<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yoshikawa H</submitter><funding>Nakatani Foundation for Advancement of Measuring Technologies in Biomedical Engineering</funding><funding>Japan Society for the Promotion of Science</funding><pagination>14510-14514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9082109</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(26)</volume><pubmed_abstract>We evaluated optical pickup ELISA with an original microfluidic disk that contains eight radially arranged channels, which enable semi-automatic sample loading and washing. This disk-shaped chip composed of acrylic plates was fabricated by CO&lt;sub>2&lt;/sub> laser machining and capture antibodies were immobilized in the channels. After the immunoreaction with antigens and enzyme-linked secondary antibodies, an enzyme-catalyzed nanoaggregation of &lt;i>o&lt;/i>-phenylenediamine was detected by measuring the reflectivity change of a laser beam focused in the channel. The assay of C-reactive protein (CRP) was successfully performed in a short amount of time (approximately 20 min from CRP loading). The limit of detection was determined to be 2 ng mL&lt;sup>-1&lt;/sup>, which is more sensitive as compared with</pubmed_abstract><journal>RSC advances</journal><pubmed_title>An optical pickup enzyme-linked immunosorbent assay (ELISA) with a microfluidic disk.</pubmed_title><pmcid>PMC9082109</pmcid><funding_grant_id>15H05769</funding_grant_id><pubmed_authors>Yoshikawa H</pubmed_authors><pubmed_authors>Yoshinaga M</pubmed_authors><pubmed_authors>Tamiya E</pubmed_authors></additional><is_claimable>false</is_claimable><name>An optical pickup enzyme-linked immunosorbent assay (ELISA) with a microfluidic disk.</name><description>We evaluated optical pickup ELISA with an original microfluidic disk that contains eight radially arranged channels, which enable semi-automatic sample loading and washing. This disk-shaped chip composed of acrylic plates was fabricated by CO&lt;sub>2&lt;/sub> laser machining and capture antibodies were immobilized in the channels. After the immunoreaction with antigens and enzyme-linked secondary antibodies, an enzyme-catalyzed nanoaggregation of &lt;i>o&lt;/i>-phenylenediamine was detected by measuring the reflectivity change of a laser beam focused in the channel. The assay of C-reactive protein (CRP) was successfully performed in a short amount of time (approximately 20 min from CRP loading). The limit of detection was determined to be 2 ng mL&lt;sup>-1&lt;/sup>, which is more sensitive as compared with</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2025-04-05T13:24:08.55Z</modification><creation>2025-04-05T13:24:08.55Z</creation></dates><accession>S-EPMC9082109</accession><cross_references><pubmed>35540764</pubmed><doi>10.1039/c8ra01149d</doi></cross_references></HashMap>