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      Amphiphilic Fluorine-Containing Block Copolymers as Carriers for Hydrophobic PtTFPP for Dissolved Oxygen Sensing, Cell Respiration Monitoring and In Vivo Hypoxia Imaging with High Quantum Efficiency and Long Lifetime

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          Abstract

          New amphiphilic star or multi-arm block copolymers with different structures were synthesized for enabling the use of hydrophobic oxygen probe of platinum (II)-tetrakis (pentafluorophenyl) porphyrin (PtTFPP) for bioanalysis. The amphiphilic star polymers were prepared through the Atom Transfer Radical Polymerization (ATRP) method by using hydrophilic 4-arm polyethylene glycol (4-arm-PEG) as an initiator. Among the five block copolymers, P1 series ( P1a, P1b, and P1c) and P3 possess fluorine-containing moieties to improve the oxygen sensitivity with its excellent capacity to dissolve and carry oxygen. A polymer P2 without fluorine units was also synthesized for comparison. The structure-property relationship was investigated. Under nitrogen atmosphere, high quantum efficiency of PtTFPP in fluorine-containing micelles could reach to 22% and long lifetime could reach to 76 μs. One kind of representative PtTFPP-containing micelles was used to detect the respiration of Escherichia coli ( E. coli) JM109 and macrophage cell J774A.1 by a high throughput plate reader. In vivo hypoxic imaging of tumor-bearing mice was also achieved successfully. This study demonstrated that using well-designed fluoropolymers to load PtTFPP could achieve high oxygen sensing properties, and long lifetime, showing the great capability for further in vivo sensing and imaging.

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          Most cited references45

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          Atom Transfer Radical Polymerization (ATRP): Current Status and Future Perspectives

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            Tumor hypoxia causes DNA hypermethylation by reducing TET activity

            Summary Hypermethylation of tumor suppressor gene (TSG) promoters confers growth advantages to cancer cells, but how these changes arise is poorly understood. Here, we report that tumor hypoxia reduces the activity of oxygen-dependent TET enzymes, which catalyze DNA de-methylation through 5-methylcytosine oxidation. This occurs independently of hypoxia-associated alterations in TET expression, proliferation, metabolism, HIF activity or reactive oxygen, but directly depends on oxygen shortage. Hypoxia-induced loss of TET activity increases hypermethylation at gene promoters in vitro. Also in patients, TSG promoters are markedly more methylated in hypoxic tumors, independently of proliferation, stromal cell infiltration and tumor characteristics. Our data suggest cellular selection of hypermethylation events, with almost half of them being ascribable to hypoxia across tumor types. Accordingly, increased hypoxia after vessel pruning in murine breast tumors increases hypermethylation, while restored tumor oxygenation by vessel normalization abrogates this effect. Tumor hypoxia thus acts as a novel regulator underlying DNA methylation.
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              Detection and characterization of tumor hypoxia using pO2 histography.

              Data from 125 studies describing the pretreatment oxygenation status as measured in the clinical setting using the computerized Eppendorf pO2 histography system have been compiled in this article. Tumor oxygenation is heterogeneous and severely compromised as compared to normal tissue. Hypoxia results from inadequate perfusion and diffusion within tumors and from a reduced O2 transport capacity in anemic patients. The development of tumor hypoxia is independent of a series of relevant tumor characteristics (e.g., clinical size, stage, histology, and grade) and various patient demographics. Overall median pO2 in cancers of the uterine cervix, head and neck, and breast is 10 mm Hg with the overall hypoxic fraction (pO2
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                Author and article information

                Journal
                Sensors (Basel)
                Sensors (Basel)
                sensors
                Sensors (Basel, Switzerland)
                MDPI
                1424-8220
                02 November 2018
                November 2018
                : 18
                : 11
                : 3752
                Affiliations
                [1 ]School of Materials Science and Engineering, Harbin Institute of Technology, Nangang District, Harbin 150001, China; 11749240@ 123456mail.sustc.edu.cn
                [2 ]Department of Materials Science and Engineering, Southern University of Science and Technology, Xili, Nanshan District, Shenzhen 518055, China; qiaoy@ 123456mail.sustc.edu.cn (Y.Q.); 11553010@ 123456mail.sustc.edu.cn (T.P.); 11612419@ 123456mail.sustc.edu.cn (K.Z.); 11510869@ 123456mail.sustc.edu.cn (J.W.); 2018090123@ 123456gdip.edu.cn (S.W.)
                [3 ]Light Chemical Technology College, Guangdong Industry Polytechnic, Haizhu District, Guangzhou 510300, China
                [4 ]SUSTech Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Xili, Nanshan District, Shenzhen 518055, China
                Author notes
                [* ]Correspondence: fysu@ 123456sustc.edu.cn (F.S.); tianyq@ 123456sustc.edu.cn (Y.T.); Tel.: +86-755-8801-8997
                Author information
                https://orcid.org/0000-0002-1441-2431
                Article
                sensors-18-03752
                10.3390/s18113752
                6263385
                30400255
                6e01fdf0-3184-496c-950f-6abbeeaba79f
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 03 October 2018
                : 29 October 2018
                Categories
                Article

                Biomedical engineering
                dissolved oxygen sensors,fluoropolymers,micelles,cell respiration monitoring,tumor imaging

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