In Vitro and In Vivo Electrochemical Measurement of Reactive Oxygen Species After Treatment with Anticancer Drugs

monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and...

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Published inAnalytical chemistry (Washington) Vol. 92; no. 12; pp. 8010 - 8014
Main Authors Vaneev, Alexander N., Gorelkin, Petr V., Garanina, Anastasiia S., Lopatukhina, Helena V., Vodopyanov, Stepan S., Alova, Anna V., Ryabaya, Oxana O., Akasov, Roman A., Zhang, Yanjun, Novak, Pavel, Salikhov, Sergey V., Abakumov, Maxim A., Takahashi, Yasufumi, Edwards, Christopher R. W., Klyachko, Natalia L., Majouga, Alexander G., Korchev, Yuri E., Erofeev, Alexander S.
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 16.06.2020
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Abstract monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and drug-induced ROS production is then recorded. The main advantages of this method are the short incubation time with the drug and its high sensitivity which allows the detection of low intracellular ROS concentrations. We have shown that our new method can measure the ROS response to chemotherapy in tumor-bearing mice in real-time. ROS levels were measured inside the tumor at different depths in response to doxorubicin. This work provides an effective new approach for the measurement of intracellular ROS by platinized nanoelectrodes.
AbstractList In vivo monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and drug-induced ROS production is then recorded. The main advantages of this method are the short incubation time with the drug and its high sensitivity which allows the detection of low intracellular ROS concentrations. We have shown that our new method can measure the ROS response to chemotherapy in tumor-bearing mice in real-time. ROS levels were measured in vivo inside the tumor at different depths in response to doxorubicin. This work provides an effective new approach for the measurement of intracellular ROS by platinized nanoelectrodes.
In vivo monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and drug-induced ROS production is then recorded. The main advantages of this method are the short incubation time with the drug and its high sensitivity which allows the detection of low intracellular ROS concentrations. We have shown that our new method can measure the ROS response to chemotherapy in tumor-bearing mice in real-time. ROS levels were measured in vivo inside the tumor at different depths in response to doxorubicin. This work provides an effective new approach for the measurement of intracellular ROS by platinized nanoelectrodes.In vivo monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and drug-induced ROS production is then recorded. The main advantages of this method are the short incubation time with the drug and its high sensitivity which allows the detection of low intracellular ROS concentrations. We have shown that our new method can measure the ROS response to chemotherapy in tumor-bearing mice in real-time. ROS levels were measured in vivo inside the tumor at different depths in response to doxorubicin. This work provides an effective new approach for the measurement of intracellular ROS by platinized nanoelectrodes.
monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and drug-induced ROS production is then recorded. The main advantages of this method are the short incubation time with the drug and its high sensitivity which allows the detection of low intracellular ROS concentrations. We have shown that our new method can measure the ROS response to chemotherapy in tumor-bearing mice in real-time. ROS levels were measured inside the tumor at different depths in response to doxorubicin. This work provides an effective new approach for the measurement of intracellular ROS by platinized nanoelectrodes.
Author Korchev, Yuri E.
Zhang, Yanjun
Abakumov, Maxim A.
Takahashi, Yasufumi
Edwards, Christopher R. W.
Lopatukhina, Helena V.
Akasov, Roman A.
Ryabaya, Oxana O.
Majouga, Alexander G.
Novak, Pavel
Garanina, Anastasiia S.
Salikhov, Sergey V.
Erofeev, Alexander S.
Gorelkin, Petr V.
Vodopyanov, Stepan S.
Klyachko, Natalia L.
Vaneev, Alexander N.
Alova, Anna V.
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  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia
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  givenname: Anastasiia S.
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  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, Lomonosov Moscow State University, Chemistry Department, Leninskie Gory, 1, 3, Moscow 119991, Russia
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  givenname: Anna V.
  surname: Alova
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  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, Lomonosov Moscow State University, Chemistry Department, Leninskie Gory, 1, 3, Moscow 119991, Russia
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  givenname: Oxana O.
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  organization: N. N. Blokhin National Medical Research Center of Oncology, 24 Kashirskoe shosse, Moscow 115478, Russia
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  surname: Akasov
  fullname: Akasov, Roman A.
  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, I. M. Sechenov First Moscow State Medical University, Trubetskaya Str. 8-2, Moscow 119991, Russia
– sequence: 9
  givenname: Yanjun
  surname: Zhang
  fullname: Zhang, Yanjun
  organization: Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin 300052, China, Imperial College London, Department of Medicine, London W12 0NN, United Kingdom
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  givenname: Pavel
  surname: Novak
  fullname: Novak, Pavel
  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, Imperial College London, Department of Medicine, London W12 0NN, United Kingdom
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  givenname: Sergey V.
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  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia
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  givenname: Maxim A.
  surname: Abakumov
  fullname: Abakumov, Maxim A.
  organization: N. I. Pirogov Russian National Research Medical University, Ostrovityanova Street 1/7, Moscow 117997, Russia
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  givenname: Yasufumi
  orcidid: 0000-0003-2834-8300
  surname: Takahashi
  fullname: Takahashi, Yasufumi
  organization: Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan
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  givenname: Christopher R. W.
  surname: Edwards
  fullname: Edwards, Christopher R. W.
  organization: Imperial College London, Department of Medicine, London W12 0NN, United Kingdom
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  givenname: Natalia L.
  surname: Klyachko
  fullname: Klyachko, Natalia L.
  organization: Lomonosov Moscow State University, Chemistry Department, Leninskie Gory, 1, 3, Moscow 119991, Russia
– sequence: 16
  givenname: Alexander G.
  orcidid: 0000-0002-5184-5551
  surname: Majouga
  fullname: Majouga, Alexander G.
  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, Lomonosov Moscow State University, Chemistry Department, Leninskie Gory, 1, 3, Moscow 119991, Russia, D. Mendeleev University of Chemical Technology of Russia, Miusskaya Square, 9, Moscow 125047, Russia
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  givenname: Yuri E.
  surname: Korchev
  fullname: Korchev, Yuri E.
  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, Imperial College London, Department of Medicine, London W12 0NN, United Kingdom
– sequence: 18
  givenname: Alexander S.
  surname: Erofeev
  fullname: Erofeev, Alexander S.
  organization: National University of Science and Technology “MISiS”, Leninskiy Avenue, 4, Moscow 119049, Russia, Lomonosov Moscow State University, Chemistry Department, Leninskie Gory, 1, 3, Moscow 119991, Russia
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32441506$$D View this record in MEDLINE/PubMed
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Snippet monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in...
In vivo monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action...
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SubjectTerms Analytical chemistry
Animals
Antineoplastic Agents - pharmacology
Antineoplastic drugs
Antitumor agents
Biosensing Techniques
Cancer
cancer therapy
Cell Line, Tumor
Chemistry
Chemotherapy
Doxorubicin
Doxorubicin - pharmacology
Drug development
drug therapy
Drugs
Electrochemical Techniques
Electrochemistry
Humans
Intracellular
mechanism of action
Mice
neoplasms
Neoplasms, Experimental - diagnosis
Neoplasms, Experimental - drug therapy
Neoplasms, Experimental - metabolism
PC-3 Cells
Reactive oxygen species
Reactive Oxygen Species - analysis
Reactive Oxygen Species - antagonists & inhibitors
Reactive Oxygen Species - metabolism
Tumors
Title In Vitro and In Vivo Electrochemical Measurement of Reactive Oxygen Species After Treatment with Anticancer Drugs
URI https://www.ncbi.nlm.nih.gov/pubmed/32441506
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