Influence of Post-Treatment with 75% (v/v) Ethanol Vapor on the Properties of SF/P(LLA-CL) Nanofibrous Scaffolds

In order to improve the water-resistant ability of silk fibroin (SF) and SF/P(LLA-CL) blended nanofibrous scaffolds for tissue engineering applications, 75% (v/v) ethanol vapor was used to post-treat electrospun nanofibers. SEM indicated that the treated SF and SF/P(LLA-CL) nanofibrous scaffolds maintained a nanofibrous structure and possessed good water-resistant ability. Characterization of (13)C CP-MAS NMR clarified that 75% (v/v) ethanol vapor could induce SF conformation from random coil or α-helix to β-sheet. Although the water contact showed that treated SF/P(LLA-CL) blended nanofibrous scaffolds were hydrophobic, the water uptake demonstrated that their hydrophilicity was greatly superior to those of pure P(LLA-CL) nanofibrous scaffolds. Furthermore, the treated SF/P(LLA-CL) nanofibrous scaffolds, both in dry state and wet state, could retain good mechanical properties. Therefore, 75% (v/v) ethanol vapor treatment might be an ideal method to treat SF and SF/P(LLA-CL) nanofibrous scaffolds for biomedical applications.     

静电纺丝SF/PLGA纤维支架用于血管组织工程的研究

将丝素蛋白（SF）和乳酸-羟基乙酸共聚物（PLGA）溶解在六氟异丙醇中配制成溶液,采用静电纺丝技术制备了SF/PLGA纳米纤维支架,使用扫描电子显微镜（SEM）对纤维支架进行表征,研究了聚合物溶液浓度、纺丝电压、接收距离以及体积流率对纳米纤维形态的影响,从而得到纺丝的最适宜工艺参数。考察了纤维支架表面对HUVECs细胞的相容性。结果表明：HUVECs可以在SF/PLGA纤维支架表面很好的黏附和增殖,支架具有良好的细胞相容性,在组织工程领域有良好的应用前景。     

Mechanical modeling of silk fibroin/TiO2 and silk fibroin/fluoridated TiO2 nanocomposite scaffolds for bone tissue engineering

Biocompatible and biodegradable three-dimensional scaffolds are commonly porous which serve to provide suitable microenvironments for mechanical supporting and optimal cell growth. Silk fibroin (SF) is a natural and biomedical polymer with appropriate and improvable mechanical properties. Making a composite with a bioceramicas reinforcement is a general strategy to prepare a scaffold for hard tissue engineering applications. In the present study, SF was separately combined with titanium dioxide (TiO₂) and fluoridated titanium dioxide nanoparticles (TiO₂-F) as bioceramic reinforcements for bone tissue engineering purposes. At the first step, SF was extracted from Bombyx mori cocoons. Then, TiO₂ nanoparticles were fluoridated by hydrofluoric acid. Afterward, SF/TiO₂ and SF/TiO₂-F nanocomposite scaffolds were prepared by freeze-drying method to obtain a porous microstructure. Both SF/TiO₂ and SF/TiO₂-F scaffolds contained 0, 5, 10, 15 and 20 wt% nanoparticles. To evaluate the efficacy of nanoparticles addition on the mechanical properties of the prepared scaffolds, their compressive properties were assayed. Likewise, the pores morphology and microstructure of the scaffolds were investigated using scanning electron microscopy. In addition, the porosity and density of the scaffolds were measured according to the Archimedes’ principle. Afterward, compressive modulus and microstructure of the prepared scaffolds were evaluated and modeled by Gibson–Ashby’s mechanical models. The results revealed that the compressive modulus predicted by the mechanical model exactly corresponds to the experimental one. The modeling approved the honeycomb structure of the prepared scaffolds which possess interconnected pores.

