Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14932
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dc.contributor.authorSiangproh W.
dc.contributor.authorTeshima N.
dc.contributor.authorSakai T.
dc.contributor.authorKatoh S.
dc.contributor.authorChailapakul O.
dc.date.accessioned2021-04-05T04:32:09Z-
dc.date.available2021-04-05T04:32:09Z-
dc.date.issued2009
dc.identifier.issn399140
dc.identifier.other2-s2.0-67650497907
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14932-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-67650497907&doi=10.1016%2fj.talanta.2008.12.068&partnerID=40&md5=03a6427546a8963fb36b4f0ac9631d9e
dc.description.abstractA simple, automatic and practical system for successive determination of albumin and creatinine has been developed by combining sequential injection analysis (SIA) and highly sensitive dye-binding assays. Albumin detection was based on the increase in the absorbance due to complex formation between albumin and eosin Y in acidic media. The absorbance of the complex was monitored at 547 nm. For the creatinine assay, the concentration of creatinine was measured by reaction with alkaline picrate to form a colored product which absorbs at 500 nm. The influences of experimental variables such as effects of pH, reagent concentration, standard/sample volume and interferences were investigated. Under optimal conditions, the automated method showed linearity up to 20 mg L-1 for albumin and 100 mg L-1 for creatinine. The 3σ detection limits were 0.6 and 3.5 mg L-1 for albumin and creatinine, respectively, and the relative standard deviations (n = 10) were 2.49% for 20 mg L-1 albumin, and 3.14% for 20 mg L-1 creatinine. Application of the proposed method to the direct analysis of urinary samples yielded results which agreed with those obtained from the Bradford protein assay and a creatinine enzymatic assay according to a paired t-test. The results obtained should be a step towards developing a fully automated and reliable analytical system for clinical research, which requires direct determination of albumin and creatinine and/or its ratios. © 2009 Elsevier B.V. All rights reserved.
dc.subjectAlkalinity
dc.subjectClinical research
dc.subjectSpectrophotometry
dc.subjectAlbumin
dc.subjectAlbumin/creatinine ratio (ACR)
dc.subjectCreatinine
dc.subjectSequential injection
dc.subjectUrinary
dc.subjectAssays
dc.titleAlternative method for measurement of albumin/creatinine ratio using spectrophotometric sequential injection analysis
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationTalanta. Vol 79, No.4 (2009), p.1111-1117
dc.identifier.doi10.1016/j.talanta.2008.12.068
Appears in Collections:Scopus 1983-2021

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