Diketopyrrolopyrrole-based sensor for over-expressed peroxynitrite in drug-induced hepatotoxicity via ratiometric fluorescence imaging

Early diagnosis and detection of drug-induced liver injury (DILI) is great significance for the effective prevention and treatment of patients with liver injury. Studies indicate that the up-regulation of peroxynitrite (ONOO−) levels in liver is profoundly involved in acetaminophen (APAP)-induced li...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2022-02, Vol.352, p.130992, Article 130992
Hauptverfasser: Wang, Nannan, Wang, Han, Zhang, Jian, Ji, Xin, Su, Huihui, Liu, Jinying, Wang, Jiamin, Zhao, Weili
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container_start_page 130992
container_title Sensors and actuators. B, Chemical
container_volume 352
creator Wang, Nannan
Wang, Han
Zhang, Jian
Ji, Xin
Su, Huihui
Liu, Jinying
Wang, Jiamin
Zhao, Weili
description Early diagnosis and detection of drug-induced liver injury (DILI) is great significance for the effective prevention and treatment of patients with liver injury. Studies indicate that the up-regulation of peroxynitrite (ONOO−) levels in liver is profoundly involved in acetaminophen (APAP)-induced liver injury. Herein, we constructed diketopyrrolopyrrole (DPP)-based ratiometric fluorescent probes (DPP-DH-P and DPP-DEG-P) for detecting and imaging ONOO−. Comparing two probes, DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold) and lower detection limit (3.5 nM) for tracking ONOO− in solution. DPP-DH-P possessing better biocompatibility had been successfully applied to monitor the fluctuation of ONOO− in LPS/IFN-γ or APAP-treated hepatocytes with a high signal-to-noise ratio (20-fold) by ratiometric imaging. Moreover, the probe was used to evaluate the repair effect of glutathione on DILI. We unexpectedly discovered that DPP-DH-P and DPP-DH targeted lysosomes and mitochondria, respectively. Based on the change of ONOO− induced by APAP, we observed that DPP-DH-P and the generated DPP-DH diffused from lysosome into cytoplasm, and DPP-DH did not target mitochondria due to the effect of endogenous ONOO−, these indirectly reflected the dysfunction of organelles. Observably, this work will accelerate a deeper comprehending for the pathogenesis of DILI, and furnish an effective tool for the diagnosis and treatment of DILI. [Display omitted] •Two ratiometric fluorescent probes DPP-DH-P and DPP-DEG-P with ICT characteristic for imaging ONOO− were reported.•DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold vs 353-fold) and lower detection limit (3.5 nM vs 8.4 nM).•DPP-DH-P could be used to visualize ONOO− by ratiometric fluorescence imaging in living cells and in vivo.•DPP-DH-P realized the diagnosis and detection of APAP-induced hepatotoxicity, and also evaluated the repair effect of GSH.•The changes in the targeting ability of DPP-DH-P and generated DPP-DH indirectly reflected the dysfunction of organelles.
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Studies indicate that the up-regulation of peroxynitrite (ONOO−) levels in liver is profoundly involved in acetaminophen (APAP)-induced liver injury. Herein, we constructed diketopyrrolopyrrole (DPP)-based ratiometric fluorescent probes (DPP-DH-P and DPP-DEG-P) for detecting and imaging ONOO−. Comparing two probes, DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold) and lower detection limit (3.5 nM) for tracking ONOO− in solution. DPP-DH-P possessing better biocompatibility had been successfully applied to monitor the fluctuation of ONOO− in LPS/IFN-γ or APAP-treated hepatocytes with a high signal-to-noise ratio (20-fold) by ratiometric imaging. Moreover, the probe was used to evaluate the repair effect of glutathione on DILI. We unexpectedly discovered that DPP-DH-P and DPP-DH targeted lysosomes and mitochondria, respectively. Based on the change of ONOO− induced by APAP, we observed that DPP-DH-P and the generated DPP-DH diffused from lysosome into cytoplasm, and DPP-DH did not target mitochondria due to the effect of endogenous ONOO−, these indirectly reflected the dysfunction of organelles. Observably, this work will accelerate a deeper comprehending for the pathogenesis of DILI, and furnish an effective tool for the diagnosis and treatment of DILI. [Display omitted] •Two ratiometric fluorescent probes DPP-DH-P and DPP-DEG-P with ICT characteristic for imaging ONOO− were reported.•DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold vs 353-fold) and lower detection limit (3.5 nM vs 8.4 nM).•DPP-DH-P could be used to visualize ONOO− by ratiometric fluorescence imaging in living cells and in vivo.•DPP-DH-P realized the diagnosis and detection of APAP-induced hepatotoxicity, and also evaluated the repair effect of GSH.•The changes in the targeting ability of DPP-DH-P and generated DPP-DH indirectly reflected the dysfunction of organelles.</description><identifier>ISSN: 0925-4005</identifier><identifier>EISSN: 1873-3077</identifier><identifier>DOI: 10.1016/j.snb.2021.130992</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Biocompatibility ; Bioimaging ; Cytoplasm ; Diagnosis ; Drug-induced liver injury ; Fluorescent indicators ; Fluorescent probe ; Glutathione ; Injury prevention ; Liver ; Lysosomes ; Medical imaging ; Mitochondria ; Organelles ; Pathogenesis ; Peroxynitrite ; Signal to noise ratio ; Subcellular localization</subject><ispartof>Sensors and actuators. 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B, Chemical</title><description>Early diagnosis and detection of drug-induced liver injury (DILI) is great significance for the effective prevention and treatment of patients with liver injury. Studies indicate that the up-regulation of peroxynitrite (ONOO−) levels in liver is profoundly involved in acetaminophen (APAP)-induced liver injury. Herein, we constructed diketopyrrolopyrrole (DPP)-based ratiometric fluorescent probes (DPP-DH-P and DPP-DEG-P) for detecting and imaging ONOO−. Comparing two probes, DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold) and lower detection limit (3.5 nM) for tracking ONOO− in solution. DPP-DH-P possessing better biocompatibility had been successfully applied to monitor the fluctuation of ONOO− in LPS/IFN-γ or APAP-treated hepatocytes with a high signal-to-noise ratio (20-fold) by ratiometric imaging. Moreover, the probe was used to evaluate the repair effect of glutathione on DILI. We unexpectedly discovered that DPP-DH-P and DPP-DH targeted lysosomes and mitochondria, respectively. Based on the change of ONOO− induced by APAP, we observed that DPP-DH-P and the generated DPP-DH diffused from lysosome into cytoplasm, and DPP-DH did not target mitochondria due to the effect of endogenous ONOO−, these indirectly reflected the dysfunction of organelles. Observably, this work will accelerate a deeper comprehending for the pathogenesis of DILI, and furnish an effective tool for the diagnosis and treatment of DILI. [Display omitted] •Two ratiometric fluorescent probes DPP-DH-P and DPP-DEG-P with ICT characteristic for imaging ONOO− were reported.•DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold vs 353-fold) and lower detection limit (3.5 nM vs 8.4 nM).•DPP-DH-P could be used to visualize ONOO− by ratiometric fluorescence imaging in living cells and in vivo.•DPP-DH-P realized the diagnosis and detection of APAP-induced hepatotoxicity, and also evaluated the repair effect of GSH.•The changes in the targeting ability of DPP-DH-P and generated DPP-DH indirectly reflected the dysfunction of organelles.</description><subject>Biocompatibility</subject><subject>Bioimaging</subject><subject>Cytoplasm</subject><subject>Diagnosis</subject><subject>Drug-induced liver injury</subject><subject>Fluorescent indicators</subject><subject>Fluorescent probe</subject><subject>Glutathione</subject><subject>Injury prevention</subject><subject>Liver</subject><subject>Lysosomes</subject><subject>Medical imaging</subject><subject>Mitochondria</subject><subject>Organelles</subject><subject>Pathogenesis</subject><subject>Peroxynitrite</subject><subject>Signal to noise ratio</subject><subject>Subcellular localization</subject><issn>0925-4005</issn><issn>1873-3077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE1PwzAMhiMEEmPwA7hV4tySpN_ihManNIkLnKM0cUfK1hQnndY_wO8m1ThzsOzI72s7DyHXjCaMsuK2S1zfJJxylrCU1jU_IQtWlWmc0rI8JQta8zzOKM3PyYVzHaU0Swu6ID8P5gu8HSZEu_1LEDfSgY4c9M5i1Iawe8AYDgOCmzsDoD1MvfFoPESmjzSOm9j0elSh-wmD9Nbbg1HGT9HeyAilN3YHQa-idjvaMEdBr4J3Jzem31ySs1ZuHVz95SX5eHp8X73E67fn19X9OlY8z31cVxnntWwlk0zXoWRctYxC2WRc80KVTZWrTDHFm7pSmkvJM6lYmrImPFqaLsnNce6A9nsE50VnR-zDSsELXgZuBZ9V7KhSaJ1DaMWA4VCcBKNixi06EXCLGbc44g6eu6MHwvl7AyicMvMXtUFQXmhr_nH_AiAdjLQ</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Wang, Nannan</creator><creator>Wang, Han</creator><creator>Zhang, Jian</creator><creator>Ji, Xin</creator><creator>Su, Huihui</creator><creator>Liu, Jinying</creator><creator>Wang, Jiamin</creator><creator>Zhao, Weili</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20220201</creationdate><title>Diketopyrrolopyrrole-based