Evaluation of sericin/collagen membranes as prospective wound dressing biomaterial

被引:161
作者
Akturk, Omer [1 ]
Tezcaner, Aysen [1 ,2 ]
Bilgili, Hasan [3 ]
Deveci, M. Salih [4 ]
Gecit, M. Rusen [1 ]
Keskin, Dilek [1 ,2 ]
机构
[1] Middle E Tech Univ, Dept Engn Sci, TR-06531 Ankara, Turkey
[2] Middle E Tech Univ, Grad Dept Biotechnol, TR-06531 Ankara, Turkey
[3] Middle E Tech Univ, Fac Vet Med, Dept Surg, TR-06110 Ankara, Turkey
[4] Gulhane Mil Med Acad, Fac Med, Dept Pathol, Ankara, Turkey
关键词
Sericin; Collagen; Wound dressing; Membrane; Biocompatibility; IN-VITRO; SKIN SUBSTITUTES; SILK SERICIN; CELL-ADHESION; PROTEIN; MATRIX; ATTACHMENT; SCAFFOLDS; GROWTH; FILM;
D O I
10.1016/j.jbiosc.2011.05.014
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Sericin, a silk protein, has high potential for use in biomedical applications. In this study, wound dressing membranes of Sericin (S) and Collagen (C) were prepared by glutaraldehyde cross-linking at S/C; 2:1,1:1, 1:2, and 0:1 weight ratios. They were stable in water for 4 weeks. However, increasing the proportion of sericin had decreasing effect on the membrane stability. Water swelling property of membranes was enhanced with sericin. The highest water swelling was obtained in 1:1 group (9.06 g/g), but increasing collagen or sericin content in the membranes had a diminishing effect. Highest water vapor transmission rate was obtained with 1:2 group (1013.80 g/m(2)/day). Oxygen permeability results showed that 1:2 (7.67 mg/L) and 2:1 (7.85 mg/L) SIC groups were better than the other groups. While sericin decreased the tensile strength and elongation of membranes, it increased modulus. Sericin also increased brittleness of membranes, but their UTS range (24.93-44.92 MPa) was still suitable for a wound dressing. Membranes were not penetrable to microorganisms. Cytotoxicity studies showed that fibroblasts and keratinocytes attached and gained their characteristic morphologies. They also proliferated on membranes significantly. After 1 week of subcutaneous implantation, a fibrous capsule formed around all membranes with an acute inflammation. Sericin containing membranes showed signs of degradation (at 2nd week), while collagen only membranes remained largely intact. Eventually, sericin containing membranes degraded in 3 weeks with moderate inflammatory response. Overall results suggest that sericin/collagen membranes would be favorable as wound dressing material when sericin ratio is less than or equal to the collagen component. (C) 2011, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:279 / 288
页数:10
相关论文
共 48 条
[1]
Foreign body reaction to biomaterials [J].
Anderson, James M. ;
Rodriguez, Analiz ;
Chang, David T. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :86-100
[2]
The effects of sericin cream on wound healing in rats [J].
Aramwit, Pornanong ;
Sangcakul, Areeporn .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2007, 71 (10) :2473-2477
[3]
Monitoring of inflammatory mediators induced by silk sericin [J].
Aramwit, Pornanong ;
Kanokpanont, Sorada ;
De-Eknamkul, Wanchai ;
Srichana, Teerapol .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2009, 107 (05) :556-561
[4]
Skin substitutes: a review [J].
Balasubramani, M ;
Kumar, TR ;
Babu, M .
BURNS, 2001, 27 (05) :534-544
[5]
Electrospun collagen/chitosan nanofibrous membrane as wound dressing [J].
Chen, Jyh-Ping ;
Chang, Gwo-Yun ;
Chen, Jan-Kan .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 313 :183-188
[6]
Tissue response to partially in vitro predegraded poly-L-lactide implants [J].
De Jong, WH ;
Bergsma, JE ;
Robinson, JE ;
Bos, RRM .
BIOMATERIALS, 2005, 26 (14) :1781-1791
[7]
HAARER JC, 2006, INTRO BIOMATERIALS B, P122
[8]
INTERSTITIAL CYSTITIS AND SILK ALLERGY [J].
HOLLANDER, DH .
MEDICAL HYPOTHESES, 1994, 43 (03) :155-156
[9]
INTEGRINS - VERSATILITY, MODULATION, AND SIGNALING IN CELL-ADHESION [J].
HYNES, RO .
CELL, 1992, 69 (01) :11-25
[10]
THEORETICAL-ANALYSIS OF IN-VIVO MACROPHAGE ADHESION AND FOREIGN-BODY GIANT-CELL FORMATION ON POLYDIMETHYLSILOXANE, LOW-DENSITY POLYETHYLENE, AND POLYETHERURETHANES [J].
KAO, WYJ ;
ZHAO, QH ;
HILTNER, A ;
ANDERSON, JM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1994, 28 (01) :73-79