Heterogeneous porous PLLA/PCL fibrous scaffold for bone tissue regeneration.

Bone tissue engineering has become one of the most promising therapeutic methods to treat bone defects. A suitable scaffolding material to regenerate new bone tissues should have a high specific surface area, high porosity and a suitable surface structure which benefit cell attachment, proliferation, and differentiation. In this study, an acetone post-treatment strategy was developed to generate heterogeneous structure. After PLLA/PCL nanofibrous membranes were electrospun and collected, they were treated with acetone to generate a highly porous structure. Meanwhile, part of PCL was extracted from the fibre and enriched on the fibre surface. The cell affinity of the nanofibrous membrane was verified by human osteoblast-like cells assay. The proliferation rate of heterogeneous samples increased 190.4 %, 265.5 % and 137.9 % at day 10 compared with pristine samples. These results demonstrated that the heterogeneous PLLA/PCL nanofibrous membranes could enhance osteoblast adhesion and proliferation. With high surface area (average surface area 36.302 m2/g) and good mechanical properties (average Young's modulus 1.65 GPa and average tensile strength 5.1 MPa), the heterogeneous PLLA/PCL membrane should have potential applications in the field of bone regeneration.

Hierarchical porous silk fibroin/poly(L-lactic acid) fibrous membranes towards vascular scaffolds.

Fibrous membranes played an important role to prepare tubular scaffolds for muscular artery regeneration. In this study, a strategy has been developed to combine silk fibroin (SF) with highly porous electrospun poly(L-lactic acid) (PLLA) fibrous membrane towards vascular scaffolds. After PLLA fibres were electrospun and collected, they were immersed into acetone to generate a porous structure with ultra-high surface area. While the pores on PLLA fibres were fulfilled with SF solution and dried, SF was coated uniformly and tightly on PLLA fibres. A multi-layer tubular structure of the tunica media was simulated by winding and stacking a strip of electrospun fibrous membrane. In vitro viability and morphology studies of A7r5 smooth muscle cells were undertaken for up to 14 days. Because the hydrophilicity of SF/PLLA composite fibres were improved dramatically, it had a positive effect on cell adhesion rate (97%) and proliferation (64.4%). Moreover, good cell morphology was observed via a multiphoton laser confocal microscope on SF/PLLA bioactive materials. These results demonstrated that the hierarchical porous SF/PLLA fibrous membranes are promising off-the-shelf scaffolds for muscular artery regeneration.

Ultrafast bone-like apatite formation on highly porous poly(l-lactic acid)-hydroxyapatite fibres.

In order to provide a favourable environment for living bone formation, it is an essential condition to grow bone-like apatite layer at the interface between the tissue-implant and its surrounding tissues. Inspired by the chemical composition and the nano porous structure of natural bones, we developed an ultrafast and accessible route to accelerate effectively the formation of bone-like apatite on the surface of porous poly(l-lactic acid)-hydroxyapatite (PLLA-HA) composite fibres in 5 times simulated body fluid (5SBF). The key of the method lays in successful exposure of HA nanoparticles on the surface of PLLA fibres by acetone treatment of electrospun PLLA-HA nano/micro fibres. The recrystallization of PLLA chains uncovers more HA nanoparticles on the surface of every fibre which provide nucleation sites for calcium and phosphate ions. After only 2 h of immersing in 5SBF, a full layer of apatite completely covered on the surface of porous PLLA-HA fibres. The results indicate that HA nanoparticles on porous fibre surface can accelerate the kinetic deposition of apatite on fibre surface. Biological in vitro cell culture with human osteoblast-like cell for up to 7 days demonstrates that the incorporation of HA nanoparticles on the surface of porous PLLA fibrous membranes leads to significant enhance osteoblast adhesion and proliferation. The route can open avenues for development of fibrous PLLA biomaterials for hard tissue repair and substitution.