A nanozyme-linked immunosorbent assay for dual-modal colorimetric and ratiometric fluorescent detection of cardiac troponin I

•A new kind of robust nanozyme-linked immunosorbent assay has been developed.•The proposed nanozyme-linked immunosorbent assay can achieve ratiometric fluorescent and colorimetric dual-modal detection.•This presented method affords robust, reliable and sensitive immunoassay performance. To develop a...

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Vydané v:	Sensors and actuators. B, Chemical Ročník 288; s. 60 - 64
Hlavní autori:	Miao, Luyang, Jiao, Lei, Tang, Qiaorong, Li, He, Zhang, Lianhua, Wei, Qin
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Lausanne Elsevier B.V 01.06.2019 Elsevier Science Ltd
Predmet:	Biomarkers Carbon nitride Colorimetric detecion Colorimetry Dual-modal detection Enzyme-linked immunosorbent assay Fluorescence Hydrogen bonding Hydrogen peroxide Immunoassay Line spectra Peroxidase Phenylenediamine Protein quantification Quantum dots Ratiometric fluorescence Robustness Substrates Ratiometric fluorescence Colorimetric detecion Protein quantification Enzyme-linked immunosorbent assay Dual-modal detection
ISSN:	0925-4005, 1873-3077
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Abstract	•A new kind of robust nanozyme-linked immunosorbent assay has been developed.•The proposed nanozyme-linked immunosorbent assay can achieve ratiometric fluorescent and colorimetric dual-modal detection.•This presented method affords robust, reliable and sensitive immunoassay performance. To develop a robust method for the detection of disease biomarkers is always the pursued goal in the field of biomedical research. Multi-modal immunoassay strategy will bring tremendous potential for the purpose. In this study, a kind of robust nanozyme-linked immunosorbent assay has been presented, which can achieve ratiometric fluorescent and colorimetric dual-modal sensing performance. Here, o-phenylenediamine (OPD) as an organic substrate can be oxidized and converted into 2,3-diaminophenazine (oxOPD) by the robust nanozyme of nanoceria with peroxidase-like properties in the present of H2O2. An exogenous fluorescence signal source of graphitic carbon nitride quantum dots (g-C3N4 QDs) is introduced, and the corresponding fluorescence can be efficiently quenched by oxOPD owing to the hydrogen bonding and π-π stacking interactions, yielding a fluorescence spectral line with dual emission peaks while only irradiated by an excitation wavelength. Meanwhile, a visible color change was derived from the oxOPD formation, which can be recorded by colorimetric method. As a proof-of-study demonstration, the detection of human cardiac troponin I was done. This method affords robust, reliable and sensitive detection performance due to the combination of the merits of ratiometric fluorescent assay and colorimetric assay. It is no doubt that our proposed approach will bring remarkable inspirations for biomedical researchers.
AbstractList	To develop a robust method for the detection of disease biomarkers is always the pursued goal in the field of biomedical research. Multi-modal immunoassay strategy will bring tremendous potential for the purpose. In this study, a kind of robust nanozyme-linked immunosorbent assay has been presented, which can achieve ratiometric fluorescent and colorimetric dual-modal sensing performance. Here, o-phenylenediamine (OPD) as an organic substrate can be oxidized and converted into 2,3-diaminophenazine (oxOPD) by the robust nanozyme of nanoceria with peroxidase-like properties in the present of H2O2. An exogenous fluorescence signal source of graphitic carbon nitride quantum dots (g-C3N4 QDs) is introduced, and the corresponding fluorescence can be efficiently quenched by oxOPD owing to the hydrogen bonding and π-π stacking interactions, yielding a fluorescence spectral line with dual emission peaks while only irradiated by an excitation wavelength. Meanwhile, a visible color change was derived from the oxOPD formation, which can be recorded by colorimetric method. As a proof-of-study demonstration, the detection of human cardiac troponin I was done. This method affords robust, reliable and sensitive detection performance due to the combination of the merits of ratiometric fluorescent assay and colorimetric assay. It is no doubt that our proposed approach will bring remarkable inspirations for biomedical researchers. •A new kind of robust nanozyme-linked immunosorbent assay has been developed.•The proposed nanozyme-linked immunosorbent assay can achieve ratiometric fluorescent and colorimetric dual-modal detection.•This presented method affords robust, reliable and sensitive immunoassay performance. To develop a robust method for the detection of disease biomarkers is always the pursued goal in the field of biomedical research. Multi-modal immunoassay strategy will bring tremendous potential for the purpose. In this study, a kind of robust nanozyme-linked immunosorbent assay has been presented, which can achieve ratiometric fluorescent and colorimetric dual-modal sensing performance. Here, o-phenylenediamine (OPD) as an organic substrate can be oxidized and converted into 2,3-diaminophenazine (oxOPD) by the robust nanozyme of nanoceria with peroxidase-like properties in the present of H2O2. An exogenous fluorescence signal source of graphitic carbon nitride quantum dots (g-C3N4 QDs) is introduced, and the corresponding fluorescence can be efficiently quenched by oxOPD owing to the hydrogen bonding and π-π stacking interactions, yielding a fluorescence spectral line with dual emission peaks while only irradiated by an excitation wavelength. Meanwhile, a visible color change was derived from the oxOPD formation, which can be recorded by colorimetric method. As a proof-of-study demonstration, the detection of human cardiac troponin I was done. This method affords robust, reliable and sensitive detection performance due to the combination of the merits of ratiometric fluorescent assay and colorimetric assay. It is no doubt that our proposed approach will bring remarkable inspirations for biomedical researchers.
Author	Miao, Luyang Tang, Qiaorong Li, He Jiao, Lei Wei, Qin Zhang, Lianhua
Author_xml	– sequence: 1 givenname: Luyang surname: Miao fullname: Miao, Luyang organization: Institute of Surface Analysis and Chemical Biology, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China – sequence: 2 givenname: Lei surname: Jiao fullname: Jiao, Lei organization: College of Optoelectronics Technology, Chengdu University of Information Technology, Chengdu 610225, China – sequence: 3 givenname: Qiaorong surname: Tang fullname: Tang, Qiaorong organization: Institute of Surface Analysis and Chemical Biology, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China – sequence: 4 givenname: He orcidid: 0000-0003-3462-1377 surname: Li fullname: Li, He email: lihecd@gmail.com organization: Institute of Surface Analysis and Chemical Biology, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China – sequence: 5 givenname: Lianhua surname: Zhang fullname: Zhang, Lianhua organization: Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China – sequence: 6 givenname: Qin surname: Wei fullname: Wei, Qin organization: Institute of Surface Analysis and Chemical Biology, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China
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Snippet	•A new kind of robust nanozyme-linked immunosorbent assay has been developed.•The proposed nanozyme-linked immunosorbent assay can achieve ratiometric... To develop a robust method for the detection of disease biomarkers is always the pursued goal in the field of biomedical research. Multi-modal immunoassay...
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SubjectTerms	Biomarkers Carbon nitride Colorimetric detecion Colorimetry Dual-modal detection Enzyme-linked immunosorbent assay Fluorescence Hydrogen bonding Hydrogen peroxide Immunoassay Line spectra Peroxidase Phenylenediamine Protein quantification Quantum dots Ratiometric fluorescence Robustness Substrates
Title	A nanozyme-linked immunosorbent assay for dual-modal colorimetric and ratiometric fluorescent detection of cardiac troponin I
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