Biopolymers, such as poly(ε-caprolactone), can be easily electrospun to create fibrous scaffolds. It is also possible to control the alignment of the emitted fibres and further manipulate these scaffolds to create 3D yarn structures, which resemble part of the tendon tissue hierarchy. Material properties, such as tensile strength, can be tailored depending on the selection and combination of polymer and solvent used during electrospinning. The scaffolds have been proven to separately support the adhesion and proliferation of equine tendon fibroblasts and human mesenchymal stem cells whilst simultaneously directing cell orientation, which caused their alignment parallel to the underlying fibres. Implantation of scaffolds into the flexor digitorum profundus tendon of mice hindpaws yielded encouraging results with minimal inflammatory reaction and observation of cell infiltration into the scaffold. This research demonstrates the progression of electrospun fibres along the clinical roadmap towards becoming a future medical device for the treatment of tendon injuries. 1. Introduction Electrospinning has become a popular technique in the field of biomaterials and tissue engineering due to the ease at which fibrous scaffolds can be fabricated. The ability to control fibre properties and create 3D structures, with architectures similar to the extracellular matrix, lends itself to a range of tissues, including bone, heart valves, trachea, and tendons [1]. As highly fibrous tissues that repeatedly transfer loads from muscle to bone, tendons are susceptible to wear and tear and spontaneous rupture. Depending on the injury sustained, surgeons can opt to repair the area of damage with autologous tendon tissue. Whilst this is classed as the “gold standard” intervention, it is not without its disadvantages: creation of a secondary site of tissue morbidity arises which can increase the risk of infection and prolong patient rehabilitation time; the ability to source suitable tissue to provide an autograft cannot be guaranteed. Consequently, alternative therapies using biomaterials are being explored. There are a number of commercially available products that aim to repair damaged tendons including Teno Fix manufactured by Ortheon Medical, which is a permanent stainless steel anchor and suture system; Poly-Tape/AchilloCord produced by Xiros (Neoligaments), which is a dense, woven network of nondegradable synthetic polymer; and TissueMend, similar to a number of available devices, which functions as a wrap made of collagen from fetal bovine dermis to be placed around the
References
[1]
L. A. Bosworth and S. Downes, Electrospinning for Tissue Regeneration, Woodhead Publishing, Cambridge, UK, 2011.
[2]
J. Chen, J. Xu, A. Wang, and M. Zheng, “Scaffolds for tendon and ligament repair: review of the efficacy of commercial products,” Expert Review of Medical Devices, vol. 6, no. 1, pp. 61–73, 2009.
[3]
D. G. Wallace and J. Rosenblatt, “Collagen gel systems for sustained delivery and tissue engineering,” Advanced Drug Delivery Reviews, vol. 55, no. 12, pp. 1631–1649, 2003.
[4]
J. Garvin, J. Qi, M. Maloney, and A. J. Banes, “Novel system for engineering bioartificial tendons and application of mechanical load,” Tissue Engineering, vol. 9, no. 5, pp. 967–979, 2003.
[5]
M. Cervellin, L. de Girolamo, C. Bait, M. Denti, and P. Volpi, “Autologous platelet-rich plasma gel to reduce donor-site morbidity after patellar tendon graft harvesting for anterior cruciate ligament reconstruction: a randomized, controlled clinical study,” Knee Surgery, Sports Traumatology, Arthroscopy, vol. 20, no. 1, pp. 114–120, 2012.
[6]
L. A. Bosworth, N. Alam, J. K. Wong, and S. Downes, “Investigation of 2D and 3D electrospun scaffolds intended for tendon repair,” Journal of Materials Science: Materials in Medicine, vol. 24, no. 6, pp. 1605–11614, 2013.
[7]
K. L. Moffat, A. S.-P. Kwei, J. P. Spalazzi, S. B. Doty, W. N. Levine, and H. H. Lu, “Novel nanofiber-based scaffold for rotator cuff repair and augmentation,” Tissue Engineering A, vol. 15, no. 1, pp. 115–126, 2009.
[8]
L. A. Bosworth and S. Downes, “Acetone, a sustainable solvent for electrospinning poly(ε-caprolactone) fibres: effect of varying parameters and solution concentrations on fibre diameter,” Journal of Polymers and the Environment, vol. 20, no. 3, pp. 879–886, 2012.
[9]
L. A. Bosworth, “Electrospinning for tendon regeneration,” in Electrospinning for Tissue Regeneration, L. A. Bosworth and S. Downes, Eds., pp. 148–167, Woodhead Publishing, Cambridge, UK, 2011.
[10]
D. W. Hutmacher, T. Schantz, I. Zein, K. W. Ng, S. H. Teoh, and K. C. Tan, “Mechanical properties and cell cultural response of polycaprolactone scaffolds designed and fabricated via fused deposition modeling,” Journal of Biomedical Materials Research, vol. 55, no. 2, pp. 203–216, 2001.
[11]
M. Sun and S. Downes, “Solvent-cast PCL films support the regeneration of NG108-15 nerve cells,” in International Conference on Smart Materials and Nanotechnology in Engineering, Proceedings of SPIE, July 2007.
[12]
K. Kyriakidou, G. Lucarini, A. Zizzi et al., “Dynamic co-seeding of osteoblast and endothelial cells on 3D polycaprolactone scaffolds for enhanced bone tissue engineering,” Journal of Bioactive and Compatible Polymers, vol. 23, no. 3, pp. 227–243, 2008.
[13]
H. Sun, L. Mei, C. Song, X. Cui, and P. Wang, “The in vivo degradation, absorption and excretion of PCL-based implant,” Biomaterials, vol. 27, no. 9, pp. 1735–1740, 2006.
[14]
L. A. Bosworth, A. Gibb, and S. Downes, “Gamma irradiation of electrospun poly (ε-caprolactone) fibers affects material properties but not cell response,” Journal of Polymer Science B: Polymer Physics, vol. 50, no. 12, pp. 870–876, 2012.