     

Fabrication and intermolecular interactions of silk fibroin/hydroxybutyl chitosan blended nanofibers

The native extracellular matrix (ECM) is composed of a cross-linked porous network of multifibril collagens and glycosaminoglycans. Nanofibrous scaffolds of silk fibroin (SF) and hydroxybutyl chitosan (HBC) blends were fabricated using 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and trifluoroacetic acid (TFA) as solvents to biomimic the native ECM via electrospinning. Scanning electronic microscope (SEM) showed that relatively uniform nanofibers could be obtained when 12% SF was blended with 6% HBC at the weight ratio of 50:50. Meanwhile, the average nanofibrous diameter increased when the content of HBC in SF/HBC blends was raised from 20% to 100%. Fourier transform infrared spectra (FTIR) and (13)C nuclear magnetic resonance (NMR) showed SF and HBC molecules existed in hydrogen bonding interactions but HBC did not induce conformation of SF transforming from random coil form to β-sheet structure. X-ray diffraction (XRD) confirmed the different structure of SF/HBC blended nanofibers from both SF and HBC. Thermogravimetry-Differential thermogravimetry (TG-DTG) results demonstrated that the thermal stability of SF/HBC blend nanofibrous scaffolds was improved. The results indicated that the rearrangement of HBC and SF molecular chain formed a new structure due to stronger hydrogen bonding between SF and HBC. These electrospun SF/HBC blended nanofibers may provide an ideal tissue engineering scaffold and wound dressing.     

Green electrospun nanocuprous oxide–poly(ethylene oxide)–silk fibroin composite nanofibrous scaffolds for antibacterial dressings

Cuprous oxide (Cu₂O) nanoparticles have attracted extensive attention because of their excellent optical, catalytic, antibacterial, and antifungal properties and low cost. Nano-Cu₂O–poly(ethylene oxide) (PEO)–silk fibroin (SF) composite nanofibrous scaffolds (CNSs) were fabricated through green electrospinning to impart excellent antibacterial properties onto nanofibrous scaffolds. Scanning electron microscopy revealed that the nanofibers became more nonuniform and appeared more and more as beads in the nanofibers with increasing nano-Cu₂O concentration, and no obvious morphological changes were observed after 75% EtOH vapor treatment. Transmission electron microscopy and X-ray photoelectron spectroscopy demonstrated that nano-cuprous oxide (nano-Cu₂O) was successfully loaded into the PEO–SF nanofibers. Fourier transform infrared–attenuated total reflectance spectroscopy results indicate that nano-Cu₂O did not induce SF conformation from random coils to β sheets. The SF conformation converted from random coils to β sheets after 75% EtOH vapor treatment. The results of water contact angle testing and swelling property measurement clarified that nano-Cu₂O–PEO–SF CNSs possessed outstanding hydrophilicity. Nano-Cu₂O–PEO–SF CNSs exhibited better antibacterial activity against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus bacteria than PEO–SF nanofibrous scaffolds, and the antibacterial activity increased with increasing nano-Cu₂O concentration. Cell viability studies with pig iliac endothelial cells demonstrated that nano-Cu₂O–PEO–SF CNSs had no cytotoxicity. Nano-Cu₂O–PEO–SF CNSs are expected to be ideal biomimetic antibacterial dressings for wound healing. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47730.     

Silk fibroin‐chondroitin sulfate‐alginate porous scaffolds: Structural properties and in vitro studies

The development of porous biodegradable scaffolds is of great interest in tissue engineering. In this regard, exploration of novel biocompatible materials is needed. Silk fibroin‐chondroitin sulfate‐sodium alginate (SF‐CHS‐SA) porous hybrid scaffolds were successfully prepared via lyophilization method and crosslinked by 1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide‐ethanol treatment. According to the scanning electron microscopy studies, mean pore diameters of the scaffolds were in the range of 60–187 μm. The porosity percentage of the scaffold with SF‐CHS‐SA ratio of 70 : 15 : 15 (w/w/w %) was 92.4 ± 3%. Attenuated total reflectance Fourier transform infrared spectroscopy, X‐ray diffraction, and differential scanning calorimetry results confirmed the transition from amorphous random coil to crystalline β‐sheet in treated SF‐CHS‐SA scaffold. Compressive modulus was significantly improved in hybrid scaffold with SF‐CHS‐SA ratio of 70 : 15 : 15 (3.35 ± 0.15 MPa). Cytotoxicity assay showed that the scaffolds have no toxic effects on chondrocytes. Attachment of chondrocytes was much more improved within the SF‐CHS‐SA hybrid scaffold. Real‐time polymerase chain reaction analyses showed a significant increase in gene expression of collagen type II, aggrecan, and SOX9 and decrease in gene expression of collagen type I for SF‐CHS‐SA compared with SF scaffold. This novel hybrid scaffold can be a good candidate to be utilized as an efficient scaffold for cartilage tissue engineering. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41048.     

