<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gutierrez-Galvez L</submitter><funding>EU</funding><funding>MINECO</funding><funding>Spanish Ministry of Universities</funding><funding>MINECO,SEVERO OCHOA</funding><funding>CM</funding><funding>Community of Madrid</funding><funding>Spanish Ministry of Economy and Competitiveness</funding><pagination>348</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10046281</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(3)</volume><pubmed_abstract>In this work, we present the combination of two different types of nanomaterials, 2D molybdenum disulfide nanosheets (MoS&lt;sub>2&lt;/sub>-NS) and zero-dimensional carbon nanodots (CDs), for the development of a new electrochemiluminescence (ECL) platform for the early detection and quantification of the biomarker human epidermal growth factor receptor 2 (HER2), whose overexpression is associated with breast cancer. MoS&lt;sub>2&lt;/sub>-NS are used as an immobilization platform for the thiolated aptamer, which can recognize the HER2 epitope peptide with high affinity, and CDs act as coreactants of the anodic oxidation of the luminophore [Ru(bpy)&lt;sub>3&lt;/sub>]&lt;sup>2+&lt;/sup>. The HER2 biomarker is detected by changes in the ECL signal of the [Ru(bpy)&lt;sub>3&lt;/sub>]&lt;sup>2+&lt;/sup>/CD system, with a low detection limit of 1.84 fg/mL and a wide linear range. The proposed method has been successfully applied to detect the HER2 biomarker in human serum samples.</pubmed_abstract><journal>Biosensors</journal><pubmed_title>MoS&lt;sub>2&lt;/sub>-Carbon Nanodots as a New Electrochemiluminescence Platform for Breast Cancer Biomarker Detection.</pubmed_title><pmcid>PMC10046281</pmcid><funding_grant_id>PID2020-116728RB-I00, PID2020-116661RB-I00, CTQ2015-71955-REDT (ELECTROBIONET)</funding_grant_id><funding_grant_id>Grant CEX2020-001039-S</funding_grant_id><funding_grant_id>TRANSNANOAVANSENS, S2018/NMT-4349, and FotoArt (P2018/NMT-4367</funding_grant_id><funding_grant_id>project S2018/NMT-4291 TEC2SPACE</funding_grant_id><funding_grant_id>FPU19/06309</funding_grant_id><funding_grant_id>project CSIC13-4E-1794</funding_grant_id><funding_grant_id>FEDER, FSE</funding_grant_id><pubmed_authors>Perez EM</pubmed_authors><pubmed_authors>Sulleiro MV</pubmed_authors><pubmed_authors>Garcia-Mendiola T</pubmed_authors><pubmed_authors>Lorenzo E</pubmed_authors><pubmed_authors>Gutierrez-Galvez L</pubmed_authors><pubmed_authors>Gutierrez-Sanchez C</pubmed_authors><pubmed_authors>Luna M</pubmed_authors><pubmed_authors>Garcia-Nieto D</pubmed_authors></additional><is_claimable>false</is_claimable><name>MoS&lt;sub>2&lt;/sub>-Carbon Nanodots as a New Electrochemiluminescence Platform for Breast Cancer Biomarker Detection.</name><description>In this work, we present the combination of two different types of nanomaterials, 2D molybdenum disulfide nanosheets (MoS&lt;sub>2&lt;/sub>-NS) and zero-dimensional carbon nanodots (CDs), for the development of a new electrochemiluminescence (ECL) platform for the early detection and quantification of the biomarker human epidermal growth factor receptor 2 (HER2), whose overexpression is associated with breast cancer. MoS&lt;sub>2&lt;/sub>-NS are used as an immobilization platform for the thiolated aptamer, which can recognize the HER2 epitope peptide with high affinity, and CDs act as coreactants of the anodic oxidation of the luminophore [Ru(bpy)&lt;sub>3&lt;/sub>]&lt;sup>2+&lt;/sup>. The HER2 biomarker is detected by changes in the ECL signal of the [Ru(bpy)&lt;sub>3&lt;/sub>]&lt;sup>2+&lt;/sup>/CD system, with a low detection limit of 1.84 fg/mL and a wide linear range. The proposed method has been successfully applied to detect the HER2 biomarker in human serum samples.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2024-10-17T22:13:12.972Z</modification><creation>2024-10-17T22:13:12.972Z</creation></dates><accession>S-EPMC10046281</accession><cross_references><pubmed>36979560</pubmed><doi>10.3390/bios13030348</doi></cross_references></HashMap>