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A Glutathione Activatable Photosensitizer for Combined Photodynamic and Gas Therapy under Red Light Irradiation
Although photodynamic therapy (PDT) is a promising approach for cancer therapy, most existing photosensitizers lack selectivity for tumor cells and the overexpressed glutathione (GSH) in tumor cells reduces the PDT efficiency. Therefore, designing photosensitizers that can be selectively activated w...
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Published in: | Advanced healthcare materials 2022-02, Vol.11 (4), p.e2102017-n/a |
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description | Although photodynamic therapy (PDT) is a promising approach for cancer therapy, most existing photosensitizers lack selectivity for tumor cells and the overexpressed glutathione (GSH) in tumor cells reduces the PDT efficiency. Therefore, designing photosensitizers that can be selectively activated within tumor cells and combine PDT with other therapeutic modalities represents a route for precise and efficient anticancer treatment. Herein, an organic activatable photosensitizer, CyI‐DNBS, bearing 2,4‐dinitrobenzenesulfonate (DNBS) as the cage group is reported. CyI‐DNBS can be uptaken by cancer cells after which the cage group is selectively removed by the intracellular GSH, resulting in the generation of SO2 for gas therapy. The reaction also releases the activated photosensitizer, CyI‐OH, that can produce singlet oxygen (1O2) under red light irradiation. Therefore, CyI‐DNBS targets cancer cells for both photodynamic and SO2 gas therapy treatments. The activatable photosensitizer provides a new approach for PDT and SO2 gas synergistic therapy and demonstrates excellent anticancer effect in vivo.
A photosensitizer CyI‐DNBS is reported which releases SO2 via glutathione activation for gas therapy. Meanwhile, the activated photosensitizer is capable of producing cytotoxic 1O2 for photodynamic therapy (PDT) under red light irradiation. CyI‐DNBS has demonstrated highly effective therapeutic effects and can significantly inhibit the tumor growth in vivo, providing a new platform for combined PDT and gas therapy. |
doi_str_mv | 10.1002/adhm.202102017 |
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A photosensitizer CyI‐DNBS is reported which releases SO2 via glutathione activation for gas therapy. Meanwhile, the activated photosensitizer is capable of producing cytotoxic 1O2 for photodynamic therapy (PDT) under red light irradiation. CyI‐DNBS has demonstrated highly effective therapeutic effects and can significantly inhibit the tumor growth in vivo, providing a new platform for combined PDT and gas therapy.</description><identifier>ISSN: 2192-2640</identifier><identifier>EISSN: 2192-2659</identifier><identifier>DOI: 10.1002/adhm.202102017</identifier><identifier>PMID: 34812594</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>activatable photosensitizer ; Anticancer properties ; Cages ; Cancer ; Cancer therapies ; Cell Line, Tumor ; gas therapy ; Glutathione ; Light irradiation ; mitochondria‐targeting ; Photochemotherapy - methods ; Photodynamic therapy ; Photosensitizing Agents - pharmacology ; Photosensitizing Agents - therapeutic use ; Radiation ; red‐light therapy ; Selectivity ; Singlet Oxygen ; Tumor cells ; Tumors</subject><ispartof>Advanced healthcare materials, 2022-02, Vol.11 (4), p.e2102017-n/a</ispartof><rights>2021 Wiley‐VCH GmbH</rights><rights>2021 Wiley-VCH GmbH.</rights><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3737-9e460d4607cb926f870cf884c95902a5d9901c1adb92a9495132be52d702deb73</citedby><cites>FETCH-LOGICAL-c3737-9e460d4607cb926f870cf884c95902a5d9901c1adb92a9495132be52d702deb73</cites><orcidid>0000-0002-8806-322X ; 0000-0001-7777-079X ; 0000-0003-4962-5186 ; 0000-0003-4316-5350</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34812594$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Ran</creatorcontrib><creatorcontrib>Xia, Xiang</creatorcontrib><creatorcontrib>Yang, Yanjun</creatorcontrib><creatorcontrib>Rong, Xiang</creatorcontrib><creatorcontrib>Liu, Ting</creatorcontrib><creatorcontrib>Su, Zehou</creatorcontrib><creatorcontrib>Zeng, Xiaolong</creatorcontrib><creatorcontrib>Du, Jianjun</creatorcontrib><creatorcontrib>Fan, Jiangli</creatorcontrib><creatorcontrib>Sun, Wen</creatorcontrib><creatorcontrib>Peng, Xiaojun</creatorcontrib><title>A Glutathione Activatable Photosensitizer for Combined Photodynamic and Gas Therapy under Red Light Irradiation</title><title>Advanced healthcare materials</title><addtitle>Adv Healthc Mater</addtitle><description>Although photodynamic therapy (PDT) is a promising approach for cancer therapy, most existing photosensitizers lack selectivity for tumor cells and the overexpressed glutathione (GSH) in tumor cells reduces the PDT efficiency. Therefore, designing photosensitizers that can be selectively activated within tumor cells and combine PDT with other therapeutic modalities represents a route for precise and efficient anticancer treatment. Herein, an organic activatable photosensitizer, CyI‐DNBS, bearing 2,4‐dinitrobenzenesulfonate (DNBS) as the cage group is reported. CyI‐DNBS can be uptaken by cancer cells after which the cage group is selectively removed by the intracellular GSH, resulting in the generation of SO2 for gas therapy. The reaction also releases the activated photosensitizer, CyI‐OH, that can produce singlet oxygen (1O2) under red light irradiation. Therefore, CyI‐DNBS targets cancer cells for both photodynamic and SO2 gas therapy treatments. The activatable photosensitizer provides a new approach for PDT and SO2 gas synergistic therapy and demonstrates excellent anticancer effect in vivo.