Fabrication and characterization of chitosan/PVA with hydroxyapatite biocomposite nanoscaffolds

Nanofibrous biocomposite scaffolds of chitosan (CS), PVA, and hydroxyapatite (HA) were prepared by electrospinning. The scaffolds were characterized by FTIR, SEM, TEM, and XRD techniques. Tensile testing was used for the characterization of mechanical properties. Mouse fibroblasts (L929) attachment and proliferation on the nanofibrous scaffold were investigated by MTT assay and SEM observation. FTIR, TEM, and XRD results showed the presence of nanoHA in the scaffolds. The scaffolds have porous nanofibrous morphology with random fibers in the range of 100–700 nm diameters. The CS/PVA (90/10) fibrous matrix (without HA) showed a tensile strength of 3.1 ± 0.2 MPa and a tensile modulus 10 ± 1 MPa with a strain at failure of 21.1 ± 0.6%. Increase the content of HA up to 2% increased the ultimate tensile strength and tensile modulus, but further increase HA up to 5–10% caused the decrease of tensile strength and tensile modulus. The attachment and growth of mouse fibroblast was on the surface of nanofibrous structure, and cells' morphology characteristics and viability were unaffected. A combination of nanofibrous CS/PVA and HA that mimics the nanoscale features of the extra cellular matrix could be promising for application as scaffolds for tissue regeneration, especially in low or nonload bearing areas. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Degradable and bioactive scaffold of calcium phosphate and calcium sulphate from self-setting cement for bone regeneration

Calcium sulphate/phosphate cement (CSPC) porous scaffolds were fabricated by introduction of calcium sulphate (CS) into calcium phosphate cement utilizing particle-leaching method. The morphology, porosity and mechanical strength as well as degradation of the CSPC scaffolds were characterized. The results reveal that the CSPC with 40 wt% CS content (40 CSPC) scaffolds with a porosity of 81% showed open macropores with the pore size of 200–500 μm. In addition, the 40 CSPC scaffolds with good degree of interconnected macropores degraded 60 wt% in Tris–HCl solution after 12 weeks. The proliferation, differentiation and morphology of MG₆₃ cells on the 40 CSPC scaffolds were determined using MTT assay, ALP activity and SEM. The results suggest that the CSPC scaffolds could stimulate cell proliferation and differentiation, indicating that CSPC scaffolds were biocompatible and had no negative effects on the cells in vitro. The CSPC scaffolds were implanted in femur bone defect of rabbits, and the in vivo biocompatibility and osteogenicity of the scaffolds were investigated. The results indicate that CSPC scaffolds exhibited good biocompatibility, degradability and osteogenesis in vivo.     

Preparation and characterization of polyhydroxybutyrate‐co‐hydroxyvalerate/silk fibroin nanofibrous scaffolds for skin tissue engineering

