A New RP_HPLC Method Development and Validation of Combination of Drugs and UPLC Separation Analysis of Amitripytline Pregabalin and Covid Drug Favipiravir

dc.contributor.guideCH.N.S SAI PAVAN KUMAR
dc.coverage.spatial
dc.creator.researcherSRIKANTH KANITHI
dc.date.accessioned2022-08-05T05:37:18Z
dc.date.available2022-08-05T05:37:18Z
dc.date.awarded
dc.date.completed2022
dc.date.registered2015
dc.description.abstractAn unpretentious, prompt, principled and obvious stability-indicating Ultra performance liquid chromatography (UPLC), High performance liquid chromatographic analytical approaches were industrialized and validated for the quantifiable analysis of dissimilar amalgamation of drugs. The amalgamation of drugs is sheltered COVID drug, Antidepressant drugs, HIV drugs and beta blocker drug with impurity contour. The drugs are Favipirivir/ Amitriptyline / Pregabalin, Emtricitabine / Tenofovir / Rilpivirine and Esmolol Hydrochloride bulk drug substance with ASL-8123 (Impurity A) and ACC-9675 (Impurity B) impurities. newlineThe amalgamation of COVID and antidepressant drugs technique was authenticated using Acquity UPLC-HSS, C18 (100 mm x 1.8µ) column and the column temperature was preserved at 25°C and run-time 3 minutes. The mobile phase was a combination of Mobile Phase: A Acetonitrile/Methanol, B 0.1% Ortho Phosphoric acid/TFA in water. The injection volume of examples was 1and#956;L. The amalgamation of HIV drugs technique was developed and validated with the column: C18 (250 mm x 4.6 mm, 5µ). The column temperature was continued at 25oC and run time 10 minutes. The mobile phase was a combination of Mobile Phase: A Acetonitrile, B 0.1% TEA in water (pH=3). The injection volume of tasters was 20and#956;L. UV detection was supported by using a UV-DAD detector at 265 nm. The beta blocker drug with impurities technique developed. validated, these impurities were acknowledged, and assemblies of impurities are established by NMR and spectroscopic studies (IR). Column used C8 (250 mm x 4.6 mm, 5µ). The column temperature was preserved at 30 oC and run-time 12 minutes. The mobile phase was a amalgamation of Mobile Phase: A Acetonitrile, B 0.01N Potassium dihydrogen ortho phosphate in water (pH=4.8). The injection volume of tasters was 10 and#956;L. UV detection was supported by using a UV-DAD detector at 221 nm.The validation of this technique was done as per ICH strategies. newline
dc.description.note
dc.format.accompanyingmaterialCD
dc.format.dimensions
dc.format.extent183
dc.identifier.urihttp://hdl.handle.net/10603/397568
dc.languageEnglish
dc.publisher.institutionDivision of Chemistry
dc.publisher.placeGuntur
dc.publisher.universityVignans Foundation for Science Technology and Research
dc.relation
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordPhysical Sciences
dc.subject.keywordChemistry
dc.subject.keywordChemistry Medicinal
dc.titleA New RP_HPLC Method Development and Validation of Combination of Drugs and UPLC Separation Analysis of Amitripytline Pregabalin and Covid Drug Favipiravir
dc.title.alternative
dc.type.degreePh.D.

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