2016
DOI: 10.1039/c5ra19529b
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Fabrication and characterization of a collagen coated electrospun poly(3-hydroxybutyric acid)–gelatin nanofibrous scaffold as a soft bio-mimetic material for skin tissue engineering applications

Abstract: The collagen coated nanofibrous scaffold mimics the function of the extra cellular matrix with good biocompatibility, cell adhesion, cell proliferation and aids to provide as a promising tool in skin tissue engineering application.

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Cited by 72 publications
(26 citation statements)
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“…The effective strategy is to load the antibacterial drugs into the wound dressing and release it slowly to the wound to achieve a long-lasting local antibacterial effect. An ideal wound dressing should: 1) Be close to the wound to absorb excess exudate and maintain a moist environment in the wound; 2) be nontoxic and have no immunogenicity; and 3) maintain moisture absorption ability, block the invasion of external bacteria and pathogenic organisms, and be able to release antibacterial drugs slowly to prevent infection of the wound [34][35][36]. In this study, we fabricated porous PHMB/SF sponges with antibacterial function through electrostatic interaction and by freeze-drying.…”
Section: Discussionmentioning
confidence: 99%
“…The effective strategy is to load the antibacterial drugs into the wound dressing and release it slowly to the wound to achieve a long-lasting local antibacterial effect. An ideal wound dressing should: 1) Be close to the wound to absorb excess exudate and maintain a moist environment in the wound; 2) be nontoxic and have no immunogenicity; and 3) maintain moisture absorption ability, block the invasion of external bacteria and pathogenic organisms, and be able to release antibacterial drugs slowly to prevent infection of the wound [34][35][36]. In this study, we fabricated porous PHMB/SF sponges with antibacterial function through electrostatic interaction and by freeze-drying.…”
Section: Discussionmentioning
confidence: 99%
“…Green fluorescence is emitted by calcein that has been converted from nonfluorescent calcein through acetoxymethylester hydrolysis by intracellular esterases of viable cells to fluorescent calcein. Blue fluorescence is emitted by DAPI binding to AT regions of sdDNA, therefore marking all present cell nuclei …”
Section: Methodsmentioning
confidence: 99%
“…Cell attachment and proliferation of both NIH 3T3 fibroblast and human keratinocytes (HaCaT) cell lines were quantified for live cell assay at regular time intervals (6, 12, 24 and 48 h), the medium was removed and the cells were fixed with 4% paraformaldehyde and washed with PBS for several times. Furthermore, each cell was stained with calcein AM solution (2 μM; 400 μl) and incubated for 30 min at 37 • C. Then, the plates with scaffold were washed with PBS for several times and viewed at fluorescence microscope (EVOS FLoid Cell Imaging Station, Thermo Fisher Scientific, USA) [26,27].…”
Section: Biological Propertiesmentioning
confidence: 99%
“…About 100 ml [10 5 CFU (colony forming units)] of each bacterial culture was spread over the agar surface (Muller-Hinton agars) using a sterile glass spreader. The plates were then incubated for 24 h at 37 • C. The antibacterial activity was evaluated by measuring the zone of inhibition against the test organism [26].…”
Section: Antimicrobial Activitymentioning
confidence: 99%