In this paper, the main goal is to prepare silk fibroin nano-fiber, which is used for regenerated tissue applications. Silk scaffold nano-fibers made by electro-spinning technology can be used in regenerated tissue ap...In this paper, the main goal is to prepare silk fibroin nano-fiber, which is used for regenerated tissue applications. Silk scaffold nano-fibers made by electro-spinning technology can be used in regenerated tissue applications. The purpose of the research is to prepare a silk-fibroin nano-fiber solution for potential applications in tissue engineering. Using a degumming process, pure silk fibroin protein is extracted from silk cocoons. The protein solution for fibroin is purified, and the protein content is determined. The precise chemical composition, exact temperature, time, voltage, distance, ratio, and humidity all have a huge impact on degumming, solubility, and electro-spinning nano-fibers. The SEM investigates the morphology of silk fibroin nano-fibres at different magnifications. It also reveals the surface condition, fiber orientation, and fiber thickness of the silk fibroin nano-fiber. The results show that regenerated silk fibroin and nano-fiber can be used in silk fibroin scaffolds for various tissue engineering applications.展开更多
In order to architecturally and functionally mimic native Extracellular Matrix （ECM）, a novel micro/nano-fibrous scaffold of hydroxyapetite/poly（lactide-co-glycolide） （HA/PLGA） composite was successfully prepare...In order to architecturally and functionally mimic native Extracellular Matrix （ECM）, a novel micro/nano-fibrous scaffold of hydroxyapetite/poly（lactide-co-glycolide） （HA/PLGA） composite was successfully prepared by melt-spinning method. A porous three-dimensional scaffold fabricated by melt-molding particulate-leaching method was used as control. This kind of scaffold comprising both nanofiber and microfiber had an original structure including a nano-network favorable for cell adhe- sion, and a micro-fiber providing a strong skeleton for support. The microfibers and nanofibers were blended homogeneously in scaffold and the compression strength reached to 6.27 MPa, which was close to human trabecular bone. The typical mi- cro/nano-fibrous structure was more benefcial for the proliferation and differentiation of Bone Mesenehymal Stem Cells （BMSCs）. The calcium deposition and Alkaline Phosphatase （ALP） activity were evaluated by the differentiation of BMSCs, and the results indicated that the temporary ECM was very beneficial for the differentiation of BMSCs into maturing osteoblasts. For repairing rabbit radius defects in vivo, micro/nano-fibrous scaffold was used for the purpose of rapid bone remodeling in the defect area. The results showed that a distinct bony callus of bridging was observed at 12 weeks post-surgery and the expression of osteogenesis-related genes （bone-morphogenetic protein-2, Osteonectin, collagen-I） increased because of the ECM-like structure. Based on the results, the novel micro/nano-fibrous scaffold might be a promising candidate for bone tissue engi- neering.展开更多
In this study, poly（L-lactic acid）/ammonium persulfate doped-polypyrrole composite fibrous scaffolds with moderate conductivity were produced by combining electrospinning with in situ polymerization. PC12 cells were...In this study, poly（L-lactic acid）/ammonium persulfate doped-polypyrrole composite fibrous scaffolds with moderate conductivity were produced by combining electrospinning with in situ polymerization. PC12 cells were cultured on these fibrous scaffolds and their growth following electrical stimulation （0-20.0 μA stimulus intensity, for 1-4 days） was observed using inverted light microscopy, and scanning electron microscopy coupled with the MTT cell viability test. The results demonstrated that the poly（L-lactic acid）/ammonium persulfate doped-polypyrrole fibrous scaffold was a dual multi-porous micro/nano fibrous scaffold. An electrical stimulation with a current intensity 5.0- 10.0 μAfor about 2 days enhanced neuronal growth and neurite outgrowth, while a high current intensity （over 15.0 μA） suppressed them. These results indicate that electrical stimulation with a moderate current intensity for an optimum time frame can promote neuronal growth and neurite outgrowth in an intensity- and time-dependent manner.展开更多
文摘In this paper, the main goal is to prepare silk fibroin nano-fiber, which is used for regenerated tissue applications. Silk scaffold nano-fibers made by electro-spinning technology can be used in regenerated tissue applications. The purpose of the research is to prepare a silk-fibroin nano-fiber solution for potential applications in tissue engineering. Using a degumming process, pure silk fibroin protein is extracted from silk cocoons. The protein solution for fibroin is purified, and the protein content is determined. The precise chemical composition, exact temperature, time, voltage, distance, ratio, and humidity all have a huge impact on degumming, solubility, and electro-spinning nano-fibers. The SEM investigates the morphology of silk fibroin nano-fibres at different magnifications. It also reveals the surface condition, fiber orientation, and fiber thickness of the silk fibroin nano-fiber. The results show that regenerated silk fibroin and nano-fiber can be used in silk fibroin scaffolds for various tissue engineering applications.
