Supramolecular nanoparticles constructed from pillar[5]arene-based host-guest complexation with enhanced aggregation-induced emission for imaging-guided drug delivery

Fluorophores with aggregation-induced emission (AIE) characteristics have attracted more and more attention due to their unparalleled advantages in terms of sensitivity and photostability, and have been extensively utilized for disease diagnosis and therapy. However, it remains challenging to restri...

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Veröffentlicht in:Materials chemistry frontiers 2021-02, Vol.5 (3), p.1418-1427
Hauptverfasser: Liu, Dahai, Du, Jianshi, Qi, Shaolong, Li, Mengyao, Wang, Jianfeng, Liu, Meihan, Du, Xianlong, Wang, Xinyu, Ren, Bichen, Wu, Dan, Shen, Jie
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container_issue 3
container_start_page 1418
container_title Materials chemistry frontiers
container_volume 5
creator Liu, Dahai
Du, Jianshi
Qi, Shaolong
Li, Mengyao
Wang, Jianfeng
Liu, Meihan
Du, Xianlong
Wang, Xinyu
Ren, Bichen
Wu, Dan
Shen, Jie
description Fluorophores with aggregation-induced emission (AIE) characteristics have attracted more and more attention due to their unparalleled advantages in terms of sensitivity and photostability, and have been extensively utilized for disease diagnosis and therapy. However, it remains challenging to restrict the intramolecular rotation of the AIE luminogens (AIEgens) both in solution and aggregated states. Herein, we utilize host-guest chemistry to achieve this meaningful goal by using a carboxylate-modified pillar[5]arene H as a supramolecular host and an AIEgen containing a tetraphenylethene core G as a guest. The AIE effect of the fluorophore is effectively enhanced upon the formation of an inclusion host-guest complex H ⊃ G , and the fluorescence of H ⊃ G is much more intensive than that of free G . Supramolecular nanoparticles ( SNPs ) with high emission are prepared from H ⊃ G using a nanoprecipitation method, which can be used as a fluorescent probe for living cell imaging showing superior photostability against laser excitation. Intriguingly, the formed SNPs act as nanocarriers to encapsulate doxorubicin (DOX) to deactivate both the fluorescence of SNPs and DOX caused by the energy transfer relay (ETR) effect, which is mediated by Förster resonance energy transfer and aggregation-caused quenching. The release of loaded DOX after cellular internalization interrupts the ETR effect to light up the silenced fluorescence, thus allowing in situ visualization of drug release. More importantly, the anticancer efficacy of the loaded drug is greatly maintained using this sophisticated supramolecular system, showing promising potential in imaging-guided drug delivery. Supramolecular nanoparticles with enhanced aggregation-induced emission are prepared by taking advantage of pillar[5]arene-based host-guest complexation, and are sophisticated nanocarriers for imaging-guided drug delivery.
doi_str_mv 10.1039/d0qm00974a
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However, it remains challenging to restrict the intramolecular rotation of the AIE luminogens (AIEgens) both in solution and aggregated states. Herein, we utilize host-guest chemistry to achieve this meaningful goal by using a carboxylate-modified pillar[5]arene H as a supramolecular host and an AIEgen containing a tetraphenylethene core G as a guest. The AIE effect of the fluorophore is effectively enhanced upon the formation of an inclusion host-guest complex H ⊃ G , and the fluorescence of H ⊃ G is much more intensive than that of free G . Supramolecular nanoparticles ( SNPs ) with high emission are prepared from H ⊃ G using a nanoprecipitation method, which can be used as a fluorescent probe for living cell imaging showing superior photostability against laser excitation. Intriguingly, the formed SNPs act as nanocarriers to encapsulate doxorubicin (DOX) to deactivate both the fluorescence of SNPs and DOX caused by the energy transfer relay (ETR) effect, which is mediated by Förster resonance energy transfer and aggregation-caused quenching. The release of loaded DOX after cellular internalization interrupts the ETR effect to light up the silenced fluorescence, thus allowing in situ visualization of drug release. More importantly, the anticancer efficacy of the loaded drug is greatly maintained using this sophisticated supramolecular system, showing promising potential in imaging-guided drug delivery. 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Intriguingly, the formed SNPs act as nanocarriers to encapsulate doxorubicin (DOX) to deactivate both the fluorescence of SNPs and DOX caused by the energy transfer relay (ETR) effect, which is mediated by Förster resonance energy transfer and aggregation-caused quenching. The release of loaded DOX after cellular internalization interrupts the ETR effect to light up the silenced fluorescence, thus allowing in situ visualization of drug release. More importantly, the anticancer efficacy of the loaded drug is greatly maintained using this sophisticated supramolecular system, showing promising potential in imaging-guided drug delivery. 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Intriguingly, the formed SNPs act as nanocarriers to encapsulate doxorubicin (DOX) to deactivate both the fluorescence of SNPs and DOX caused by the energy transfer relay (ETR) effect, which is mediated by Förster resonance energy transfer and aggregation-caused quenching. The release of loaded DOX after cellular internalization interrupts the ETR effect to light up the silenced fluorescence, thus allowing in situ visualization of drug release. More importantly, the anticancer efficacy of the loaded drug is greatly maintained using this sophisticated supramolecular system, showing promising potential in imaging-guided drug delivery. 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source Royal Society Of Chemistry Journals 2008-
subjects Agglomeration
Anticancer properties
Chemical compounds
Doxorubicin
Emission
Energy transfer
Fluorescent indicators
Medical imaging
Nanoparticles
NMR
Nuclear magnetic resonance
Supramolecular compounds
title Supramolecular nanoparticles constructed from pillar[5]arene-based host-guest complexation with enhanced aggregation-induced emission for imaging-guided drug delivery
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