A photosensitizer CyI‐DNBS is reported which releases SO2 via glutathione activation for gas therapy. Meanwhile, the activated photosensitizer is capable of producing cytotoxic 1O2 for photodynamic therapy (PDT) under red light irradiation. CyI‐DNBS has demonstrated highly effective therapeutic effects and can significantly inhibit the tumor growth in vivo, providing a new platform for combined PDT and gas therapy.</description><subject>activatable photosensitizer</subject><subject>Anticancer properties</subject><subject>Cages</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cell Line, Tumor</subject><subject>gas therapy</subject><subject>Glutathione</subject><subject>Light irradiation</subject><subject>mitochondria‐targeting</subject><subject>Photochemotherapy - methods</subject><subject>Photodynamic therapy</subject><subject>Photosensitizing Agents - pharmacology</subject><subject>Photosensitizing Agents - therapeutic use</subject><subject>Radiation</subject><subject>red‐light therapy</subject><subject>Selectivity</subject><subject>Singlet Oxygen</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>2192-2640</issn><issn>2192-2659</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqF0c9LwzAYBuAgihtzV48S8OJlM0l_5limboOJIvNc0iS1GW0zk1SZf70ZnRO8GAgJfE_ehHwAXGI0xQiRWyaqZkoQwYggnJyAIcGUTEgc0dPjPkQDMLZ2g_yIIxyn-BwMgjDFJKLhEOgMzuvOMVcp3UqYcac-mGNFLeFzpZ22srXKqS9pYKkNnOmmUK0UfVHsWtYoDlkr4JxZuK6kYdsd7Frh_YtnK_VWObg0hgnFnL_iApyVrLZyfFhH4PXhfj1bTFZP8-UsW014kATJhMowRsLPhBeUxGWaIF6machpRBFhkaAUYY6Z8FVGQxrhgBQyIiJBRMgiCUbgps_dGv3eSevyRlku65q1Unc2JzHCYUoCuqfXf-hGd6b1r_OKpDRBFAdeTXvFjbbWyDLfGtUws8sxyvfdyPfdyI_d8AeuDrFd0Uhx5D9_7wHtwaeq5e6fuDy7Wzz-hn8DuEWVbg</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Wang, Ran</creator><creator>Xia, Xiang</creator><creator>Yang, Yanjun</creator><creator>Rong, Xiang</creator><creator>Liu, Ting</creator><creator>Su, Zehou</creator><creator>Zeng, Xiaolong</creator><creator>Du, Jianjun</creator><creator>Fan, Jiangli</creator><creator>Sun, Wen</creator><creator>Peng, Xiaojun</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T5</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7TO</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8806-322X</orcidid><orcidid>https://orcid.org/0000-0001-7777-079X</orcidid><orcidid>https://orcid.org/0000-0003-4962-5186</orcidid><orcidid>https://orcid.org/0000-0003-4316-5350</orcidid></search><sort><creationdate>20220201</creationdate><title>A Glutathione Activatable Photosensitizer for Combined Photodynamic and Gas Therapy under Red Light Irradiation</title><author>Wang, Ran ; 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Therefore, designing photosensitizers that can be selectively activated within tumor cells and combine PDT with other therapeutic modalities represents a route for precise and efficient anticancer treatment. Herein, an organic activatable photosensitizer, CyI‐DNBS, bearing 2,4‐dinitrobenzenesulfonate (DNBS) as the cage group is reported. CyI‐DNBS can be uptaken by cancer cells after which the cage group is selectively removed by the intracellular GSH, resulting in the generation of SO2 for gas therapy. The reaction also releases the activated photosensitizer, CyI‐OH, that can produce singlet oxygen (1O2) under red light irradiation. Therefore, CyI‐DNBS targets cancer cells for both photodynamic and SO2 gas therapy treatments. The activatable photosensitizer provides a new approach for PDT and SO2 gas synergistic therapy and demonstrates excellent anticancer effect in vivo.
A photosensitizer CyI‐DNBS is reported which releases SO2 via glutathione activation for gas therapy. Meanwhile, the activated photosensitizer is capable of producing cytotoxic 1O2 for photodynamic therapy (PDT) under red light irradiation. CyI‐DNBS has demonstrated highly effective therapeutic effects and can significantly inhibit the tumor growth in vivo, providing a new platform for combined PDT and gas therapy.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34812594</pmid><doi>10.1002/adhm.202102017</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-8806-322X</orcidid><orcidid>https://orcid.org/0000-0001-7777-079X</orcidid><orcidid>https://orcid.org/0000-0003-4962-5186</orcidid><orcidid>https://orcid.org/0000-0003-4316-5350</orcidid></addata></record> |
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subjects | activatable photosensitizer Anticancer properties Cages Cancer Cancer therapies Cell Line, Tumor gas therapy Glutathione Light irradiation mitochondria‐targeting Photochemotherapy - methods Photodynamic therapy Photosensitizing Agents - pharmacology Photosensitizing Agents - therapeutic use Radiation red‐light therapy Selectivity Singlet Oxygen Tumor cells Tumors |
title | A Glutathione Activatable Photosensitizer for Combined Photodynamic and Gas Therapy under Red Light Irradiation |
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