Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/404981
Title: Comparison of Microwave Assisted and Conventional Degradation of Drugs
Researcher: Tailor Pratik MehulKumar
Guide(s): Shah Shailesh A
Keywords: Drug analysis
Pharmacy
Quality Assurance
University: Uka Tarsadia University
Completed Date: 2022
Abstract: The drug development life cycle is a time-consuming process, which also involves lots of effort in the testing of the chemical stability of the drug molecules and possible impurity and degradation product of the drug before it comes in the form of a stable formulation. The Forced degradation and stability testing involve the major time portion in researching the chemistry of the molecules. To get a green and rapid method for forced degradation study of the drug molecules, the selected drug molecules were degraded using a microwave-assisted forced degradation process. Microwave-assisted degradation, being a different mechanism, is compared with the forced degradation process in conventional mode. newlineDrugs from the cardio diabetic category Sitagliptin, Linagliptin, Nifedipine, Cilnidipine, Canagliflozin, Telmisartan, and Rosuvastatin were selected. The hydrolytic degradation of drugs was performed in acid, alkaline, and neutral media. The preliminary degradation was performed at microwave power level 400 Watts for 2 min and 80 ° C for 2 hours. The results of the degradation were compared using validated chromatographic methods. The number of peaks and pattern of degradation were observed. After having data from the preliminary degradation study suitable degradation conditions were selected for the kinetics study. It was performed for each drug to get insight into the rate of degradation. The microwave-assisted degradation appears to be eight to ten times faster than conventional degradation. The microwave-assisted degradation gives the same results as that of conventional so it can be further used for stability-indicating method development and impurity analysis for drug substances. newline newline newline
Pagination: xxiv;211p
URI: http://hdl.handle.net/10603/404981
Appears in Departments:Faculty of Pharmacy

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01_title.pdfAttached File422.46 kBAdobe PDFView/Open
02_declaration.pdf304.34 kBAdobe PDFView/Open
03_certificates.pdf2.38 MBAdobe PDFView/Open
04_acknowledgement.pdf389.34 kBAdobe PDFView/Open
05_contents.pdf429.78 kBAdobe PDFView/Open
06_list of figure and table.pdf475.77 kBAdobe PDFView/Open
07_abstract.pdf424.55 kBAdobe PDFView/Open
08_ch 1 introduction.pdf735.28 kBAdobe PDFView/Open
09_ch 2 aim objective.pdf529.3 kBAdobe PDFView/Open
10_ch 3 liturature.pdf1.69 MBAdobe PDFView/Open
11_ch4 materials and methods.pdf831.13 kBAdobe PDFView/Open
12_ch5 result and discussion.pdf8.24 MBAdobe PDFView/Open
13_ch6 summary.pdf496.07 kBAdobe PDFView/Open
14_ch7 conculusion.pdf455.98 kBAdobe PDFView/Open
15_ch8 references.pdf615.6 kBAdobe PDFView/Open
16_list of publications.pdf550.94 kBAdobe PDFView/Open
17_plagiarism report.pdf1.12 MBAdobe PDFView/Open
80_recommendation.pdf919.33 kBAdobe PDFView/Open
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