Accelular nanofibrous bilayer scaffold intrapenetrated with polydopamine network and implemented into a full-thickness wound of a white-pig model affects inflammation and healing process
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F23%3AN0000019" target="_blank" >RIV/00027162:_____/23:N0000019 - isvavai.cz</a>
Alternative codes found
RIV/68378041:_____/23:00581651 RIV/00159816:_____/23:00078250 RIV/00216224:14110/23:00130597 RIV/65269705:_____/23:00078250
Result on the web
<a href="https://jnanobiotechnology.biomedcentral.com/articles/10.1186/s12951-023-01822-5" target="_blank" >https://jnanobiotechnology.biomedcentral.com/articles/10.1186/s12951-023-01822-5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/s12951-023-01822-5" target="_blank" >10.1186/s12951-023-01822-5</a>
Alternative languages
Result language
angličtina
Original language name
Accelular nanofibrous bilayer scaffold intrapenetrated with polydopamine network and implemented into a full-thickness wound of a white-pig model affects inflammation and healing process
Original language description
We fabricated a fully resorbable polydopamine (PDA) bilayered nanostructured scaffold for the treatment of defects with full loss of skin thickness. A bottom porous layer, substituting missing dermis, composed of either collagen and chitosan (Coll/Chit) or collagen and oxidized cellulose calcium salt (Coll/CaOC). A top nanofibrous layer emulating a basement membrane (BM), composed of gelatin, polycaprolactone (PCL), and CaOC. The bottom porous layer was made by a freeze-dry process, and the electrospinning process created a nanofibril mesh on the bottom porous layer. Morphological and mechanical analysis was performed using scanning electron microscopy (SEM) and RSA G2 dynamic mechanical instrument. Cytotoxicity tests, metabolic activity, proliferation, and viability of cells were performed using murine fibroblast cell lines 3T3-A31. And in vivo experiments were conducted in a porcine model, with tissue harvesting during a time period of 6 months.Polysaccharides and PDA have improved the elasticity and firmness of microfibrils, which influenced the swelling capacity and porosity of the bilayers, considering it as desirable and beneficial for restoring the function of the skin. The Coll / CaOC bilayer has shown the highest proportion of viable cells, maintained only in the presence of PDA, throughout the 14-day culture period. The expression of various cytokines in wounds has shown a non-cytotoxic effect at any stage of wound healing. It seemed that PDA supported the early stage of inflammation with expressed pro-inflammatory cytokines. At the end of healing, the expression of pro-inflammatory cytokines was comparable to that of the control samples, which means that PDA did not cause any cytotoxic or defusing effect when implanted in the skin for a longer period of time. PDA could not support the expression of pro-healing cytokines, only the expression of the examined growth factor TGF-β was higher compared to controls. This article shows that PDA at a concentration of 2mg/ml can be safely used in skin tissue applications and prepared skin grafts are ideal to meet the requirements in a proper balance between elasticity and stiffness, together with a porous architecture that allows cells to infiltrate, adhere and proliferate without cytotoxicity assessment.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
40301 - Veterinary science
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Nanobiotechnology
ISSN
1477-3155
e-ISSN
1477-3155
Volume of the periodical
21
Issue of the periodical within the volume
1
Country of publishing house
GB - UNITED KINGDOM
Number of pages
24
Pages from-to
"80"
UT code for WoS article
000945497200002
EID of the result in the Scopus database
2-s2.0-85149501628