A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection
Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for e...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Yang, Huaixia [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023transfer abstract |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications - Mohamed, S.H. ELSEVIER, 2019, the international journal of pure and applied analytical chemistry, Amsterdam [u.a.] |
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| Übergeordnetes Werk: |
volume:253 ; year:2023 ; day:1 ; month:02 ; pages:0 |
| Links: |
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| DOI / URN: |
10.1016/j.talanta.2022.124059 |
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| 520 | |a Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. | ||
| 520 | |a Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. | ||
| 650 | 7 | |a Exosome |2 Elsevier | |
| 650 | 7 | |a ARGET ATRP |2 Elsevier | |
| 650 | 7 | |a Fluorescence |2 Elsevier | |
| 650 | 7 | |a Sensor |2 Elsevier | |
| 700 | 1 | |a Jin, Zhenyu |4 oth | |
| 700 | 1 | |a Cui, Zhenzhen |4 oth | |
| 700 | 1 | |a Guo, Liang |4 oth | |
| 700 | 1 | |a Kong, Jinming |4 oth | |
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10.1016/j.talanta.2022.124059 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001983.pica (DE-627)ELV059757620 (ELSEVIER)S0039-9140(22)00855-4 DE-627 ger DE-627 rakwb eng 530 620 VZ 53.56 bkl Yang, Huaixia verfasserin aut A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection 2023transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosome Elsevier ARGET ATRP Elsevier Fluorescence Elsevier Sensor Elsevier Jin, Zhenyu oth Cui, Zhenzhen oth Guo, Liang oth Kong, Jinming oth Enthalten in Elsevier Science Mohamed, S.H. ELSEVIER Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications 2019 the international journal of pure and applied analytical chemistry Amsterdam [u.a.] (DE-627)ELV003060667 volume:253 year:2023 day:1 month:02 pages:0 https://doi.org/10.1016/j.talanta.2022.124059 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.56 Halbleitertechnologie VZ AR 253 2023 1 0201 0 |
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10.1016/j.talanta.2022.124059 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001983.pica (DE-627)ELV059757620 (ELSEVIER)S0039-9140(22)00855-4 DE-627 ger DE-627 rakwb eng 530 620 VZ 53.56 bkl Yang, Huaixia verfasserin aut A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection 2023transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosome Elsevier ARGET ATRP Elsevier Fluorescence Elsevier Sensor Elsevier Jin, Zhenyu oth Cui, Zhenzhen oth Guo, Liang oth Kong, Jinming oth Enthalten in Elsevier Science Mohamed, S.H. ELSEVIER Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications 2019 the international journal of pure and applied analytical chemistry Amsterdam [u.a.] (DE-627)ELV003060667 volume:253 year:2023 day:1 month:02 pages:0 https://doi.org/10.1016/j.talanta.2022.124059 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.56 Halbleitertechnologie VZ AR 253 2023 1 0201 0 |
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10.1016/j.talanta.2022.124059 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001983.pica (DE-627)ELV059757620 (ELSEVIER)S0039-9140(22)00855-4 DE-627 ger DE-627 rakwb eng 530 620 VZ 53.56 bkl Yang, Huaixia verfasserin aut A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection 2023transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosome Elsevier ARGET ATRP Elsevier Fluorescence Elsevier Sensor Elsevier Jin, Zhenyu oth Cui, Zhenzhen oth Guo, Liang oth Kong, Jinming oth Enthalten in Elsevier Science Mohamed, S.H. ELSEVIER Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications 2019 the international journal of pure and applied analytical chemistry Amsterdam [u.a.] (DE-627)ELV003060667 volume:253 year:2023 day:1 month:02 pages:0 https://doi.org/10.1016/j.talanta.2022.124059 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.56 Halbleitertechnologie VZ AR 253 2023 1 0201 0 |
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10.1016/j.talanta.2022.124059 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001983.pica (DE-627)ELV059757620 (ELSEVIER)S0039-9140(22)00855-4 DE-627 ger DE-627 rakwb eng 530 620 VZ 53.56 bkl Yang, Huaixia verfasserin aut A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection 2023transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosome Elsevier ARGET ATRP Elsevier Fluorescence Elsevier Sensor Elsevier Jin, Zhenyu oth Cui, Zhenzhen oth Guo, Liang oth Kong, Jinming oth Enthalten in Elsevier Science Mohamed, S.H. ELSEVIER Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications 2019 the international journal of pure and applied analytical chemistry Amsterdam [u.a.] (DE-627)ELV003060667 volume:253 year:2023 day:1 month:02 pages:0 https://doi.org/10.1016/j.talanta.2022.124059 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.56 Halbleitertechnologie VZ AR 253 2023 1 0201 0 |
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10.1016/j.talanta.2022.124059 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001983.pica (DE-627)ELV059757620 (ELSEVIER)S0039-9140(22)00855-4 DE-627 ger DE-627 rakwb eng 530 620 VZ 53.56 bkl Yang, Huaixia verfasserin aut A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection 2023transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. Exosome Elsevier ARGET ATRP Elsevier Fluorescence Elsevier Sensor Elsevier Jin, Zhenyu oth Cui, Zhenzhen oth Guo, Liang oth Kong, Jinming oth Enthalten in Elsevier Science Mohamed, S.H. ELSEVIER Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications 2019 the international journal of pure and applied analytical chemistry Amsterdam [u.a.] (DE-627)ELV003060667 volume:253 year:2023 day:1 month:02 pages:0 https://doi.org/10.1016/j.talanta.2022.124059 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.56 Halbleitertechnologie VZ AR 253 2023 1 0201 0 |
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Enthalten in Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications Amsterdam [u.a.] volume:253 year:2023 day:1 month:02 pages:0 |
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Enthalten in Optical, water splitting and wettability of titanium nitride/titanium oxynitride bilayer films for hydrogen generation and solar cells applications Amsterdam [u.a.] volume:253 year:2023 day:1 month:02 pages:0 |
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a specific sensor system based on in-situ synthesis fluorescent polymers by arget atrp achieving sensitive exosome detection |
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A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection |
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Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. |
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Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. |
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Exosomes, as a kind of tumor biomarker, are often found at elevated levels above normal in the blood of cancer patients, making highly sensitive exosome testing important for monitoring the development and progression of cancer. In this work, an ultra-sensitive and specific fluorescence method for exosome assays was constructed on the basis of atom transfer radical polymerization (ATRP) technique. Firstly, two recognition units, the CD63 aptamer and the EGFR antibody, can specifically bind to exosomes to form a sandwich structure, which endows the proposed sensor with excellent selectivity through two specific recognitions. Secondly, activator regenerated by electron transfer ATRP (ARGET ATRP) polymerization amplification method can introduce a huge amount of the fluorescent monomers into the sensing system, leading to a marked rise in sensitivity. Under optimal experimental conditions, a clear linear relationship between the logarithm of the fluorescence intensity and the concentration of exosomes in the range of 5 × 104 exosomes/mL to 5 × 109 exosomes/mL was obtained. The limit of detection (LOD) was as low as 11,610 exosomes/mL. Furthermore, this sensor exhibited good selectivity and stability, and excellent immunity to interference, providing a new method for the detection of exosomes. The exosome detection strategy used in this system provides a new idea for effective detection of lung cancer at an early stage. |
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A specific sensor system based on in-situ synthesis fluorescent polymers by ARGET ATRP achieving sensitive exosome detection |
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