Tamada Yasushi
National Institute of Agrobiological Sciences, 1-2 Owashi, Tsukuba, Ibaraki 305-8634.
Biomacromolecules. 2005 Nov-Dec;6(6):3100-6. doi: 10.1021/bm050431f.
A new process to form fibroin spongy porous 3-D structure is reported herein. The process involves freezing and thawing fibroin aqueous solution in the presence of a small amount of an organic solvent. The process requires no freeze-drying, chemical cross-linking, or the aid of other polymeric materials. The solvent concentration, fibroin concentration, freezing temperature, and freezing duration affect the sponge formation, its porous structure, and its mechanical properties. Measurements by XRD and FTIR indicate that silk I and silk II crystalline structures exist in the fibroin sponge and that the secondary structure of fibroin is transformed to a beta-sheet from a random coil during this process. The tensile strength decreased slightly, but the fibroin sponge showed no deformation after autoclaving. Therefore, the fibroin sponge was sterilized using an autoclave. For 3 weeks, MC3T3 cells proliferated in the sterilized fibroin sponge. The fibroin sponge formed by this new process is applicable as a tissue-engineering scaffold because it is formed from biocompatible pure silk fibroin and offers both porous structure and mechanical properties that are suitable for cell growth and handling.
本文报道了一种形成丝素蛋白海绵状多孔三维结构的新方法。该方法包括在少量有机溶剂存在下对丝素蛋白水溶液进行冻融处理。该方法无需冷冻干燥、化学交联或其他聚合材料的辅助。溶剂浓度、丝素蛋白浓度、冷冻温度和冷冻持续时间会影响海绵的形成、其多孔结构及其力学性能。XRD和FTIR测量表明,丝素蛋白海绵中存在丝I和丝II晶体结构,并且在此过程中丝素蛋白的二级结构从无规卷曲转变为β-折叠。拉伸强度略有下降,但丝素蛋白海绵在高压灭菌后未出现变形。因此,使用高压灭菌器对丝素蛋白海绵进行了灭菌。MC3T3细胞在灭菌后的丝素蛋白海绵中增殖了3周。通过这种新方法形成的丝素蛋白海绵可作为组织工程支架应用,因为它由生物相容性纯丝素蛋白形成,具有适合细胞生长和处理的多孔结构和力学性能。