Application of layered poly (L-lactic acid) cell free scaffold in a rabbit rotator cuff defect model

<p>Abstract</p> <p>Background</p> <p>This study evaluated the application of a layered cell free poly (L-lactic acid) (PLLA) scaffold to regenerate an infraspinatus tendon defect in a rabbit model. We hypothesized that PLLA scaffold without cultivated cells would lead to regeneration of tissue with mechanical properties similar to reattached infraspinatus without tendon defects.</p> <p>Methods</p> <p>Layered PLLA fabric with a smooth surface on one side and a pile-finished surface on the other side was used. Novel form of layered PLLA scaffold was created by superimposing 2 PLLA fabrics. Defects of the infraspinatus tendon were created in 32 rabbits and the PLLA scaffolds were transplanted, four rabbits were used as normal control. Contralateral infraspinatus tendons were reattached to humeral head without scaffold implantation. Histological and mechanical evaluations were performed at 4, 8, and 16 weeks after operation.</p> <p>Results</p> <p>At 4 weeks postoperatively, cell migration was observed in the interstice of the PLLA fibers. Regenerated tissue was directly connected to the bone composed mainly of type III collagen, at 16 weeks postoperatively. The ultimate failure load increased in a time-dependent manner and no statistical difference was seen between normal infraspinatus tendon and scaffold group at 8 and 16 weeks postoperatively. There were no differences between scaffold group and reattach group at each time of point. The stiffness did not improve significantly in both groups.</p> <p>Conclusions</p> <p>A novel form of layered PLLA scaffold has the potential to induce cell migration into the scaffold and to bridge the tendon defect with mechanical properties similar to reattached infraspinatus tendon model.</p

Highly Water Repellent but Highly Adhesive Surface with Segregation of Poly(ethylene oxide) Side Chains

Polymer surfaces were modified using methacrylate terpolymers containing both perfluoroalkyl (R_<i>f</i>) groups and poly­(ethylene oxide) (PEO) as side chains in the same molecule. The structure and properties of the modified surfaces were evaluated using X-ray photoelectron spectroscopy and by measuring the dynamic contact angles and 90° peel strength. It was found that not only R_<i>f</i> groups but also PEO side chains were segregated on the surface being against the order of the surface free energy. The terpolymer modified surface is hydrophobic in air because R_<i>f</i> groups are predominant, but it becomes hydrophilic in water because the surface is covered with PEO side chains. This response to the environment is rapid and reversible. The modified surface showed high water repellency because of the surface R_<i>f</i> groups and high adhesive strength because of the side chains

Change in the Crystallite Orientation of Poly(ethylene oxide)/Cellulose Nanofiber Composite Films

The crystallite orientation and crystallographic domain structure of poly­(ethylene oxide) (PEO) in cellulose nanofiber-incorporated (CNF-incorporated) PEO films developed for packaging materials were observed using wide-angle X-ray diffraction for different CNF filling ratios. When a CNF filling ratio of <10 wt % was used, the molecular chains in the PEO crystallite region were oriented in a direction perpendicular to the surface of the film; however, when the ratio was >50 wt %, the PEO molecular chains were oriented in a direction parallel to the surface of the film. The fiber axis of the CNFs became parallel to the surface of the PEO/CNF composite film when the filling ratio was >25 wt %. The change in the orientation of the PEO crystals occurred because increasing the amount of CNF in the composite films decreased the space in which the PEO could be crystallized. Furthermore, the hydrogen bonds between the PEO and the CNF may behave as crystallization nuclei for the PEO. Our results thus pave the way toward the development of packaging materials that are more impermeable to gases than the current materials

Change in the Crystallite Orientation of Poly(ethylene oxide)/Cellulose Nanofiber Composite Films

The crystallite orientation and crystallographic domain structure of poly­(ethylene oxide) (PEO) in cellulose nanofiber-incorporated (CNF-incorporated) PEO films developed for packaging materials were observed using wide-angle X-ray diffraction for different CNF filling ratios. When a CNF filling ratio of <10 wt % was used, the molecular chains in the PEO crystallite region were oriented in a direction perpendicular to the surface of the film; however, when the ratio was >50 wt %, the PEO molecular chains were oriented in a direction parallel to the surface of the film. The fiber axis of the CNFs became parallel to the surface of the PEO/CNF composite film when the filling ratio was >25 wt %. The change in the orientation of the PEO crystals occurred because increasing the amount of CNF in the composite films decreased the space in which the PEO could be crystallized. Furthermore, the hydrogen bonds between the PEO and the CNF may behave as crystallization nuclei for the PEO. Our results thus pave the way toward the development of packaging materials that are more impermeable to gases than the current materials