Nanofibrous scaffolds were obtained by co‐electrospinning poly (3‐hydroxybuty‐rate‐co‐3‐hydroxyvalerate) (PHBV) and fibroin regenerated from silk in different proportions using 1,1,1,3,3,3‐hexafluoro‐2‐isopropanol (HFIP) as solvent. Field emission scanning electron microscope (FESEM) investigation showed that the fiber diameters of the nanofibrous scaffolds ranged from 190 to 460 nm. X‐ray diffraction (XRD) and Fourier transform infrared spectroscopy analysis (FT‐IR) showed that the main structure of silk fibroin (SF) in the nanofibrous scaffold was β‐sheet. Compared to the PHBV nanofibrous scaffold, the surface hydrophilicity and water‐uptake capability of the PHBV/SF nanofibrous scaffold with 50/50 were improved. The results of cell adhesion experiment showed that the fibroblasts adhered more to the PHBV/SF nanofibrous scaffold with 50/50 than the pure PHBV nanofibrous scaffold. The proliferation of fibroblast on the PHBV/SF nanofibrous scaffold with 50/50 was higher than that on the pure PHBV nanofibrous scaffold. Our results indicated that the PHBV/SF nanofibrous scaffold with 50/50 may be a better candidate for biomedical applications such as skin tissue engineering and wound dressing. POLYM. ENG. SCI., 55:907–916, 2015. © 2014 Society of Plastics Engineers     

Sustained release of dexamethasone from drug‐loading PLGA scaffolds with specific pore structure fabricated by supercritical CO2 foaming

Inducing differentiation of bone marrow stem cells to generate new bone tissue is highly desirable by controlling the release of some osteoinductive or osteoconductive factors from porous scaffolds. In this study, dexamethasone was selected as a representative of small molecule drugs and dexamethasone‐loading porous poly(lactide‐co‐glycolide) (PLGA) scaffolds were successfully fabricated by supercritical CO₂ foaming. Scanning electron microscopy images showed that scaffolds had rough and relatively interconnected pores facilitating cells adhesion and growth. Specially, dexamethasone which was incorporated into PLGA matrix in a molecularly dispersed state could serve as a nucleation agent to be helpful for the formation of interconnected pores. Dexamethasone‐loading porous PLGA scaffolds exhibited sustained release profile, and the delivery of dexamethasone from porous scaffolds could last for up to 2 months. The cumulative released amount of dexamethasone was relevant with drug loading capacity (1.66%–2.95%) and pore structure of scaffolds; while the release behavior was anomalous (non‐Fickian) transport by fitting with the simple exponential equation, which had a diffusional exponent n higher than 0.5. It is feasible to fabricate drug‐loading porous scaffolds by supercritical CO₂ foaming with specific pore structure and sustained release profile, which can be well applied in bone tissue engineering. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46207.     

PLGA/SF blend scaffolds modified with plasmid complexes for enhancing proliferation of endothelial cells

Biomimetic scaffolds have been investigated for vascular tissue engineering for many years. However, the design of an ideal biodegradable vascular scaffold is still in progress. The optimization of poly(lactide-co-glycolide)/silk fibroin (PLGA/SF) blend composition was performed to provide the designed scaffolds with adequate mechanical properties and favorable biocompatibility for the intended application. By systematically varying the weight ratio of PLGA and SF, we could control fiber diameter and hydrophilicity as well as mechanical properties of the fibrous scaffolds. These scaffolds with a weight ratio of PLGA/SF at 70/30 exhibited excellent performance, such as tensile strength of 1.5 ± 0.1 MPa, and elongation at break of 77.4 ± 6.4%. Therefore, PLGA/SF scaffold with a weight ratio of 70/30 was chose as the matrix because it matches at best the mechanical demands for application in vascular tissue engineering. In order to promote the endothelialization of electrospun scaffolds, we used pEGFP-ZNF580 plasmid (pZNF580) complexes to modify the electrospun scaffolds by electrospraying technique. pZNF580 complexes were prepared from pZNF580 and microparticles (MPs) of amphiphilic copolymer methoxy-poly(ethylene glycol)-block-poly(3(S)-methyl-2,5-morpholinedione-co-glycolide)-graft-polyethyleneimine. Negatively charged PLGA/SF fibers adsorbed the positively charged MPs via physical deposition and electrostatic force. Scanning electron microscope image indicated the forming of composite scaffold and MPs did not change fiber’s shape and 3-D structure. Cell culture experiments demonstrated that the scaffolds modified with MPs/pZNF580 complexes could promote human umbilical vein endothelial cell growth and inhibit human umbilical artery smooth muscle cell proliferation. Our results indicated that the composite scaffolds with MPs/pZNF580 complexes could be used as a potential scaffold for vascular tissue engineering.     

