indicating, Forced degradation study, ICH guidelines.
Abstract
A simple, rapid and precise reversed – phase High performance liquid chromatographic (RP-HPLC) stability indicating method was developed and validated for the determination of Evogliptin in the bulk and tablets. The method involves the use of commonly available and inexpensive laboratory reagents. Chromatographic separation of evogliptin was achieved using a reverse phase Zodiac C18 column (150mm × 4.6mm, 5µm) and Solvent A, 20mM KH2PO4 water-methanol (70:30%, v/v); Solvent B, acetonitrile-methanol (90:10, v/v) as mobile phase at 1.0 ml/min flow rate. Detection was carried out at 260 nm. Rt was found to be 3.463 min for Evogliptin tartrate in stability indicating method different stress conditions were applied.
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How To Cite (APA)
PAVAN SANJEEV DANGE & MONIKA P JADHAO (May-2023). DEVELOPMENT AND VALIDATION OF EVOGLIPTIN IN BULK AND PHARMACEUTICAL DOSAGE FORM AND ITS STRESS DEGRADATION STUDIES. INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 8(5), i780-i787. https://ijnrd.org/papers/IJNRD2305890.pdf
Issue
Volume 8 Issue 5, May-2023
Pages : i780-i787
Other Publication Details
Paper Reg. ID: IJNRD_197616
Published Paper Id: IJNRD2305890
Downloads: 000121994
Research Area: Pharmacy
Country: Buldana, Maharashtra, India
Published Paper PDF: https://ijnrd.org/papers/IJNRD2305890.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2305890
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Journal Name: INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT(IJNRD)
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This work is licensed under a Creative Commons Attribution 4.0 International License and The Open Definition
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