Detailed Information on Publication Record
2023
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
KACVINSKA, Katarina, Veronika PAVLINAKOVA, Petr POLACEK, Lenka MICHLOVSKA, Veronika HEFKA BLAHNOVA et. al.Basic information
Original 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
Authors
KACVINSKA, Katarina (203 Czech Republic), Veronika PAVLINAKOVA (203 Czech Republic), Petr POLACEK (203 Czech Republic), Lenka MICHLOVSKA (203 Czech Republic), Veronika HEFKA BLAHNOVA (203 Czech Republic), Eva FILOVA (203 Czech Republic), Martin KNOZ (203 Czech Republic, belonging to the institution), Břetislav LIPOVÝ (203 Czech Republic, belonging to the institution), Jakub HOLOUBEK (203 Czech Republic, belonging to the institution), Martin FALDYNA (203 Czech Republic), Zdeněk PAVLOVSKÝ (203 Czech Republic, belonging to the institution), Monika VICENOVA (203 Czech Republic), Michaela CVANOVÁ (203 Czech Republic, belonging to the institution), Jiří JARKOVSKÝ (203 Czech Republic, belonging to the institution) and Lucy VOJTOVA (203 Czech Republic, guarantor)
Edition
JOURNAL OF NANOBIOTECHNOLOGY, LONDON, BIOMED CENTRAL LTD, 2023, 1477-3155
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30212 Surgery
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 10.200 in 2022
RIV identification code
RIV/00216224:14110/23:00130597
Organization unit
Faculty of Medicine
UT WoS
000945497200002
Keywords in English
Bilayer; Chitosan; Collagen; Oxidized cellulose; Polydopamine; Wound healing
Tags
International impact, Reviewed
Změněno: 5/4/2024 08:20, Mgr. Tereza Miškechová
Abstract
V originále
Treatment of complete loss of skin thickness requires expensive cellular materials and limited skin grafts used as temporary coverage. This paper presents an acellular bilayer scaffold modified with polydopamine (PDA), which is designed to mimic a missing dermis and a basement membrane (BM). The alternate dermis is made from freeze-dried collagen and chitosan (Coll/Chit) or collagen and a calcium salt of oxidized cellulose (Coll/CaOC). Alternate BM is made from electrospun gelatin (Gel), polycaprolactone (PCL), and CaOC. Morphological and mechanical analyzes have shown that PDA significantly improved the elasticity and strength of collagen microfibrils, which favorably affected swelling capacity and porosity. PDA significantly supported and maintained metabolic activity, proliferation, and viability of the murine fibroblast cell lines. The in vivo experiment carried out in a domestic Large white pig model resulted in the expression of pro-inflammatory cytokines in the first 1–2 weeks, giving the idea that PDA and/or CaOC trigger the early stages of inflammation. Otherwise, in later stages, PDA caused a reduction in inflammation with the expression of the anti-inflammatory molecule IL10 and the transforming growth factor β (TGFβ1), which could support the formation of fibroblasts. Similarities in treatment with native porcine skin suggested that the bilayer can be used as an implant for full-thickness skin wounds and thus eliminate the use of skin grafts.
Links
NU22-08-00454, research and development project |
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90110, large research infrastructures |
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