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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/14972
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dc.contributor.authorSidhu, Jagpreet Singh-
dc.date.accessioned2024-05-22T09:43:37Z-
dc.date.available2024-05-22T09:43:37Z-
dc.date.issued2019-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2019/ay/c9ay01464k-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14972-
dc.description.abstractUric acid is an important inflammatory component, which is produced by the xanthine oxidase (XO)-catalyzed reaction of xanthine. The presence of uric acid in blood serum above the normal value leads to the formation of urate crystals and causes the growth of gout. Therefore, herein, a naphthalimide-based turn-on fluorescent probe was developed to monitor the uric acid and xanthine oxidase concentration in an aqueous system. The probe exhibited high selectivity towards uric acid and the xanthine oxidase-catalyzed reaction of xanthine. The fluorescence emission of the probe was enhanced upon the binding of uric acid, generated by the XO-assisted oxidation reaction. The detection limit for xanthine oxidase was calculated to be 0.7 U mL−1. The specificity of the probe for xanthine oxidase was confirmed by treating the enzyme with allopurinol. The endogenous images of uric acid in HeLa cells were obtained using a fluorescence microscope.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectPharmacyen_US
dc.subjectUric aciden_US
dc.subjectNaphthalimide-baseden_US
dc.subjectXanthine oxidaseen_US
dc.titleA naphthalimide-based novel “Turn-On” fluorescence approach for the determination of uric acid and monitoring of xanthine oxidase activityen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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