Fabrication of three-dimensional interconnected porous blocks composed of robust carbonate apatite frameworks

In scaffolds used for bone regeneration, osteogenic ability increases and mechanical strength decreases with increasing porosity. To ensure both mechanical strength and osteogenesis, an optimal pore architecture is necessary. Porous glass has high porosity and high mechanical strength, as it is framed with a rigid interconnected silica network and void interspaces in the silica network. In this context, based on the porous structure of glass, we fabricated porous blocks composed of carbonate apatite (CO₃Ap), which is the major component of human bone mineral, with both high mechanical strength and high porosity. To fabricate the CO₃Ap blocks, first, calcite-polymethyl methacrylate (PMMA) mixture granules were prepared. Next, the calcite-PMMA granules were allowed to join together in the mold by fusing PMMA, resulting in the formation of porous blocks composed of interconnected calcite-PMMA granules. Next, PMMA was thermally removed and the resultant interconnected calcite granules were partially sintered. Finally, the composition of the interconnected granules was converted from calcite to CO₃Ap in a dissolution-precipitation reaction. Consequently, CO₃Ap blocks with a continuous pore architecture were successfully fabricated. The porosity and diametral tensile strength were controllable within the range of 60‒70% and 1.0‒1.5 MPa, respectively, by filling the space between the calcite-PMMA granules. As these values are suitable for clinical use, the porous CO₃Ap blocks have potential applications as scaffolds for bone regeneration.     

Nanohydroxyapatite-coated hydroxyethyl cellulose/poly (vinyl) alcohol electrospun scaffolds and their cellular response

The present study focused on the preparation of nanohydroxyapatite (nHA)-coated hydroxyethyl cellulose/polyvinyl alcohol (HEC/PVA) nanofibrous scaffolds for bone tissue engineering application. The electrospun HEC/PVA scaffolds were mineralized via alternate soaking process. FESEM revealed that the nHA was formed uniformly over the nanofibers. The nHA mineralization enhanced the tensile strength and reduced the elongation at breakage of scaffolds. The wettability of the nanofibrous scaffolds was significantly improved. The in vitro biocompatibility of scaffolds was evaluated with human osteosarcoma cells. nHA-coated scaffolds had a favorable effect on the proliferation and differentiation of osteosarcoma cell and could be a potential candidate for bone regeneration.     

Study on the properties of the electrospun silk fibroin/gelatin blend nanofibers for scaffolds

Silk fibroin (SF)/gelatin blend nanofibers membranes as scaffolds were fabricated successfully via electrospinning with different composition ratios in formic acid. The formation of intermolecular hydrogen bonds and the conformational transition of SF provided scaffolds with excellent mechanical properties. FTIR and DTA analysis showed the SF/gelatin nanofibers had more β‐sheet structures than the pure SF nanofibers. The former's breaking tenacity increased from 0.95 up to 1.60 MPa, strain at break was 7.6%, average fiber diameter was 89.2 nm, porosity was 87%, and pore diameter was 142 nm. MTT, H&E stain, and SEM results showed that the adhesion, spreading, and proliferation of human umbilic vein endothelium cells (HUVECs) and mouse fibroblasts on the SF/gelatin nanofibers scaffolds were definitely better than that on the SF nanofibers scaffolds. The scaffolds could replace the natural ECM proteins, support long‐term cell growth, form three‐dimensional networks of the nanofibrous structure, and grow in the direction of fiber orientation. Our results prove that the addition of gelatin improved the mechanical and biological properties of the pure SF nanofibers, these SF/gelatin blend nanofiber membranes are desirable for the scaffolds and may be a good candidate for blood vessel engineering scaffolds. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Mechanical strength and biocompatibility of bredigite (Ca7MgSi4O16) tissue-engineering scaffolds modified by aliphatic polyester coatings

