Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/62148
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dc.contributor.authorSupaporn Kradtap Hartwellen_US
dc.contributor.authorBoonraksa Srisawangen_US
dc.contributor.authorPrachya Kongtawelerten_US
dc.contributor.authorJaroon Jakmuneeen_US
dc.contributor.authorKate Grudpanen_US
dc.date.accessioned2018-09-11T09:22:41Z-
dc.date.available2018-09-11T09:22:41Z-
dc.date.issued2005-04-15en_US
dc.identifier.issn00399140en_US
dc.identifier.other2-s2.0-17744392628en_US
dc.identifier.other10.1016/j.talanta.2004.11.032en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=17744392628&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62148-
dc.description.abstractSequential injection-bead-based immunoassay system has been developed. The main purpose is to make immunoassay process more automated by manipulating the precise delivery of micro-volumes of reagents and the precise timing of incubation and washing steps with a computer program that controls the bi-directional syringe pump. The manifold was designed with the aims of reducing back pressure from beads that act as solid surfaces for immobilization of the target substance, reducing dispersion and dilution of the reagent during incubation, and maximizing signal while minimizing incubation time. This was done by introducing air segment to separate the reagent zone from the carrier stream and by using a suitable sensitive detector which, in this case, was an amperometer. In this study, hyaluronan (HA) was used as a target analyte because of its clinical significance as a potential biomarker for liver, bone and cancer diseases. Amount of hyaluronan was determined using competitive enzyme linked immuno sorbent assay (ELISA) based technique where immobilized HA and HA in solution compete to bind with a fixed amount of biotinylated HA-binding proteins (b-HABPs). Upon separation of the two phases, anti-biotin conjugated with enzyme and a suitable substrate were introduced to follow the binding reaction of the immobilized HA and b-HABPs whose degree of binding is indirectly proportional to the amount of HA in solution. A calibration curve was constructed from a series of concentrations of HA standards. Lowest detectable concentration was found to be 1 ng/mL with the dynamic working range of 1-5000 ng/mL and R.S.D. of intra-assay (n = 7) and inter-assay (n = 3) of various HA concentrations were 4-10% and 9-12%, respectively. Used beads could be reused by washing with 2 M guanidine. Total analysis time for this automatic assay was about 30 min as compared to the 5-8 h used in conventional batch well ELISA. The system could be applied to assay HA in human serum. © 2004 Elsevier B.V. All rights reserved.en_US
dc.subjectChemistryen_US
dc.titleSequential injection-ELISA based system for online determination of hyaluronanen_US
dc.typeJournalen_US
article.title.sourcetitleTalantaen_US
article.volume66en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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