New crosslinkers for electrospun chitosan fibre mats. I. Chemical analysis

被引:51
|
作者
Austero, Marjorie S. [1 ]
Donius, Amalie E. [1 ]
Wegst, Ulrike G. K. [1 ,2 ]
Schauer, Caroline L. [1 ]
机构
[1] Drexel Univ, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[2] Dartmouth Coll, Thayer Sch Engn, Hanover, NH 03755 USA
基金
美国国家科学基金会;
关键词
electrospinning; chitosan; biopolymer; genipin; diisocyanate; epichlorohydrin; IN-VITRO EVALUATION; AQUEOUS-SOLUTION; BLUE PIGMENTS; SILK FIBROIN; LINKING; GENIPIN; CHITIN; POLYMER; EPICHLOROHYDRIN; METHYLAMINE;
D O I
10.1098/rsif.2012.0241
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chitosan (CS), the deacetylated form of chitin, the second most abundant, natural polysaccharide, is attractive for applications in the biomedical field because of its biocompatibility and resorption rates, which are higher than chitin. Crosslinking improves chemical and mechanical stability of CS. Here, we report the successful utilization of a new set of crosslinkers for electrospun CS. Genipin, hexamethylene-1,6-diaminocarboxysulphonate (HDACS) and epichlorohydrin (ECH) have not been previously explored for crosslinking of electrospun CS. In this first part of a two-part publication, we report the morphology, determined by field emission scanning electron microscopy (FESEM), and chemical interactions, determined by Fourier transform infrared microscopy, respectively. FESEM revealed that CS could successfully be electrospun from trifluoroacetic acid with genipin, HDACS and ECH added to the solution. Diameters were 267 +/- 199 nm, 644 +/- 359 nm and 896 +/- 435 nm for CS-genipin, CS-HDACS and CS-ECH, respectively. Short- (15 min) and long-term (72 h) dissolution tests (T-600) were performed in acidic, neutral and basic pHs (3, 7 and 12). Post-spinning activation by heat and base to enhance crosslinking of CS-HDACS and CS-ECH decreased the fibre diameters and improved the stability. In the second part of this publication, we report the mechanical properties of the fibres.
引用
收藏
页码:2551 / 2562
页数:12
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