Bredigite (Ca₇MgSi₄O₁₆) is a bioceramic with excellent bioactivity and bioresorbability; nonetheless, its inadequate mechanical strength and biocompatibility limit its tissue-engineering application. In this research, interconnected porous bredigite scaffolds were fabricated by sol-gel, sacrificial sponge replica and sintering processes for bone tissue engineering. In order to improve their strength and cytocompatibility, the scaffolds were coated with poly(lactic-co-glycolic acid) (PLGA) via immersion in acetone-based solutions containing different concentrations (5, 10 and 15% w/v) of the polymer. Based on the results, the PLGA coatings to 10% do not suppress the porosity characteristics of the scaffolds appropriate for tissue engineering. It was also found that the polymeric coatings significantly enhance the compressive strength of the ceramic scaffolds, where this alteration is improved by increasing the PLGA concentration of the coating solution. In addition, the viability of stem cells on the bredigite scaffolds are improved by using the PLGA coatings, with the optimal concentration of 10% PLGA according to MTT and cell attachment studies.     

Silk nanofibrous scaffolds assembled by natural polysaccharide konjac glucomannan

Natural silk fibroin nanofibers (SNF) have recently attracted great attention in the field of biomaterials due to their excellent biocompatibility, outstanding mechanical properties, and biomimetic nanostructures. However, the poor structural stability of SNF assembly in aqueous conditions remains a major obstacle to their biomedical application. In this work, SNF scaffolds with extracellular matrix-mimicking architecture and tunable properties were developed by using a small amount of konjac glucomannan (KGM) as a physical adhesive. Fourier transform infrared spectroscopy (FTIR) results revealed that KGM facilitated the formation of hydrogen bond networks between SNF as well as nanofibers/polysaccharide molecules, thereby reinforcing the interconnectivity between SNF. The water stability test showed that SNF scaffolds exhibited good structural stability in water when the mass ratio of KGM/SNF reached 2.5/100. Raising KGM content significantly enhanced the compression strength, modulus, and swelling ratio of the porous scaffold. Whereas, the nanofibrous morphology and porosity of the scaffolds were significantly sacrificed as KGM content exceeded 10% as evidenced by scanning electron microscopy (SEM) results. In vitro, cytocompatibility results also demonstrated the excellent biocompatibility of the biomimetic nanofibrous scaffolds, and the high porosity significantly enhanced cell viability. These results suggest that KGM-reinforced SNF scaffolds may serve as promising candidates for biomaterial applications.     

Improvement of mechanical properties of macroporous β-tricalcium phosphate bioceramic scaffolds with uniform and interconnected pore structures

The biocompatible and degradable macroporous bioceramic scaffolds with high mechanical properties and interconnected porous structures play an important role in hard tissue regeneration and bone tissue engineering applications. In this study, the improvement of mechanical properties of macroporous β-tricalcium phosphate [β-Ca₃(PO₄)₂, β-TCP] bioceramic scaffolds with uniform macropore size and interconnected pores were fabricated by impregnation of the synthesized β-TCP nano-powder slurry into polymeric frames. The microstructures, mechanical properties and in vitro degradation of the fabricated samples were investigated. For a comparison, β-TCP scaffolds were also fabricated from commercial micro-size powders under the same conditions. The resultant scaffolds showed porosities ∼65% with uniform macropore size ranging from 400 to 550 μm and interconnected pore size ∼100 μm. The compressive strength of the samples fabricated from nano-size powders reached 10.87 MPa, which was almost twice as high as those fabricated from commercial micro-size powders, and was comparable to the high-end value (2–10 MPa) of human cancellous bone. Furthermore, the degradation of the β-TCP bioceramics fabricated from nano-size powders was apparently lower than those fabricated from commercial micro-size powders, suggesting the possible control of the degradation of the scaffolds by regulating initial powder size. Regarding the excellent mechanical properties and porous structures, the obtained macroporous β-TCP bioceramic scaffolds can be used in hard tissue regeneration and bone tissue engineering applications.     

