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 |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 422.46 kB | Adobe PDF | View/Open |
02_declaration.pdf | 304.34 kB | Adobe PDF | View/Open | |
03_certificates.pdf | 2.38 MB | Adobe PDF | View/Open | |
04_acknowledgement.pdf | 389.34 kB | Adobe PDF | View/Open | |
05_contents.pdf | 429.78 kB | Adobe PDF | View/Open | |
06_list of figure and table.pdf | 475.77 kB | Adobe PDF | View/Open | |
07_abstract.pdf | 424.55 kB | Adobe PDF | View/Open | |
08_ch 1 introduction.pdf | 735.28 kB | Adobe PDF | View/Open | |
09_ch 2 aim objective.pdf | 529.3 kB | Adobe PDF | View/Open | |
10_ch 3 liturature.pdf | 1.69 MB | Adobe PDF | View/Open | |
11_ch4 materials and methods.pdf | 831.13 kB | Adobe PDF | View/Open | |
12_ch5 result and discussion.pdf | 8.24 MB | Adobe PDF | View/Open | |
13_ch6 summary.pdf | 496.07 kB | Adobe PDF | View/Open | |
14_ch7 conculusion.pdf | 455.98 kB | Adobe PDF | View/Open | |
15_ch8 references.pdf | 615.6 kB | Adobe PDF | View/Open | |
16_list of publications.pdf | 550.94 kB | Adobe PDF | View/Open | |
17_plagiarism report.pdf | 1.12 MB | Adobe PDF | View/Open | |
80_recommendation.pdf | 919.33 kB | Adobe PDF | View/Open |
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