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基于壳聚糖的膜在背褶腔大鼠模型中用于皮肤伤口修复

Chitosan-Based Membranes for Skin Wound Repair in a Dorsal Fold Chamber Rat Model.

作者信息

Casimiro Maria Helena, Ferreira Luís M, Santos Pedro M P, Leal João P, Rodrigues Gabriela, Iria Inês, Alves Sara, Pais Diogo, Casal Diogo

机构信息

Centro de Ciências e Tecnologias Nucleares (C2TN), Instituto Superior Técnico (IST), Universidade de Lisboa, 2695-066 Bobadela, Portugal.

Departamento de Engenharia e Ciências Nucleares (DECN), Instituto Superior Técnico (IST), Universidade de Lisboa, 2695-066 Bobadela, Portugal.

出版信息

Pharmaceutics. 2022 Dec 7;14(12):2736. doi: 10.3390/pharmaceutics14122736.

DOI:10.3390/pharmaceutics14122736
PMID:36559232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9784945/
Abstract

Frequently, deep partial and full-thickness skin wounds do not spontaneously regenerate. To restore the normal function of skin, epidermal and dermal components have to be supplied to the wound bed by grafting various substrates. Available options are limited and frequently costly. Herein, authors present a possible approach using 3D skin scaffolds capable of mimicking structure and biological functions of the extracellular matrix, providing, in parallel, a good environment for cell attachment, proliferation and differentiation. Low-molecular weight chitosan-based membranes were prepared by freeze-drying and ionizing radiation techniques to be used as skin scaffolds. Poly (vinyl alcohol), PVA, vinyl pyrrolidone, VP, and gelatin from cold water fish were incorporated. Information regarding membranes' physical-chemical properties from SEM analysis, swelling and weight loss, together with biological response through in vitro assays (using Human Caucasian Fetal Foreskin Fibroblast) allowed the selection of an optimized batch of membranes that was used as skin scaffold in a dorsal rat model wound. The in vivo implantation assays (in Wistar rats) resulted in very promising results: (i) healing process faster than control; (ii) good vascularization; (iii) viable new tissues morphologically functional.

摘要

深度部分厚度和全层皮肤伤口通常不会自发再生。为恢复皮肤的正常功能,必须通过移植各种基质向伤口床提供表皮和真皮成分。现有的选择有限且往往成本高昂。在此,作者提出了一种可能的方法,即使用能够模拟细胞外基质结构和生物学功能的3D皮肤支架,同时为细胞附着、增殖和分化提供良好环境。通过冷冻干燥和电离辐射技术制备了基于低分子量壳聚糖的膜,用作皮肤支架。加入了聚乙烯醇(PVA)、乙烯基吡咯烷酮(VP)和冷水鱼明胶。通过扫描电子显微镜分析、膨胀和失重获得的有关膜的物理化学性质的信息,以及通过体外试验(使用人类高加索胎儿包皮成纤维细胞)得出的生物学反应,使得能够选择一批优化的膜,将其用作大鼠背部模型伤口的皮肤支架。体内植入试验(在Wistar大鼠中)产生了非常有前景的结果:(i)愈合过程比对照组快;(ii)良好的血管化;(iii)形态功能正常的存活新组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/f28600d1c0cf/pharmaceutics-14-02736-g012.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/7f11df35f9bc/pharmaceutics-14-02736-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/890a11d524b9/pharmaceutics-14-02736-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/9c64e5648056/pharmaceutics-14-02736-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/5af447864b1b/pharmaceutics-14-02736-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/fb75ca58e808/pharmaceutics-14-02736-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/04262acf8cde/pharmaceutics-14-02736-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/62d67884aaca/pharmaceutics-14-02736-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/523bd72697cd/pharmaceutics-14-02736-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/f28600d1c0cf/pharmaceutics-14-02736-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/bb294a8f1bd9/pharmaceutics-14-02736-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/b518ae09f262/pharmaceutics-14-02736-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/9eaaef83d58b/pharmaceutics-14-02736-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/7f11df35f9bc/pharmaceutics-14-02736-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/890a11d524b9/pharmaceutics-14-02736-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/9c64e5648056/pharmaceutics-14-02736-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/5af447864b1b/pharmaceutics-14-02736-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/fb75ca58e808/pharmaceutics-14-02736-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/04262acf8cde/pharmaceutics-14-02736-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/62d67884aaca/pharmaceutics-14-02736-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/523bd72697cd/pharmaceutics-14-02736-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/9784945/f28600d1c0cf/pharmaceutics-14-02736-g012.jpg

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