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UV Spectroscopy Assay Method Development and Validation of Dimethyl Fumarate and Cyclosporine Drugs in Nano Dosage Forms

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dc.contributor.author Patel, Sneha
dc.contributor.author Pathak, Drashti
dc.contributor.author Patel, Deepa
dc.date.accessioned 2020-11-24T03:50:59Z
dc.date.available 2020-11-24T03:50:59Z
dc.date.issued 2020-03
dc.identifier.issn 0975-9506
dc.identifier.uri http://ir.paruluniversity.ac.in:8080/xmlui/handle/123456789/7913
dc.description.abstract An easy, precise and accurate spectroscopic technique for the estimation of cyclosporine and dimethylfumarate in pure form and nano dosage form has been developed. The proposed method involves dissolving dimethylfumarate in distilled water and cyclosporine in ethanol and subjecting resulting solution to UV spectroscopic assessment. Absorption maximum was found 210 and 214 nm respectively. Beer’s law was obeyed in the concentration range of 1 to 5and 1 to 8 μg/mL for dimethylfumarate and cyclosporine. Calibration curve showd linearity between absorbance and concentration as per line equation with R2 value near 1. Validation was performed as ICH guildelines for linearity, accuracy, precision, Robustness, System suitability. en_US
dc.language.iso en en_US
dc.publisher International Journal of Pharmaceutical Quality Assurance | Volume-11 | Issue-1 en_US
dc.subject Cyclosporine, Dimethyl fumarate, Spectrophotometry, Validation en_US
dc.title UV Spectroscopy Assay Method Development and Validation of Dimethyl Fumarate and Cyclosporine Drugs in Nano Dosage Forms en_US
dc.type Article en_US


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