Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/397568
Title: A New RP_HPLC Method Development and Validation of Combination of Drugs and UPLC Separation Analysis of Amitripytline Pregabalin and Covid Drug Favipiravir
Researcher: SRIKANTH KANITHI
Guide(s): CH.N.S SAI PAVAN KUMAR
Keywords: Physical Sciences
Chemistry
Chemistry Medicinal
University: Vignans Foundation for Science Technology and Research
Completed Date: 2022
Abstract: An 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
Pagination: 183
URI: http://hdl.handle.net/10603/397568
Appears in Departments:Division of Chemistry

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1_title.pdf132.08 kBAdobe PDFView/Open
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8_chapter-1.pdf638.62 kBAdobe PDFView/Open
9_chapter-2.pdf543.72 kBAdobe PDFView/Open
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