Residential College | false |
Status | 已發表Published |
Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy | |
Chen, Jia1; Li, Shengke2,3; Wang, Zeyu1; Pan, Yating3; Wei, Jianwen1; Lu, Siyu4; Zhang, Qing Wen1; Wang, Lian Hui3; Wang, Ruibing1 | |
2021-04-21 | |
Source Publication | Chemical Science |
ISSN | 2041-6520 |
Volume | 12Issue:22Pages:7727-7734 |
Abstract | Aggregation-induced emission (AIE) based fluorophores (AIEgens) have attracted increasing attention for biomedical applications due to their unique optical properties. Here we report an AIE photosensitizer functionalized CB[7], namely AIECB[7], which could spontaneously self-assemble into nanoaggregates in aqueous solutions. Interestingly, the carbonyl-lace of CB[7] may potentially act as a proton acceptor in an acidic environment to fine-tune the fluorescence and singlet oxygen generation of AIECB[7] nanoaggregates by regulating the inner stacking of AIEgens. Additionally, benefiting from the guest-binding properties of CB[7], oxaliplatin was included into AIECB[7] nanoaggregates for combined photodynamic therapy and supramolecular chemotherapy. To show the modular versatility of this supramolecular system, a hypoxia-activatable prodrug banoxantrone (AQ4N) was loaded into AIECB[7] nanoaggregates, which exhibited synergistic antitumor effects on a multicellular tumor spheroid model (MCTS). This work not only provides AIECB[7] for versatile theranostic applications, but also offers important new insights into the design and development of macrocycle-conjugated AIE materials for diverse biomedical applications. |
DOI | 10.1039/d1sc01139a |
URL | View the original |
Indexed By | SCIE ; IC |
Language | 英語English |
WOS Research Area | Chemistry |
WOS Subject | Chemistry, Multidisciplinary |
WOS ID | WOS:000649315900001 |
Publisher | Royal Society of Chemistry |
Scopus ID | 2-s2.0-85107736632 |
Fulltext Access | |
Citation statistics | |
Document Type | Journal article |
Collection | DEPARTMENT OF PHARMACEUTICAL SCIENCES Faculty of Health Sciences Institute of Chinese Medical Sciences THE STATE KEY LABORATORY OF QUALITY RESEARCH IN CHINESE MEDICINE (UNIVERSITY OF MACAU) |
Corresponding Author | Wang, Ruibing |
Affiliation | 1.State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Taipa, 999078, Macao 2.School of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China 3.Key Laboratory for Organic Electronics and Information Displays, Institute of Advanced Materials, Nanjing University of Posts and Telecommunications, Nanjing, 9 Wenyuan Road, 210023, China 4.Green Catalysis Center, College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou, 100 Kexue Road, 450001, China |
First Author Affilication | Institute of Chinese Medical Sciences |
Corresponding Author Affilication | Institute of Chinese Medical Sciences |
Recommended Citation GB/T 7714 | Chen, Jia,Li, Shengke,Wang, Zeyu,et al. Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy[J]. Chemical Science, 2021, 12(22), 7727-7734. |
APA | Chen, Jia., Li, Shengke., Wang, Zeyu., Pan, Yating., Wei, Jianwen., Lu, Siyu., Zhang, Qing Wen., Wang, Lian Hui., & Wang, Ruibing (2021). Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy. Chemical Science, 12(22), 7727-7734. |
MLA | Chen, Jia,et al."Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy".Chemical Science 12.22(2021):7727-7734. |
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