sensor for over-expressed peroxynitrite in drug-induced hepatotoxicity via ratiometric fluorescence imaging</title><author>Wang, Nannan ; Wang, Han ; Zhang, Jian ; Ji, Xin ; Su, Huihui ; Liu, Jinying ; Wang, Jiamin ; Zhao, Weili</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c255t-984229afa1a1d922912cf10e7b42d26c7b85c4c1c2b98cd2aa24ac1331bd2af03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biocompatibility</topic><topic>Bioimaging</topic><topic>Cytoplasm</topic><topic>Diagnosis</topic><topic>Drug-induced liver injury</topic><topic>Fluorescent indicators</topic><topic>Fluorescent probe</topic><topic>Glutathione</topic><topic>Injury prevention</topic><topic>Liver</topic><topic>Lysosomes</topic><topic>Medical imaging</topic><topic>Mitochondria</topic><topic>Organelles</topic><topic>Pathogenesis</topic><topic>Peroxynitrite</topic><topic>Signal to noise ratio</topic><topic>Subcellular localization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Nannan</creatorcontrib><creatorcontrib>Wang, Han</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>Ji, Xin</creatorcontrib><creatorcontrib>Su, Huihui</creatorcontrib><creatorcontrib>Liu, Jinying</creatorcontrib><creatorcontrib>Wang, Jiamin</creatorcontrib><creatorcontrib>Zhao, Weili</creatorcontrib><collection>CrossRef</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Sensors and actuators. 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Studies indicate that the up-regulation of peroxynitrite (ONOO−) levels in liver is profoundly involved in acetaminophen (APAP)-induced liver injury. Herein, we constructed diketopyrrolopyrrole (DPP)-based ratiometric fluorescent probes (DPP-DH-P and DPP-DEG-P) for detecting and imaging ONOO−. Comparing two probes, DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold) and lower detection limit (3.5 nM) for tracking ONOO− in solution. DPP-DH-P possessing better biocompatibility had been successfully applied to monitor the fluctuation of ONOO− in LPS/IFN-γ or APAP-treated hepatocytes with a high signal-to-noise ratio (20-fold) by ratiometric imaging. Moreover, the probe was used to evaluate the repair effect of glutathione on DILI. We unexpectedly discovered that DPP-DH-P and DPP-DH targeted lysosomes and mitochondria, respectively. Based on the change of ONOO− induced by APAP, we observed that DPP-DH-P and the generated DPP-DH diffused from lysosome into cytoplasm, and DPP-DH did not target mitochondria due to the effect of endogenous ONOO−, these indirectly reflected the dysfunction of organelles. Observably, this work will accelerate a deeper comprehending for the pathogenesis of DILI, and furnish an effective tool for the diagnosis and treatment of DILI. [Display omitted] •Two ratiometric fluorescent probes DPP-DH-P and DPP-DEG-P with ICT characteristic for imaging ONOO− were reported.•DPP-DEG-P exhibited higher signal-to-noise ratio (2750-fold vs 353-fold) and lower detection limit (3.5 nM vs 8.4 nM).•DPP-DH-P could be used to visualize ONOO− by ratiometric fluorescence imaging in living cells and in vivo.•DPP-DH-P realized the diagnosis and detection of APAP-induced hepatotoxicity, and also evaluated the repair effect of GSH.•The changes in the targeting ability of DPP-DH-P and generated DPP-DH indirectly reflected the dysfunction of organelles.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.snb.2021.130992</doi></addata></record>
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subjects Biocompatibility
Bioimaging
Cytoplasm
Diagnosis
Drug-induced liver injury
Fluorescent indicators
Fluorescent probe
Glutathione
Injury prevention
Liver
Lysosomes
Medical imaging
Mitochondria
Organelles
Pathogenesis
Peroxynitrite
Signal to noise ratio
Subcellular localization
title Diketopyrrolopyrrole-based sensor for over-expressed peroxynitrite in drug-induced hepatotoxicity via ratiometric fluorescence imaging
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