Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/362477
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dc.date.accessioned2022-02-15T08:41:13Z-
dc.date.available2022-02-15T08:41:13Z-
dc.identifier.urihttp://hdl.handle.net/10603/362477-
dc.description.abstractThe cumulative objectives of present research work were as follows: newline1. To develop and validate accurate, precise, reproducible and reliable stability newlineindicating assay method. newline2. To perform stress degradation of some drugs with stability indicating assay method newlineas per ICH guidelines. newline3. To establish the structure of the degradants and degradation pathways of the drug newlinecandidates. newline4. To establish impurity profiling of some active pharmaceuticals (API) newlineFive APIs, viz. armodafinil (AMD), artemether (ART), olopatadine hydrochloride (OLO), newlineramelteon (RMT) and tapentadol hydrochloride (TAP) were used for the research work to newlineexplore the above objectives. newlineThe whole work was carried out on HPLC chromatograph model Agilent Infinity 1260 newlineseries equipped with 1260 binary pump VL 400 bar, 1260 manual injector 600 bar, newlineRheodyne 7725i 7-port sample injection valve with 20 and#956;L fixed loop, ZORBAX Eclipse newlinePlus C18 (250 × 4.6 mm, 5 and#61549;m), 1260 DAD VL, 20 Hz detector, standard flow cell 10 newlinemm, 13 and#61549;L, 120 bar, OpenLab CDS EZChrom Ed. Workstation and syringe 50.0 and#61549;L, FN, newlineLC tip. LC-MS was Micromass Q-TOF micro (Waters) equipped with separation module - newlineWaters Alliance 2795; LC column: Zorbax Eclipse Plus C18 column (250 × 4.6 mm, 5 newlineand#956;m); ionization - electro spray positive (ES+); acquisition: MRM (unit resolution). LC-MS newlinestudy was performed in positive mode using leucine enkephalin as standard. Ultraviolet newlinespectrophotometers (Shimadzu 1700 and 1800 series) with 1 cm matched quartz cells were newlineused for the present research work. newlineAs per ICH guidelines, developed methods for drugs were validated. The validated RPHPLC newlinemethods for APIs were successfully applied to establish degradation profiles and newlinestability indicating power of the method, as drugs were determined in presence of newlinedegradation products by their respective method. newline
dc.format.extent57.9MB
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleDegradation and Impurity Profiling of Some Active Pharmaceutical Ingredients
dc.title.alternative
dc.creator.researcherBASNIWAL, PAWAN KUMAR
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.description.note
dc.contributor.guideJAIN, DEEPTI
dc.publisher.placeBhopal
dc.publisher.universityRajiv Gandhi Proudyogiki Vishwavidyalaya
dc.publisher.institutionDepartment of Pharmacy
dc.date.registered2008
dc.date.completed2016
dc.date.awarded2016
dc.format.dimensionsA4
dc.format.accompanyingmaterialDVD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Pharmacy

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01_ title.pdfAttached File29.33 kBAdobe PDFView/Open
03_tables of contents.pdf28.76 kBAdobe PDFView/Open
04_list of table.pdf17.36 kBAdobe PDFView/Open
05_ list of figures.pdf28.91 kBAdobe PDFView/Open
06_acknowledgement.pdf15.91 kBAdobe PDFView/Open
07_ chapter 1.pdf35.03 kBAdobe PDFView/Open
08_chapter 2.pdf36.13 MBAdobe PDFView/Open
09_ chapter 3.pdf9.46 kBAdobe PDFView/Open
10_ a chapter 5.pdf11.21 MBAdobe PDFView/Open
10_ b chapter 6.pdf244.43 kBAdobe PDFView/Open
10_ chapter 4.pdf85.34 kBAdobe PDFView/Open
11_ refernces.pdf3.77 MBAdobe PDFView/Open
12_ publications.pdf7.22 MBAdobe PDFView/Open
80_recommendation.pdf49.77 kBAdobe PDFView/Open
abrreviation.pdf15.28 kBAdobe PDFView/Open
certificate.pdf174.18 kBAdobe PDFView/Open
declaration by the candidate.pdf213.84 kBAdobe PDFView/Open
preliminary page.pdf29.33 kBAdobe PDFView/Open


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