Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/61305
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dc.contributor.authorChadarat Duangraten_US
dc.contributor.authorKiattikun Wongsrien_US
dc.contributor.authorYanee Pongpaibulen_US
dc.date.accessioned2018-09-10T04:08:23Z-
dc.date.available2018-09-10T04:08:23Z-
dc.date.issued2007-05-01en_US
dc.identifier.issn15257886en_US
dc.identifier.other2-s2.0-34548285345en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34548285345&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61305-
dc.description.abstractThe aim of this research was to develop and validate a spectrofluorimetric method for determination of tranexamic acid in hydrogel patch formulations. Tranexamic acid (trans-4-aminomethylcyclohexanecarboxylic acid, trans-AMCHA) is an antifibrinolytic drug that recently gained attention as a skin-whitening agent due to its inhibitory effect on ultraviolet (UV)-induced pigmentation in vivo. Derivatization with naphthalene-2,3-dicarboxaldehyde (NDA) in the presence of cyanide ion (CN-) to produce a fluorescent 1-cyanobenz[f] isoindole (CBI) product (λex = 420 nm, λem = 480 nm) is for the first time reported for the determination of tranexamic acid in hydrogel patch formulations. Other separation techniques were not used in the analysis of the CBI-fluorescent product as required in the previous studies. The developed method was proven to be precise and accurate with percent recoveries ranging between 98.0% and 101.8% at the concentration range of 8.4-84,0 μg/ml (R2 > 0.999). The intra- and inter-day precisions as expressed by the relative standard deviations (RSD) were below 1.85%. Derivatization of tranexamic acid with NDA/CN- was completed within five minutes and was stable for at least 30 minutes. The method has been applied to the analysis of drug content and release profiles in tranexamic hydrogel patch formulations.en_US
dc.subjectMedicineen_US
dc.titleSpectrofluorimetric determination of tranexamic acid in hydrogel patch formulations by derivatization with naphthalene-2,3-dicarboxaldehyde/cyanideen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Cosmetic Scienceen_US
article.volume58en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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