Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/54472
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dc.contributor.authorChen, Yahong-
dc.contributor.authorChang, Weixiao-
dc.contributor.authorZhu, Xue-
dc.contributor.authorWang, Ruiyong-
dc.contributor.authorTian, Fengshou-
dc.date.accessioned2020-06-05T07:34:03Z-
dc.date.available2020-06-05T07:34:03Z-
dc.date.issued2020-06-
dc.identifier.issn0975-0959 (Online); 0301-1208 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/54472-
dc.description270-276en_US
dc.description.abstractThe mechanism of fluorescence quenching of the product S in the presence of captopril was studied. The maximum emission wavelength of the product S was at 405 nm with the excitation wavelength at 316 nm. It was found that the fluorescence quenching of product S was of a static one and the binding constant (K) was 9.29 × 106 J mol-1. A linear relationship was found between the relative fluorescence intensity of the product S-captopril system and the concentration of captopril. Under optimum conditions, the linear range of the calibration curve for captopril was 2~160 μg L-1 with a correlation coefficient of 0.9926 and a detection limit of 0.1 μg L-1. The relative standard deviation (RSD) was 3.60%. The analytical results of the pharmaceuticals obtained by this novel method agreed quite well with those obtained by the KIO3 titrimetry.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBB Vol.57(3) [June 2020]en_US
dc.subjectCaptoprilen_US
dc.subjectEnzyme-catalyzed producten_US
dc.subjectFluorescence quenchingen_US
dc.titleFluorescence quenching and measurement of captopril in pharmaceuticalsen_US
dc.typeArticleen_US
Appears in Collections:IJBB Vol.57(3) [June 2020]

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