Inducing tumor ferroptosis a pH-responsive NIR-II photothermal agent initiating lysosomal dysfunction
Ferroptosis is a unique programmed cell death process that was discovered a few years ago and plays an important role in tumor biology and treatment. However, it still remains a challenge to modulate tumor ferroptosis by spatiotemporally controlled cell-intrinsic Fenton chemistry. Herein, a pH activ...
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Veröffentlicht in: | Nanoscale 2023-12, Vol.15 (47), p.1974-1978 |
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container_end_page | 1978 |
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container_issue | 47 |
container_start_page | 1974 |
container_title | Nanoscale |
container_volume | 15 |
creator | Zhang, Zhiwei Xiang, Jingjing Guan, Lijiao Chen, Pu Li, Changzhong Guo, Chunlei Hu, Yan Huang, Saipeng Cai, Lintao Gong, Ping |
description | Ferroptosis is a unique programmed cell death process that was discovered a few years ago and plays an important role in tumor biology and treatment. However, it still remains a challenge to modulate tumor ferroptosis by spatiotemporally controlled cell-intrinsic Fenton chemistry. Herein, a pH activated photothermal sensitizer IR-PE has been designed and synthesized on the basis of cyanine bearing a diamine moiety, which is capable of triggering the lysosomal dysfunction-mediated Fenton pathway under the irradiation of near-infrared light to evoke ferroptosis, thereby improving antitumor efficacy and mitigating systemic side effects.
A pH-responsive molecule that can promote the intrinsic Fenton reaction in tumor cells with NIR light irradiation was developed, and the acid-activatable photothermal properties of IR-PE also exhibited strong antitumor efficacy. |
doi_str_mv | 10.1039/d3nr04124g |
format | Article |
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A pH-responsive molecule that can promote the intrinsic Fenton reaction in tumor cells with NIR light irradiation was developed, and the acid-activatable photothermal properties of IR-PE also exhibited strong antitumor efficacy.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/d3nr04124g</identifier><ispartof>Nanoscale, 2023-12, Vol.15 (47), p.1974-1978</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Zhang, Zhiwei</creatorcontrib><creatorcontrib>Xiang, Jingjing</creatorcontrib><creatorcontrib>Guan, Lijiao</creatorcontrib><creatorcontrib>Chen, Pu</creatorcontrib><creatorcontrib>Li, Changzhong</creatorcontrib><creatorcontrib>Guo, Chunlei</creatorcontrib><creatorcontrib>Hu, Yan</creatorcontrib><creatorcontrib>Huang, Saipeng</creatorcontrib><creatorcontrib>Cai, Lintao</creatorcontrib><creatorcontrib>Gong, Ping</creatorcontrib><title>Inducing tumor ferroptosis a pH-responsive NIR-II photothermal agent initiating lysosomal dysfunction</title><title>Nanoscale</title><description>Ferroptosis is a unique programmed cell death process that was discovered a few years ago and plays an important role in tumor biology and treatment. However, it still remains a challenge to modulate tumor ferroptosis by spatiotemporally controlled cell-intrinsic Fenton chemistry. Herein, a pH activated photothermal sensitizer IR-PE has been designed and synthesized on the basis of cyanine bearing a diamine moiety, which is capable of triggering the lysosomal dysfunction-mediated Fenton pathway under the irradiation of near-infrared light to evoke ferroptosis, thereby improving antitumor efficacy and mitigating systemic side effects.
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A pH-responsive molecule that can promote the intrinsic Fenton reaction in tumor cells with NIR light irradiation was developed, and the acid-activatable photothermal properties of IR-PE also exhibited strong antitumor efficacy.</abstract><doi>10.1039/d3nr04124g</doi><tpages>5</tpages></addata></record> |
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title | Inducing tumor ferroptosis a pH-responsive NIR-II photothermal agent initiating lysosomal dysfunction |
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