PMID- 32708645 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200928 IS - 2073-4360 (Electronic) IS - 2073-4360 (Linking) VI - 12 IP - 7 DP - 2020 Jul 16 TI - Effects of Electrospun Fibrous Membranes of PolyCaprolactone and Chitosan/Poly(Ethylene Oxide) on Mouse Acute Skin Lesions. LID - 10.3390/polym12071580 [doi] LID - 1580 AB - Polycaprolactone (PCL) is a synthetic polymer with good mechanical properties that are useful to produce biomaterials of clinical application. It can be successfully combined with chitosan, which enhances the biomaterial properties through the modulation of molecular and cellular mechanisms. The objective of this study was to evaluate the effects of the use of electrospun fibrous membranes consisting of polycaprolactone (PCL) or polycaprolactone coated with chitosan and poly(ethylene oxide) (PCL+CHI/PEO) on mouse skin lesions. Sixty four Black-57 mice were divided into PCL and PCL+CHI/PEO groups. A 1 cm(2) lesion was made on the animals' backs, and the membranes were sutured in place. The tissues were extracted on the 3rd, 7th, and 14th days after the lesion. The tissues were analyzed by histology with Hematoxylin and Eosin (H&E) and Sirius Red stains, morphometry, immunohistochemistry, and Western blot. On the 3rd, 6th, and 9th days after the lesion, the PCL+CHI/PEO group showed a higher wound-healing rate (WHR). On the 3 day, the PCL+CHI/PEO group showed a greater amount of inflammatory infiltrate, greater expression of proliferating cell nuclear antigen (PCNA), and smooth muscle actin (alpha-SMA) (p < 0.05) compared to the PCL group. On the 7th day after the lesion, the PCL+CHI/PEO group showed a greater amount of inflammatory infiltrate, expression of Tumor Necrosis Factor (TNF-alpha) and PCNA (p < 0.05). In addition, it showed a greater immunolabeling of Monocyte Chemoattractant Protein-1 (MCP-1) and deposition of collagen fibers compared to the PCL group. The PCL+CHI/PEO membrane modulated the increase in the inflammatory infiltrate, the expression of MCP-1, PCNA, and alpha-SMA in lesions of mice. FAU - Zanchetta, Flavia Cristina AU - Zanchetta FC AUID- ORCID: 0000-0002-5934-9683 AD - School of Nursing, University of Campinas, Campinas CEP 13083887, Brazil. FAU - Trinca, Rafael Bergamo AU - Trinca RB AUID- ORCID: 0000-0002-8283-090X AD - Department of Engineering of Materials and of Bioprocess, School of Chemical Engineering, University of Campinas, Campinas CEP 13083852, Brazil. FAU - Gomes Silva, Juliany Lino AU - Gomes Silva JL AUID- ORCID: 0000-0002-2930-103X AD - School of Nursing, University of Campinas, Campinas CEP 13083887, Brazil. FAU - Breder, Jessica da Silva Cunha AU - Breder JDSC AD - School of Nursing, University of Campinas, Campinas CEP 13083887, Brazil. FAU - Cantarutti, Thiago Anselmo AU - Cantarutti TA AD - School of Nursing, University of Campinas, Campinas CEP 13083887, Brazil. FAU - Consonni, Silvio Roberto AU - Consonni SR AUID- ORCID: 0000-0003-3149-021X AD - Department of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas, Campinas CEP 13083970, Brazil. FAU - Moraes, Angela Maria AU - Moraes AM AUID- ORCID: 0000-0002-5813-332X AD - Department of Engineering of Materials and of Bioprocess, School of Chemical Engineering, University of Campinas, Campinas CEP 13083852, Brazil. FAU - Pereira de Araujo, Eliana AU - Pereira de Araujo E AD - School of Nursing, University of Campinas, Campinas CEP 13083887, Brazil. FAU - Saad, Mario Jose Abdalla AU - Saad MJA AD - Department of Internal Medicine, University of Campinas, Campinas CEP 13083887, Brazil. FAU - Adams, Gary G AU - Adams GG AUID- ORCID: 0000-0002-0335-2162 AD - School of Health Sciences, Faculty of Medicine, The University of Nottingham, C Floor, South Block Link, Queen's Medical Centre, Nottingham NG7 2HA, UK. FAU - Melo Lima, Maria Helena AU - Melo Lima MH AUID- ORCID: 0000-0001-6521-8324 AD - School of Nursing, University of Campinas, Campinas CEP 13083887, Brazil. LA - eng GR - 307139/2015-8 and 307829/2018-9/Conselho Nacional de Desenvolvimento Cientifico e Tecnologico/ PT - Journal Article DEP - 20200716 PL - Switzerland TA - Polymers (Basel) JT - Polymers JID - 101545357 PMC - PMC7408160 OTO - NOTNLM OT - C57BL/6J mice OT - chitosan OT - electrospinning OT - polycaprolactone OT - wound dressing OT - wound healing COIS- The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results. EDAT- 2020/07/28 06:00 MHDA- 2020/07/28 06:01 PMCR- 2020/07/16 CRDT- 2020/07/26 06:00 PHST- 2020/06/12 00:00 [received] PHST- 2020/07/09 00:00 [revised] PHST- 2020/07/13 00:00 [accepted] PHST- 2020/07/26 06:00 [entrez] PHST- 2020/07/28 06:00 [pubmed] PHST- 2020/07/28 06:01 [medline] PHST- 2020/07/16 00:00 [pmc-release] AID - polym12071580 [pii] AID - polymers-12-01580 [pii] AID - 10.3390/polym12071580 [doi] PST - epublish SO - Polymers (Basel). 2020 Jul 16;12(7):1580. doi: 10.3390/polym12071580.