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Merck

Protease-degradable electrospun fibrous hydrogels.

Nature communications (2015-03-24)
Ryan J Wade, Ethan J Bassin, Christopher B Rodell, Jason A Burdick
要旨

Electrospun nanofibres are promising in biomedical applications to replicate features of the natural extracellular matrix (ECM). However, nearly all electrospun scaffolds are either non-degradable or degrade hydrolytically, whereas natural ECM degrades proteolytically, often through matrix metalloproteinases. Here we synthesize reactive macromers that contain protease-cleavable and fluorescent peptides and are able to form both isotropic hydrogels and electrospun fibrous hydrogels through a photoinitiated polymerization. These biomimetic scaffolds are susceptible to protease-mediated cleavage in vitro in a protease dose-dependent manner and in vivo in a subcutaneous mouse model using transdermal fluorescent imaging to monitor degradation. Importantly, materials containing an alternate and non-protease-cleavable peptide sequence are stable in both in vitro and in vivo settings. To illustrate the specificity in degradation, scaffolds with mixed fibre populations support selective fibre degradation based on individual fibre degradability. Overall, this represents a novel biomimetic approach to generate protease-sensitive fibrous scaffolds for biomedical applications.

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Sigma-Aldrich
ジメチルスルホキシド, Hybri-Max, sterile-filtered, BioReagent, suitable for hybridoma, ≥99.7%
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アセトン, ACS reagent, ≥99.5%
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ジメチルスルホキシド, ACS reagent, ≥99.9%
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ジメチルスルホキシド, for molecular biology
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アセトン, suitable for HPLC, ≥99.9%
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ジメチルスルホキシド, suitable for HPLC, ≥99.7%
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N,N-ジメチルホルムアミド, ACS reagent, ≥99.8%
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ジメチルスルホキシド, sterile-filtered, BioPerformance Certified, meets EP, USP testing specifications, suitable for hybridoma
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N,N-ジメチルホルムアミド, suitable for HPLC, ≥99.9%
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アセトン, HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%
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