Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1734
DC FieldValueLanguage
dc.contributor.authorBligh, Annie Sim Wanen_US
dc.contributor.otherXiong, A.-
dc.contributor.otherYang, L.-
dc.contributor.otherHe, Y.-
dc.contributor.otherZhang, F.-
dc.contributor.otherWang, J.-
dc.contributor.otherHan, H.-
dc.contributor.otherWang, C.-
dc.contributor.otherWang, Z.-
dc.date.accessioned2021-11-15T05:08:46Z-
dc.date.available2021-11-15T05:08:46Z-
dc.date.issued2009-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/1734-
dc.description.abstractHepatotoxic pyrrolizidine alkaloid (HPA)-containing plants have always been a threat to human and livestock health worldwide. Adonifoline, a main HPA in <i>Senecio scandens</i> Buch.-Ham. ex D. Don (Qianli guang), was used officially as an infusion in cases of oral and pharyngeal infections in China. In this study <i>in vivo</i> metabolism of adonifoline was studied for the first time by identifying the metabolites of adonifoline present in bile, urine and feces of rats using liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI-MS<sup>n</sup>) (ion trap) as well as liquid chromatography/electrospray ionization high-resolution mass spectrometry (LC/ESI-HRMS) (quadrupole-time of flight). In total 19 metabolites were identified and, among them, retronecine-<i>N</i>-oxides were confirmed by matching their fragmentation patterns with their fully characterized synthetic compounds. These metabolites are all involved in both phase I and phase II metabolic processes and the principal <i>in vivo</i> metabolism pathways of adonifoline were proposed.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofRapid Communications in Mass Spectrometryen_US
dc.titleIdentification of metabolites of adonifoline, a hepatotoxic pyrrolizidine alkaloid, by liquid chromatography/tandem and high-resolution mass spectrometryen_US
dc.typejournal articleen_US
dc.identifier.doi10.1002/rcm.4329-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn1097-0231en_US
dc.description.volume23en_US
dc.description.issue24en_US
dc.description.startpage3907en_US
dc.description.endpage3916en_US
dc.cihe.affiliatedNo-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.languageiso639-1en-
crisitem.author.deptS.K. Yee School of Health Sciences-
crisitem.author.orcid0000-0002-4757-2159-
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