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Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy

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 nanoaggreg...

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Autores principales: Chen, Jia, Li, Shengke, Wang, Zeyu, Pan, Yating, Wei, Jianwen, Lu, Siyu, Zhang, Qing-Wen, Wang, Lian-Hui, Wang, Ruibing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188462/
https://www.ncbi.nlm.nih.gov/pubmed/34168825
http://dx.doi.org/10.1039/d1sc01139a
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author Chen, Jia
Li, Shengke
Wang, Zeyu
Pan, Yating
Wei, Jianwen
Lu, Siyu
Zhang, Qing-Wen
Wang, Lian-Hui
Wang, Ruibing
author_facet Chen, Jia
Li, Shengke
Wang, Zeyu
Pan, Yating
Wei, Jianwen
Lu, Siyu
Zhang, Qing-Wen
Wang, Lian-Hui
Wang, Ruibing
author_sort Chen, Jia
collection PubMed
description 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.
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spelling pubmed-81884622021-06-23 Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy Chen, Jia Li, Shengke Wang, Zeyu Pan, Yating Wei, Jianwen Lu, Siyu Zhang, Qing-Wen Wang, Lian-Hui Wang, Ruibing Chem Sci Chemistry 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. The Royal Society of Chemistry 2021-04-21 /pmc/articles/PMC8188462/ /pubmed/34168825 http://dx.doi.org/10.1039/d1sc01139a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Chen, Jia
Li, Shengke
Wang, Zeyu
Pan, Yating
Wei, Jianwen
Lu, Siyu
Zhang, Qing-Wen
Wang, Lian-Hui
Wang, Ruibing
Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
title Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
title_full Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
title_fullStr Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
title_full_unstemmed Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
title_short Synthesis of an AIEgen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
title_sort synthesis of an aiegen functionalized cucurbit[7]uril for subcellular bioimaging and synergistic photodynamic therapy and supramolecular chemotherapy
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188462/
https://www.ncbi.nlm.nih.gov/pubmed/34168825
http://dx.doi.org/10.1039/d1sc01139a
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