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Rapid and accurate HPLC method has been developed for the simultaneous estimation of Linagliptin and Lobeglitazone in tablet dosage form. Chromatographic separation of both anti-diabetic drugs was achieved on a Hypersil BDS C18 column (250 mm × 4.6 mm, 5 µm) using a mobile phase consisting of 760 mL methanol and 240 mL of buffer (0.2% FTA in water), at a flow rate of 1.0 mL/min. Detection was carried out at 275 nm. The separation was achieved in less than 10 minutes. The method was validated as per ICH guidelines for parameters including linearity, accuracy, precision, system suitability, specificity, robustness, limit of detection (LOD), limit of quantitation (LOQ), and range. Linearity, accuracy, and precision were found to be within acceptable limits over the range of 0.5–3.0 µg/mL for Lobeglitazone and 5–30 µg/mL for Linagliptin. The method proved to be sensitive, specific, and suitable for routine quality control of these drugs in pharmaceutical formulations.
"Formulation Analytical Method Development And Validation of Anti- Diabetic Drugs", International Journal for Research Trends and Innovation (www.ijrti.org), ISSN:2455-2631, Vol.10, Issue 6, page no.b479-b485, June-2025, Available :http://www.ijrti.org/papers/IJRTI2506156.pdf
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2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator