Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/585256
Title: analysis of some anti diabetic agents in bulk and their synthetic mixture by chromatographic methods
Researcher: DESAI, SALONI ASHOKBHAI
Guide(s): Mardia, Rajnikant
Keywords: Clinical Pre Clinical and Health
Pharmacology and Pharmacy
Pharmacology and Toxicology
University: Dharmsinh Desai University
Completed Date: 2024
Abstract: RP-HPLC: The degradation study revealed that MET, SAXA, and DAPA followed first-order kinetics in all stress conditions as all the Log concentration vs. time graphs were linear with a regression coefficient near 1. With the increase in 20-degree temperature, the reaction rate increased by almost two folds, and the rate constant increased. As per the Arrhenius equation, ln k is inversely proportional to temperature., which was demonstrated experimentally that the value of the constant increased with an increase in temperature. All three drugs were more liable to oxidative conditions while showing good photolytic study stability. HPTLC: MET showed slower degradation than DAPA and SAXA in both acidic and basic conditions. The proposed method is precise, and the percentage relative standard deviation was between 0.5 and 2.0. The observed percentage recoveries were between 96.7 and 99.54 for all three compounds. The results from the degradation study stipulated that on exposure to various stressors, namely acid, alkali, oxidative, and UV light, the MET, DAPA, and SAXA. t-test was applied to compare the results of % Recovery for pure drugs. The results of and t-test revealed that calculated T values were less than the tabulated values, stating no significant difference between the two methods, indicating that the proposed RP-HPLC and LC-MS/MS appear to be equally suiTable for routine determination of ALO and PIO simultaneously in formulations. newline
Pagination: 337
URI: http://hdl.handle.net/10603/585256
Appears in Departments:Pharmacy

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02_prelim pages.pdf279 kBAdobe PDFView/Open
03_content.pdf554.63 kBAdobe PDFView/Open
04_abstract.pdf162.14 kBAdobe PDFView/Open
05_chapter 1.pdf442.33 kBAdobe PDFView/Open
06_chapter 2.pdf696.96 kBAdobe PDFView/Open
07_chapter 3.pdf77.77 kBAdobe PDFView/Open
08_chapter 4.pdf671.34 kBAdobe PDFView/Open
09_chapter 5.pdf6.71 MBAdobe PDFView/Open
10_annexures.pdf1.55 MBAdobe PDFView/Open
11_chapter 6.pdf3.75 MBAdobe PDFView/Open
12_chapter 7.pdf482.23 kBAdobe PDFView/Open
13_chapter 8.pdf272.85 kBAdobe PDFView/Open
14_references.pdf232.42 kBAdobe PDFView/Open
80_recommendation.pdf65.58 kBAdobe PDFView/Open
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