Effect of silk fibroin nanofibers containing silver sulfadiazine on wound healing

被引:52
作者
Jeong, Lim [1 ]
Kim, Min Hee [1 ]
Jung, Ju-Young [2 ]
Min, Byung Moo [3 ]
Park, Won Ho [1 ]
机构
[1] Chungnam Natl Univ, Dept Adv Organ Mat & Text Syst Engn, Taejon 305764, South Korea
[2] Chungnam Natl Univ, Coll Vet Med, Taejon 305764, South Korea
[3] Seoul Natl Univ, Sch Dent, Dept Oral Biochem, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
silk fibroin; silver sulfadiazine; nanofibrous matrix; wound healing; BURNS; NANOPARTICLES; FIBROBLASTS; KERATINOCYTES; ACTICOAT(TM); DRESSINGS; NITRATE;
D O I
10.2147/IJN.S71295
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: One of the promising applications of silk fibroin (SF) in biomedical engineering is its use as a scaffolding material for skin regeneration. The purpose of this study was to determine the wound healing effect of SF nanofibrous matrices containing silver sulfadiazine (SSD) wound dressings. Methods: An SF nanofibrous matrix containing SSD was prepared by electrospinning. The cell attachment and spreading of normal human epidermal keratinocytes (NHEK) and normal human epidermal fibroblasts (NHEF) to SF nanofibers containing three different concentrations of SSD contents (0.1, 0.5, and 1.0 wt%) were determined. In addition, a rat wound model was used in this study to determine the wound healing effect of SF nanofibers containing SSD compared with that of Acticoat T, a commercially available wound dressing. Results: The number of NHEK and NHEF attached to SF nanofibers containing SSD decreased when the concentration of SSD increased. The number of attached NHEF cells was lower than that of attached NHEK cells. The SF matrix with 1.0 wt% SSD produced faster wound healing than Acticoat (TM) although 1.0 wt% SSD inhibited the attachment of epidermal cells to SF nanofibers in vitro. Conclusion: The cytotoxic effects of SF nanofibers with SSD should be considered in the development of silver-release dressings for wound healing through its antimicrobial activity. It is challenging to design wound dressings that maximize antimicrobial activity and minimize cellular toxicity.
引用
收藏
页码:5277 / 5287
页数:11
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