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231225s2020 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202004385
|2 doi
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|a pubmed24n1481.xml
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|a (DE-627)NLM31732036X
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|a (NLM)33164250
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Shao, Dan
|e verfasserin
|4 aut
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|a Biomimetic Diselenide-Bridged Mesoporous Organosilica Nanoparticles as an X-ray-Responsive Biodegradable Carrier for Chemo-Immunotherapy
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|c 2020
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 24.07.2024
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|a Date Revised 24.07.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2020 Wiley-VCH GmbH.
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|a Chemotherapy causes off-target toxicity and is often ineffective against solid tumors. Targeted and on-demand release of chemotherapeutics remains a challenge. Here, cancer-cell-membrane-coated mesoporous organosilica nanoparticles (MONs) containing X-ray- and reactive oxygen species (ROS)-responsive diselenide bonds for controlled release of doxorubicin (DOX) at tumor sites are developed. DOX-loaded MONs coated with 4T1 breast cancer cell membranes (CMMON@DOX) show greater accumulation at tumor sites and prolonged blood circulation time versus an uncoated control in mice bearing 4T1 orthotopic mammary tumors. Under low-dose X-ray radiation, the DOX-loaded MONs exhibit carrier degradation-controlled release via cleavage of diselenide bonds, resulting in DOX-mediated immunogenic cell death at the tumor site. Combination with a PD-L1 checkpoint blockade further enhances inhibition of tumor growth and metastasis with low systemic toxicity. Together, the findings show the promise of these biomimetic, radiation-responsive diselenide-bond-bridged MONs in chemo-immunotherapy
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|a Journal Article
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|a X-ray radiation responsivity
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|a biodegradable mesoporous organosilica nanoparticles
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|a biomimetic
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|a chemo-immunotherapy
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|a diselenide bonds
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|a Doxorubicin
|2 NLM
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|a 80168379AG
|2 NLM
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|a Drug Carriers
|2 NLM
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|a Reactive Oxygen Species
|2 NLM
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|a Organosilicon Compounds
|2 NLM
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|a Organoselenium Compounds
|2 NLM
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|a Zhang, Fan
|e verfasserin
|4 aut
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|a Chen, Fangman
|e verfasserin
|4 aut
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|a Zheng, Xiao
|e verfasserin
|4 aut
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|a Hu, Hanze
|e verfasserin
|4 aut
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|a Yang, Chao
|e verfasserin
|4 aut
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1 |
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|a Tu, Zhaoxu
|e verfasserin
|4 aut
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1 |
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|a Wang, Zheng
|e verfasserin
|4 aut
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1 |
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|a Chang, Zhimin
|e verfasserin
|4 aut
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|a Lu, Junna
|e verfasserin
|4 aut
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|a Li, Tianyu
|e verfasserin
|4 aut
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1 |
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|a Zhang, Yuan
|e verfasserin
|4 aut
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|a Chen, Li
|e verfasserin
|4 aut
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|a Leong, Kam W
|e verfasserin
|4 aut
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|a Dong, Wen-Fei
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 32(2020), 50 vom: 01. Dez., Seite e2004385
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
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|g volume:32
|g year:2020
|g number:50
|g day:01
|g month:12
|g pages:e2004385
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|u http://dx.doi.org/10.1002/adma.202004385
|3 Volltext
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|a AR
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|d 32
|j 2020
|e 50
|b 01
|c 12
|h e2004385
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