Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle

Abstract Ionizable cyclodextrins have attracted increasing attention in host–guest chemistry and pharmaceutical industry, mainly due to the introduction of favorable electrostatic interactions. The ionizable cyclodextrins could not only enhance its own solubility but also induce oppositely charged g...

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Autores principales: He-Lue Sun, Ying-Ming Zhang, Yong Chen, Yu Liu
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Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/8c4b25b6f06d49c7a341c3cad5423a47
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spelling oai:doaj.org-article:8c4b25b6f06d49c7a341c3cad5423a472021-12-02T16:08:01ZPolyanionic Cyclodextrin Induced Supramolecular Nanoparticle10.1038/s41598-016-0026-z2045-2322https://doaj.org/article/8c4b25b6f06d49c7a341c3cad5423a472016-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-016-0026-zhttps://doaj.org/toc/2045-2322Abstract Ionizable cyclodextrins have attracted increasing attention in host–guest chemistry and pharmaceutical industry, mainly due to the introduction of favorable electrostatic interactions. The ionizable cyclodextrins could not only enhance its own solubility but also induce oppositely charged guests to form more stable complex. However, the aggregation induced by charged cyclodextrins has rarely been reported. In this work, guided by the concept of molecular-induced aggregation, a series of carboxyl modified cyclodextrins were synthesized via “click” and hydrolysis reaction. Then, UV-vis spectrum was used to investigate the aggregating behaviors induced by these cyclodextrins towards the cationic guest molecules. The results showed that only the hepta-carboxyl-β-cyclodextrin could induce the guest molecules to self-assemble into supramolecular spherical nanoparticles. Meanwhile, it could form stable inclusion complex with amantadine, a drug for anti-Parkinson and antiviral. The assembly behaviors were investigated by dynamic light scattering, scanning electron microscope, atomic force microscope, transmission electron microscope and NMR spectroscopy. The supramolecular nanoparticles induced by hepta-carboxyl-β-CD and its inclusion with amantadine could be used to encapsulate the model drug and achieve its controlled releasing behaviors.He-Lue SunYing-Ming ZhangYong ChenYu LiuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 6, Iss 1, Pp 1-9 (2016)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
He-Lue Sun
Ying-Ming Zhang
Yong Chen
Yu Liu
Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle
description Abstract Ionizable cyclodextrins have attracted increasing attention in host–guest chemistry and pharmaceutical industry, mainly due to the introduction of favorable electrostatic interactions. The ionizable cyclodextrins could not only enhance its own solubility but also induce oppositely charged guests to form more stable complex. However, the aggregation induced by charged cyclodextrins has rarely been reported. In this work, guided by the concept of molecular-induced aggregation, a series of carboxyl modified cyclodextrins were synthesized via “click” and hydrolysis reaction. Then, UV-vis spectrum was used to investigate the aggregating behaviors induced by these cyclodextrins towards the cationic guest molecules. The results showed that only the hepta-carboxyl-β-cyclodextrin could induce the guest molecules to self-assemble into supramolecular spherical nanoparticles. Meanwhile, it could form stable inclusion complex with amantadine, a drug for anti-Parkinson and antiviral. The assembly behaviors were investigated by dynamic light scattering, scanning electron microscope, atomic force microscope, transmission electron microscope and NMR spectroscopy. The supramolecular nanoparticles induced by hepta-carboxyl-β-CD and its inclusion with amantadine could be used to encapsulate the model drug and achieve its controlled releasing behaviors.
format article
author He-Lue Sun
Ying-Ming Zhang
Yong Chen
Yu Liu
author_facet He-Lue Sun
Ying-Ming Zhang
Yong Chen
Yu Liu
author_sort He-Lue Sun
title Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle
title_short Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle
title_full Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle
title_fullStr Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle
title_full_unstemmed Polyanionic Cyclodextrin Induced Supramolecular Nanoparticle
title_sort polyanionic cyclodextrin induced supramolecular nanoparticle
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/8c4b25b6f06d49c7a341c3cad5423a47
work_keys_str_mv AT heluesun polyanioniccyclodextrininducedsupramolecularnanoparticle
AT yingmingzhang polyanioniccyclodextrininducedsupramolecularnanoparticle
AT yongchen polyanioniccyclodextrininducedsupramolecularnanoparticle
AT yuliu polyanioniccyclodextrininducedsupramolecularnanoparticle
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