Serveur d'exploration sur les relations entre la France et l'Australie

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Assembly and Degradation of Low‐Fouling Click‐Functionalized Poly(ethylene glycol)‐Based Multilayer Films and Capsules

Identifieur interne : 006491 ( Main/Exploration ); précédent : 006490; suivant : 006492

Assembly and Degradation of Low‐Fouling Click‐Functionalized Poly(ethylene glycol)‐Based Multilayer Films and Capsules

Auteurs : Melissa K. M. Leung [Australie] ; Georgina K. Such [Australie] ; Angus P. R. Johnston [Australie] ; Dhee P. Biswas [Australie] ; Zhiyuan Zhu [Australie] ; Yan Yan [Australie] ; Jean-François Lutz [Allemagne, France] ; Frank Caruso [Australie]

Source :

RBID : ISTEX:8F8C8E132096B09EBB125ED03C5906F39914115D

Descripteurs français

English descriptors

Abstract

Nano‐/micrometer‐scaled films and capsules made of low‐fouling materials such as poly(ethylene glycol) (PEG) are of interest for drug delivery and tissue engineering applications. Herein, the assembly and degradation of low‐fouling, alkyne‐functionalized PEG (PEGAlk) multilayer films and capsules, which are prepared by combining layer‐by‐layer (LbL) assembly and click chemistry, are reported. A nonlinear, temperature‐responsive PEGAlk is synthesized, and is then used to form hydrogen‐bonded multilayers with poly(methacrylic acid) (PMA) at pH 5. The thermoresponsive behavior of PEGAlk is exploited to tailor film buildup by adjusting the assembly conditions. Using alkyne–azide click chemistry, PEGAlk/PMA multilayers are crosslinked with a bisazide linker that contains a disulfide bond, rendering these films and capsules redox‐responsive. At pH 7, by disrupting the hydrogen bonding between the polymers, PEGAlk LbL films and PEGAlk‐based capsules are obtained. These films exhibit specific deconstruction properties under simulated intracellular reducing conditions, but remain stable at physiological pH, suggesting potential applications in controlled drug release. The low‐fouling properties of the PEG films are confirmed by incubation with human serum and a blood clot. Additionally, these capsules showed negligible toxicity to human cells.

Url:
DOI: 10.1002/smll.201002258


Affiliations:


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Le document en format XML

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<term>Adsorption</term>
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<term>Bisazide</term>
<term>Bisazide linker</term>
<term>Buildup</term>
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<term>Click</term>
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<term>Frequency change</term>
<term>Full papers</term>
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<term>Thermoresponsive behavior</term>
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<term>Triethylene glycol</term>
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<term>Frequency change</term>
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<div type="abstract" xml:lang="en">Nano‐/micrometer‐scaled films and capsules made of low‐fouling materials such as poly(ethylene glycol) (PEG) are of interest for drug delivery and tissue engineering applications. Herein, the assembly and degradation of low‐fouling, alkyne‐functionalized PEG (PEGAlk) multilayer films and capsules, which are prepared by combining layer‐by‐layer (LbL) assembly and click chemistry, are reported. A nonlinear, temperature‐responsive PEGAlk is synthesized, and is then used to form hydrogen‐bonded multilayers with poly(methacrylic acid) (PMA) at pH 5. The thermoresponsive behavior of PEGAlk is exploited to tailor film buildup by adjusting the assembly conditions. Using alkyne–azide click chemistry, PEGAlk/PMA multilayers are crosslinked with a bisazide linker that contains a disulfide bond, rendering these films and capsules redox‐responsive. At pH 7, by disrupting the hydrogen bonding between the polymers, PEGAlk LbL films and PEGAlk‐based capsules are obtained. These films exhibit specific deconstruction properties under simulated intracellular reducing conditions, but remain stable at physiological pH, suggesting potential applications in controlled drug release. The low‐fouling properties of the PEG films are confirmed by incubation with human serum and a blood clot. Additionally, these capsules showed negligible toxicity to human cells.</div>
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