Tumor microenvironment-activatable boolean logic supramolecular nanotheranostics based on a pillar[6]arene for tumor hypoxia imaging and multimodal synergistic therapy
Xin Liu
1, 2, 3, 4, 5, 6
,
Meng Chi
1
,
Meng Chi
1, 2, 3, 4, 5, 6
,
Guiqing Ji
4, 5, 6, 7, 8
,
Ji Liu
1, 2, 3, 4, 5, 6
,
Peng Zhu
1, 2, 3, 4, 5, 6
,
Jianqiang Qian
1, 2, 3, 4, 5, 6
,
Shun Xing Zhu
9
,
Shun-Xing Zhu
4, 5, 6, 9, 10
,
Yanan Zhang
1, 2, 3, 4, 5, 6
,
Yong Ling
1, 2, 3, 4, 5, 6
2
School of Pharmacy
3
Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target
5
Nantong 226001
|
6
P. R. China
|
8
Key Laboratory of Neuroregeneration
Publication type: Journal Article
Publication date: 2021-06-09
scimago Q1
wos Q1
SJR: 1.444
CiteScore: 13.2
Impact factor: 6.4
ISSN: 20521537
Materials Chemistry
General Materials Science
Abstract
Supramolecular construction of nanotheranostics is a highly challenging and demanding task for tumor precision diagnosis and therapy. In this study, inspired by specific microenvironments and the abnormal metabolic path of tumors, we skillfully integrated hypoxia-responsive fluorescence imaging, cancer starvation therapy, oxidative therapy, and chemotherapy to fabricate supramolecular nanotheranostics (GOx@NPs) through host–guest interactions between a carboxylated-pillar[6]arene (WP6) host and a prodrug guest (Azo-G). Depending on the excellent responsive ability to hypoxia, esterase and pH which are signature features of the tumor microenvironment, GOx@NPs could not only realize selective fluorescence imaging and diagnosis against tumor hypoxia but also possess remarkable synergistic treatment effects of starving therapy, oxidative therapy, and chemotherapy on cancer cells in vitro and in vivo. Furthermore, we developed a two-layer cascade logic gate based on GOx@NPs to perform intracellular logic operations with cancer endogenous inputs for biocomputing. This study provides a referential example to develop intelligent tumor microenvironment-responsive supramolecular nanosystems with the ability of logical computing for precision cancer diagnosis and synergistic therapy.
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Liu X. et al. Tumor microenvironment-activatable boolean logic supramolecular nanotheranostics based on a pillar[6]arene for tumor hypoxia imaging and multimodal synergistic therapy // Materials Chemistry Frontiers. 2021. Vol. 5. No. 15. pp. 5846-5856.
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Liu X. et al. Tumor microenvironment-activatable boolean logic supramolecular nanotheranostics based on a pillar[6]arene for tumor hypoxia imaging and multimodal synergistic therapy // Materials Chemistry Frontiers. 2021. Vol. 5. No. 15. pp. 5846-5856.
Cite this
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TY - JOUR
DO - 10.1039/d1qm00411e
UR - https://xlink.rsc.org/?DOI=D1QM00411E
TI - Tumor microenvironment-activatable boolean logic supramolecular nanotheranostics based on a pillar[6]arene for tumor hypoxia imaging and multimodal synergistic therapy
T2 - Materials Chemistry Frontiers
AU - Liu, Xin
AU - Chi, Meng
AU - Meng Chi
AU - Ji, Guiqing
AU - Liu, Ji
AU - Zhu, Peng
AU - Qian, Jianqiang
AU - Zhu, Shun Xing
AU - Zhu, Shun-Xing
AU - Zhang, Yanan
AU - Ling, Yong
PY - 2021
DA - 2021/06/09
PB - Royal Society of Chemistry (RSC)
SP - 5846-5856
IS - 15
VL - 5
SN - 2052-1537
ER -
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@article{2021_Liu,
author = {Xin Liu and Meng Chi and Meng Chi and Guiqing Ji and Ji Liu and Peng Zhu and Jianqiang Qian and Shun Xing Zhu and Shun-Xing Zhu and Yanan Zhang and Yong Ling and others},
title = {Tumor microenvironment-activatable boolean logic supramolecular nanotheranostics based on a pillar[6]arene for tumor hypoxia imaging and multimodal synergistic therapy},
journal = {Materials Chemistry Frontiers},
year = {2021},
volume = {5},
publisher = {Royal Society of Chemistry (RSC)},
month = {jun},
url = {https://xlink.rsc.org/?DOI=D1QM00411E},
number = {15},
pages = {5846--5856},
doi = {10.1039/d1qm00411e}
}
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Liu, Xin, et al. “Tumor microenvironment-activatable boolean logic supramolecular nanotheranostics based on a pillar[6]arene for tumor hypoxia imaging and multimodal synergistic therapy.” Materials Chemistry Frontiers, vol. 5, no. 15, Jun. 2021, pp. 5846-5856. https://xlink.rsc.org/?DOI=D1QM00411E.