2020
DOI: 10.1016/j.cej.2020.125964
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S-nitrosated keratin composite mats with NO release capacity for wound healing

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Cited by 64 publications
(59 citation statements)
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“…Hence, we next first evaluated whether Ce6@Arg‐ADP can further generate trace amounts of NO in vivo after exerting its highly efficient antibacterial effect to promote angiogenesis and epithelialization. As the half‐life of NO is extremely short (only 1–5 s) [ 64,65 ] and there are many practical challenges for detecting NO generation in vivo in real‐time, the NO generation behavior was evaluated via an in vitro simulation experiment.…”
Section: Resultsmentioning
confidence: 99%
“…Hence, we next first evaluated whether Ce6@Arg‐ADP can further generate trace amounts of NO in vivo after exerting its highly efficient antibacterial effect to promote angiogenesis and epithelialization. As the half‐life of NO is extremely short (only 1–5 s) [ 64,65 ] and there are many practical challenges for detecting NO generation in vivo in real‐time, the NO generation behavior was evaluated via an in vitro simulation experiment.…”
Section: Resultsmentioning
confidence: 99%
“…Additionally, keratins contain cell adhesion motifs similar in structure to extracellular matrix proteins (such as collagen or fibronectin), arginine-glycine-aspartate (RGD) and leucine-aspartate-valine (LDV), which can support cell attachment and proliferation [ 5 ]. These unique structures and biological properties make keratin the focus of the biomedical field, including wound dressing, tissue engineering and drug delivery [ 6 , 7 , 8 , 9 , 10 , 11 , 12 ]. Nevertheless, the shortcomings of brittleness, poor mechanical properties and processing properties limit the practical use of keratin [ 13 , 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…Nevertheless, the shortcomings of brittleness, poor mechanical properties and processing properties limit the practical use of keratin [ 13 , 14 ]. Synthetic or natural polymers are usually added as plasticizers and crosslinkers to form composite materials to improve these defects of keratin, such as poly(vinyl alcohol) (PVA), polylactic acid, chitosan, gelatin, poly(ethylene oxide) (PEO) and polyurethane [ 8 , 11 , 15 , 16 , 17 , 18 , 19 ]. Electrospun nanofibers prepared by blending keratin with PEO and PVA can further promote tissue regeneration, because they simulate the structure of a natural extracellular matrix (ECM) [ 17 , 19 ].…”
Section: Introductionmentioning
confidence: 99%
“…This technology was tested on ischemic chronic wounds and demonstrated enhanced healing by pro-angiogenesis, immunomodulation, and enhanced collagen synthesis. Finally, PU/gelatin/keratin electrospun hydrogels were produced in 2020 by Wan et al [ 93 ]. In this development, further enhancement was achieved by N-nitrosation of keratin to form a coupled nitrosothiol NO-donor.…”
Section: Pharmaceutical Applicationsmentioning
confidence: 99%
“…In the case of a novel carrier, its physicochemical characterization is performed first. For instance, electrospun functionalized dressings have been characterized by techniques including attenuated total reflection-Fourier transform infrared spectroscopy for the verification of functional coupling of the NO-donor to the polymer carrier; this is verified with scanning electron microscopy by visualizing the morphology of the fibers [ 35 , 93 ]. In the case of hydrogel matrices, further physicochemical characterization has been often carried-out to obtain parameters that describe the swelling capacity, degradation rate, rheological properties, and compression strength [ 94 ].…”
Section: Pharmaceutical Applicationsmentioning
confidence: 99%