Copolymer‐induced silk‐based hydrogel with porous and nanofibrous structure

A novel physical blend method was developed to accelerate the self‐assembly process of silk fibroin (SF) solution into porous and nanofibrous hydrogel by temperature‐sensitive copolymer. Silk‐based hydrogel was firstly achieved through blending SF solution with copolymer aqueous solution and then removed the copolymer from blend solution by heat treatment (50°C) after 24 h hydrogelation. Copolymer molecules would interact with SF molecules resulting in reduction of copolymer micelles, which further affect the hydrogelation of SF solutions. Copolymers could be separated from blend solution by heat treatment under an acceptable temperature (50°C), especially the copolymer₂. Fourier transform infrared (FTIR) and X‐ray diffraction showed the blending of copolymer significantly accelerated the self‐assembly of SF into physically crosslinked β‐sheet crystals at room temperature which led to the sol‐gel transition. Results from DTA and X‐ray diffraction showed that the effect of copolymer on crystalline structure of SF in silk‐based hydrogel was very weak. SF molecules transformed from distributed globular nanoparticles to nanofilaments clustered during hydrogelation, resulting in the porous and nanofibrous structure of silk‐based hydrogel. Furthermore, silk‐based hydrogel was prepared in aqueous solution avoiding organic solvents and harsh processing conditions, suggesting that this silk‐based hydrogel could be a potential candidate scaffold for biomedical applications. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Porous β-Ca2SiO4 ceramic scaffolds for bone tissue engineering: In vitro and in vivo characterization

The biodegradable ceramic scaffolds with desirable pore size, porosity and mechanical properties play a crucial role in bone tissue engineering and bone transplantation. A novel porous β-dicalcium silicate (β-Ca₂SiO₄) ceramic scaffold was prepared by sintering the green body consisting of CaCO₃ and SiO₂ at 1300 °C, which generated interconnected pore network with proper pore size of about 300 μm and high compressive strength (28.13±5.37–10.36±0.83 MPa) following the porosity from 53.54±5.37% to 71.44±0.83%. Porous β-Ca₂SiO₄ ceramic scaffolds displayed a good biocompatibility, since human osteoblast-like MG-63 cells and goat bone mesenchymal stem cells (BMSCs) proliferated continuously on the scaffolds after 7 d culture. The porous β-Ca₂SiO₄ ceramic scaffolds revealed well apatite-forming ability when incubated in the simulated body fluid (SBF). According to the histological test, the degradation of porous β-Ca₂SiO₄ ceramic scaffolds and the new bone tissue generation in vivo were observed following 9 weeks implantation in nude mice. These results suggested that the porous β-Ca₂SiO₄ ceramic scaffolds could be potentially applied in bone tissue engineering.     

Synergistic effects of surface aminolysis and hydrolysis on improving fibroblast cell colonization within poly(L-lactide) scaffolds

This work presents a method for overcoming the low internal cell colonization within the tissue engineering scaffolds. 3D scaffolds were fabricated by the compression molding/salt leaching technique from mixtures of aminolyzed and hydrolyzed poly(L-lactide) single crystals (PLLAsc) with poly(D,L-lactide) (PDLLA) microparticles. Modified PLLAsc were used to guarantee the surface hydrophilicity, while PDLLA microparticles were used to reinforce the scaffolds. Mechanical properties, morphology, water uptake and fibroblast cell response of the scaffolds were investigated in comparison with scaffolds from only pristine, hydrolyzed, or aminolyzed PLLAsc. Results showed that the scaffolds exhibited proper morphology and hydrophilicity with an enhanced strength. Water uptake by scaffolds from modified PLLAsc was 1.9 times that from pristine PLLAsc. The scaffolds' compressive moduli increased 2.5 times by using of PDLLA (30 wt%). After cell seeding for a week, the number of cells founded on aminolyzed/hydrolyzed PLLAsc scaffolds were 4.28, 2.14, and 1.36 times that founded for pristine, aminolyzed and hydrolyzed PLLAsc scaffolds, respectively. SEM studies showed that fibroblasts migrated and spread throughout the aminolyzed/hydrolyzed PLLAsc scaffolds better than other scaffolds. Hence, combining both aminolyzed and hydrolyzed PLLAsc with PDLLA could result in a mechanically stable scaffold with an enhanced cell colonization.