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http://hdl.handle.net/10603/601175
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DC Field | Value | Language |
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dc.coverage.spatial | ||
dc.date.accessioned | 2024-11-14T06:42:44Z | - |
dc.date.available | 2024-11-14T06:42:44Z | - |
dc.identifier.uri | http://hdl.handle.net/10603/601175 | - |
dc.description.abstract | The intention and purpose of current research technique was into produce controlled (medicament) releasing formulations of drug Esomeprazole and drug Dexlansoprazole to increase bio-availability and prevent plasma variations associated into with existing innovator formulations. newline newlineIn third chapter an over all overview of concept is briefed. The concepted formulation as designed would increase in the time duration action while guaranteeing proper release, would standardize medication (drug) release, its kinetics, effectively this can minimize dose (sudden) dumping, consequently it releases the API drug away from formulation at a predetermined pace of (molecule) drug liberation, locally or in systemic area and eventually reduce variation of the steady-state level. This in turn would enhance patient convenience, enhance safety, improve the health condition of the patient and increase therapeutic pharmacological efficacy. The third chapter also describes the taken overall course for the entire work. newline newlineIn fourth chapter the methodology of experiments was described. Esomeprazole[API] and Dexlansoprazole were procured from different pharmaceutical companies in Bangalore and Mumbai, respectively. Esomeprazole is (an API) drug that is a proton (H+) pump - inhibitor, that lessens the acid in stomach production by block and prevent the proton (H+) pump as this is final step, of stomach for acid (H+) production. Dexlansoprazole, is another proton (H+) pump - inhibitor that can selectively inhibit the (H+), K+)-ATPase on the secretory membrane of stomach parietal cells. Polymer like the Eudragit®- S 100, Eudragit®- L 100, Eudragit®- RS PO, and Eudragit®- RL PO obtained from very reliable and authentic sources. Similarly, all other polymers were like Carbopol®-974 P, Pectin, newline newline | |
dc.format.extent | ||
dc.language | English | |
dc.relation | ||
dc.rights | self | |
dc.title | Formulations for Monitored Administration of Proton Pump Inhibitors | |
dc.title.alternative | FORMULATIONS FOR MONITORED ADMINISTRATION OF PROTON PUMP INHIBITORS | |
dc.creator.researcher | Shashi Shekhar Tripathi | |
dc.subject.keyword | Clinical Pre Clinical and Health | |
dc.subject.keyword | Pharmacology and Pharmacy | |
dc.subject.keyword | Pharmacology and Toxicology | |
dc.subject.keyword | Pharmacy | |
dc.description.note | ||
dc.contributor.guide | A. K. S. RAWAT | |
dc.publisher.place | Lucknow | |
dc.publisher.university | Maharishi University of Information Technology | |
dc.publisher.institution | Department of Pharamaceutical Sciences | |
dc.date.registered | 2020 | |
dc.date.completed | 2024 | |
dc.date.awarded | 2024 | |
dc.format.dimensions | ||
dc.format.accompanyingmaterial | DVD | |
dc.source.university | University | |
dc.type.degree | Ph.D. | |
Appears in Departments: | Department of Pharamaceutical Sciences |
Files in This Item:
File | Description | Size | Format | |
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1. title.pdf | Attached File | 205.89 kB | Adobe PDF | View/Open |
2_merged.pdf | 1.59 MB | Adobe PDF | View/Open | |
80_recommendation.pdf | 460.88 kB | Adobe PDF | View/Open | |
abstract.pdf | 105.36 kB | Adobe PDF | View/Open | |
chapter 1.pdf | 469.32 kB | Adobe PDF | View/Open | |
chapter 2.pdf | 273.49 kB | Adobe PDF | View/Open | |
chapter 3.pdf | 310.28 kB | Adobe PDF | View/Open | |
chapter 4.pdf | 1.69 MB | Adobe PDF | View/Open | |
chapter 5.pdf | 3.53 MB | Adobe PDF | View/Open | |
chapter 6.pdf | 298.42 kB | Adobe PDF | View/Open | |
contents.pdf | 284.14 kB | Adobe PDF | View/Open | |
references_merged.pdf | 2.46 MB | Adobe PDF | View/Open |
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