<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang G</submitter><funding>Basic Research Fund for Nonprofit Research Institutes in Fujian (Mindong Fisheries Research Institute of Fujian Province, China, 2021R1036-3)</funding><funding>the Special Research Fund for the National Non-profit Institutes (East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, China)</funding><funding>Central Public-interest Scientific Institution Basal Research Fund, CAFS</funding><funding>National Natural Science Foundation of China</funding><pagination>38</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9855656</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Malachite green (MG) is a synthetic poisonous organic compound that has been banned in many countries as a veterinary drug for aquaculture. An efficient, fast and sensitive method is urgently needed for monitoring the illegal use of malachite green (MG) in aquaculture. In this study, a novel ratiometric fluorescence immunoassay was established. Nitrogen-doped carbon quantum dots were used as ratiometric fluorescent probes with a fluorescence peak at 450 nm. Horseradish peroxidase was employed to convert o-phenylenediamine to 2,3-diaminophenazine, with a new fluorescence peak at 580 nm and a strong absorption at 420 nm. The inner filter effect between N-CQD fluorescence and DAP absorption was identified. It allows for the ratiometric detection of MG using a fluorescent immunoassay. The results demonstrated a linear ratiometric fluorescence response for MG between 0.1 and 12.8 ng·mL&lt;sup>-1&lt;/sup>. The limit of detection of this method was verified to be 0.097 μg·kg&lt;sup>-1&lt;/sup> with recoveries ranging from 81.88 to 108%, and the relative standard deviations were below 3%. Furthermore, this method exhibited acceptable consistency with the LC-MS/MS results when applied for MG screening in real samples. These results demonstrated a promising application of this novel ratiometric fluorescence immunoassay for MG screening with the merits of rapid detection, simple sample preparation, and stable signal readout. It can be an alternative to other traditional methods if there are difficulties in the availability of expensive instruments, and achieve comparable results or even more sensitivity than other reported methods.</pubmed_abstract><journal>Biosensors</journal><pubmed_title>Ratiometric Fluorescence Immunoassay Based on Carbon Quantum Dots for Sensitive Detection of Malachite Green in Fish.</pubmed_title><pmcid>PMC9855656</pmcid><funding_grant_id>2020TD72</funding_grant_id><funding_grant_id>2016T09</funding_grant_id><funding_grant_id>31701698</funding_grant_id><funding_grant_id>2021R1036-3</funding_grant_id><pubmed_authors>Yang G</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Fodjo EK</pubmed_authors><pubmed_authors>Zhai W</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Gu L</pubmed_authors><pubmed_authors>Kong C</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ratiometric Fluorescence Immunoassay Based on Carbon Quantum Dots for Sensitive Detection of Malachite Green in Fish.</name><description>Malachite green (MG) is a synthetic poisonous organic compound that has been banned in many countries as a veterinary drug for aquaculture. An efficient, fast and sensitive method is urgently needed for monitoring the illegal use of malachite green (MG) in aquaculture. In this study, a novel ratiometric fluorescence immunoassay was established. Nitrogen-doped carbon quantum dots were used as ratiometric fluorescent probes with a fluorescence peak at 450 nm. Horseradish peroxidase was employed to convert o-phenylenediamine to 2,3-diaminophenazine, with a new fluorescence peak at 580 nm and a strong absorption at 420 nm. The inner filter effect between N-CQD fluorescence and DAP absorption was identified. It allows for the ratiometric detection of MG using a fluorescent immunoassay. The results demonstrated a linear ratiometric fluorescence response for MG between 0.1 and 12.8 ng·mL&lt;sup>-1&lt;/sup>. The limit of detection of this method was verified to be 0.097 μg·kg&lt;sup>-1&lt;/sup> with recoveries ranging from 81.88 to 108%, and the relative standard deviations were below 3%. Furthermore, this method exhibited acceptable consistency with the LC-MS/MS results when applied for MG screening in real samples. These results demonstrated a promising application of this novel ratiometric fluorescence immunoassay for MG screening with the merits of rapid detection, simple sample preparation, and stable signal readout. It can be an alternative to other traditional methods if there are difficulties in the availability of expensive instruments, and achieve comparable results or even more sensitivity than other reported methods.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-26T00:38:50.594Z</modification><creation>2025-04-06T09:47:35.058Z</creation></dates><accession>S-EPMC9855656</accession><cross_references><pubmed>36671873</pubmed><doi>10.3390/bios13010038</doi></cross_references></HashMap>