基金This research was financially supported by Na- tional Natural Science Foundation of China （Projects 51103149, 51273195 and 51321062）.
文摘In order to architecturally and functionally mimic native Extracellular Matrix （ECM）, a novel micro/nano-fibrous scaffold of hydroxyapetite/poly（lactide-co-glycolide） （HA/PLGA） composite was successfully prepared by melt-spinning method. A porous three-dimensional scaffold fabricated by melt-molding particulate-leaching method was used as control. This kind of scaffold comprising both nanofiber and microfiber had an original structure including a nano-network favorable for cell adhe- sion, and a micro-fiber providing a strong skeleton for support. The microfibers and nanofibers were blended homogeneously in scaffold and the compression strength reached to 6.27 MPa, which was close to human trabecular bone. The typical mi- cro/nano-fibrous structure was more benefcial for the proliferation and differentiation of Bone Mesenehymal Stem Cells （BMSCs）. The calcium deposition and Alkaline Phosphatase （ALP） activity were evaluated by the differentiation of BMSCs, and the results indicated that the temporary ECM was very beneficial for the differentiation of BMSCs into maturing osteoblasts. For repairing rabbit radius defects in vivo, micro/nano-fibrous scaffold was used for the purpose of rapid bone remodeling in the defect area. The results showed that a distinct bony callus of bridging was observed at 12 weeks post-surgery and the expression of osteogenesis-related genes （bone-morphogenetic protein-2, Osteonectin, collagen-I） increased because of the ECM-like structure. Based on the results, the novel micro/nano-fibrous scaffold might be a promising candidate for bone tissue engi- neering.
基金supported by the National Natural Science Foundation of China,No.51073072the Natural Science Foundation of Zhejiang Province in China,No.Y4100745+1 种基金the Key Laboratory Open Foundation of Advanced Textile Materials&Manufacturing Technology of Zhejiang Sci-Tech University from Ministry of Education of China,No.2009007the Science and Technology Commission of Jiaxing Municipality Program,No.2010AY1089
文摘In this study, poly（L-lactic acid）/ammonium persulfate doped-polypyrrole composite fibrous scaffolds with moderate conductivity were produced by combining electrospinning with in situ polymerization. PC12 cells were cultured on these fibrous scaffolds and their growth following electrical stimulation （0-20.0 μA stimulus intensity, for 1-4 days） was observed using inverted light microscopy, and scanning electron microscopy coupled with the MTT cell viability test. The results demonstrated that the poly（L-lactic acid）/ammonium persulfate doped-polypyrrole fibrous scaffold was a dual multi-porous micro/nano fibrous scaffold. An electrical stimulation with a current intensity 5.0- 10.0 μAfor about 2 days enhanced neuronal growth and neurite outgrowth, while a high current intensity （over 15.0 μA） suppressed them. These results indicate that electrical stimulation with a moderate current intensity for an optimum time frame can promote neuronal growth and neurite outgrowth in an intensity- and time-dependent manner.
