Cu(II) ion loading in silk fibroin scaffolds with silk I structure

被引:22
作者
Hua, Jinsheng [1 ]
You, Haining [2 ]
Li, Xiufang [2 ]
You, Renchuan [2 ]
Ma, Likun [1 ]
机构
[1] Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Cardiol, Div Life Sci & Med, Hefei 230036, Peoples R China
[2] Wuhan Text Univ, Sch Text Sci & Engn, State Key Lab Hubei New Text Mat & Adv Proc Techn, Wuhan 430200, Peoples R China
基金
中国国家自然科学基金;
关键词
Silk biomaterials; Metal ion loading; Copper ions; BIOACTIVE GLASS; METALLIC-IONS; COPPER; ANGIOGENESIS; CONFORMATION; TRANSITIONS; MECHANISM; NMR; PH; CU;
D O I
10.1016/j.ijbiomac.2020.04.094
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metal ions play important roles in the diverse biochemical reactions associated with many cell signalling pathways. The modification of biomaterials with metal ions may offer a promising approach to stimulate cellular activity for improving tissue regeneration. Here, copper ion loading as a potential therapeutic agent in silk fibroin (SF) scaffolds was investigated. Freezing-annealing was used to induce silk I crystallization for forming water insoluble SF scaffolds. Cu(II) ions were entrapped into SF scaffolds with different ratios by forming silk I crystal networks when copper chloride dihydrate was less than 5.0 wt%, producing water-stable materials. Moreover, it was found that copper ion chelation further enhanced SF stability when a low amount copper chloride was loaded. Increasing copper chloride content weakened silk I crystallization and Cu(II) ion chelation, rendering SF scaffolds unstable in water. Above 5.0 wt% copper chloride dihydrate, silk I crystallization was prevented. Finally, silk I scaffold with 1.5 wt% copper chloride dihydrate showed the strongest water-stability and highest loading efficiency. The results provide valuable data for understanding the effect of metal ions in freezing induced SF crystallization, and also offer options for preparing novel Cu(II)-functionalized SF scaffolds. (c) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:275 / 281
页数:7
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