{"title":"Development of an Electrochemical Immunosensor for Salivary Oxytocin Determination","authors":"Airi Asano, M. Shiibashi, H. Kudo","doi":"10.1109/BMEICON.2018.8609952","DOIUrl":null,"url":null,"abstract":"A miniaturized electrochemical-oxytocin (OXT) sensor using competitive ELISA was constructed and tested. The OXT sensor measures OXT as reduction of glucose oxidase-labeled oxytocin, which competitively captured by anti-OXT antibodies. We employed a nitrocellulose membrane as a support for antibody because the nitrocellulose membrane improved the output signal by two folds comparing with using a microtiter plate as a support. In the experiment, competitive immunoreaction was first optically measured using conventional biotinylated capture antibody and avidin-GOD. As a result, it was confirmed that oxytocin measurement was possible by the constructed immune system. After that, oxytocin was electrochemically measured on the electrode using a carbon graphite electrode. Redox currents showed a relationship with oxytocin concentration and the calibration range involved 15pg/mL, which has been reported as salivary oxytocin.","PeriodicalId":232271,"journal":{"name":"2018 11th Biomedical Engineering International Conference (BMEiCON)","volume":"35 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2018 11th Biomedical Engineering International Conference (BMEiCON)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BMEICON.2018.8609952","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
A miniaturized electrochemical-oxytocin (OXT) sensor using competitive ELISA was constructed and tested. The OXT sensor measures OXT as reduction of glucose oxidase-labeled oxytocin, which competitively captured by anti-OXT antibodies. We employed a nitrocellulose membrane as a support for antibody because the nitrocellulose membrane improved the output signal by two folds comparing with using a microtiter plate as a support. In the experiment, competitive immunoreaction was first optically measured using conventional biotinylated capture antibody and avidin-GOD. As a result, it was confirmed that oxytocin measurement was possible by the constructed immune system. After that, oxytocin was electrochemically measured on the electrode using a carbon graphite electrode. Redox currents showed a relationship with oxytocin concentration and the calibration range involved 15pg/mL, which has been reported as salivary oxytocin.