Page 287 - Advances in Biomechanics and Tissue Regeneration

REFERENCES 285

[27] G. Gao, et al., Inkjet-bioprinted acrylated peptides and PEG hydrogel with human mesenchymal stem cells promote robust bone and cartilage
formation with minimal printhead clogging, Biotechnol. J. 10 (10) (2015) 1568–1577.
[28] C.M. Livoti, J.R. Morgan, Self-assembly and tissue fusion of toroid-shaped minimal building units, Tissue Eng. A 16 (6) (2010) 2051–2061.
[29] D.F. Duarte Campos, et al., The stiffness and structure of three-dimensional printed hydrogels direct the differentiation of mesenchymal stromal
cells toward adipogenic and osteogenic lineages, Tissue Eng. A 21 (3–4) (2014) 740–756.
[30] T. Xu, et al., Inkjet printing of viable mammalian cells, Biomaterials 26 (1) (2005) 93–99.
[31] K.K. Lai, R. Renneberg, W.C. Mak, High efficiency single-step biomaterial-based microparticle fabrication via template-directed supramolecular
coordination chemistry, Green Chem. 18 (6) (2016) 1715–1723.
[32] I.T. Ozbolat, H. Chen, Y. Yu, Development of ‘Multi-arm Bioprinter’ for hybrid biofabrication of tissue engineering constructs, Robot. Comput.
Integr. Manuf. 30 (3) (2014) 295–304.
[33] Y. Zhang, Y. Yu, I.T. Ozbolat, Direct bioprinting of vessel-like tubular microfluidic channels, J. Nanotechnol. Eng. Med. 4 (2) (2013) 020902.
[34] H. Gudapati, et al., Alginate gelation-induced cell death during laser-assisted cell printing, Biofabrication 6 (3) (2014) 035022.
[35] B. Guillotin, et al., Laser assisted bioprinting of engineered tissue with high cell density and microscale organization, Biomaterials 31 (28) (2010)
7250–7256.
[36] P. Fratzl, Collagen: structure and mechanics, an introduction, in: Collagen, Springer, 2008, pp. 1–13.
[37] C.M. Smith, et al., Three-dimensional bioassembly tool for generating viable tissue-engineered constructs, Tissue Eng. 10 (9–10) (2004)
1566–1576.
[38] A. Skardal, et al., Bioprinted amniotic fluid-derived stem cells accelerate healing of large skin wounds, Stem Cells Transl. Med. 1 (11) (2012)
792–802.
[39] X. Wang, et al., Generation of three-dimensional hepatocyte/gelatin structures with rapid prototyping system, Tissue Eng. 12 (1) (2006) 83–90.
[40] M. Mesa, et al., Morphology and porosity characteristics control of SBA-16 mesoporous silica. Effect of the triblock surfactant Pluronic F127
degradation during the synthesis, Solid State Sci. 7 (8) (2005) 990–997.
[41] S. Wang, et al., Receptor-mediated drug delivery systems targeting to glioma, Nanomaterials 6 (1) (2015) 3.
[42] W. Wu, A. DeConinck, J.A. Lewis, Omnidirectional printing of 3D microvascular networks, Adv. Mater. 23 (24) (2011) H178–H183.
[43] D. Hanjaya-Putra, et al., Controlled activation of morphogenesis to generate a functional human microvasculature in a synthetic matrix, Blood
118 (2011) 804–815.
[44] J.W. Nichol, et al., Cell-laden microengineered gelatin methacrylate hydrogels, Biomaterials 31 (21) (2010) 5536–5544.
[45] Y.C. Chen, et al., Functional human vascular network generated in photocrosslinkable gelatin methacrylate hydrogels, Adv. Funct. Mater.
22 (10) (2012) 2027–2039.
[46] R.-Z. Lin, et al., Transdermal regulation of vascular network bioengineering using a photopolymerizable methacrylated gelatin hydrogel,
Biomaterials 34 (28) (2013) 6785–6796.
[47] E. Hoch, et al., Chemical tailoring of gelatin to adjust its chemical and physical properties for functional bioprinting, J. Mater. Chem. B 1 (41)
(2013) 5675–5685.
[48] D.S. Benoit, A.R. Durney, K.S. Anseth, Manipulations in hydrogel degradation behavior enhance osteoblast function and mineralized tissue
formation, Tissue Eng. 12 (6) (2006) 1663–1673.
[49] B.-H. Jo, et al., Three-dimensional micro-channel fabrication in polydimethylsiloxane (PDMS) elastomer, J. Microelectromech. Syst. 9 (1) (2000)
76–81.
[50] T.J. Hinton, et al., 3D printing PDMS elastomer in a hydrophilic support bath via freeform reversible embedding, ACS Biomater. Sci. Eng. 2 (10)
(2016) 1781–1786.
[51] V. Ozbolat, et al., 3D printing of PDMS improves its mechanical and cell adhesion properties, ACS Biomater. Sci. Eng. 4 (2) (2018) 682–693.
[52] C.S. O’Bryan, et al., Self-assembled micro-organogels for 3D printing silicone structures, Sci. Adv. 3 (5) (2017) e1602800.
[53] J. Black, G. Hastings, Handbook of Biomaterials Properties, Chapman and Hall, London, 1998.
[54] R. Yoda, Elastomers for biomedical applications, J. Biomater. Sci. Polym. Ed. 9 (6) (1998) 561–626.
[55] J.E. Puskas, Y. Chen, Biomedical application of commercial polymers and novel polyisobutylene-based thermoplastic elastomers for soft tissue
replacement, Biomacromolecules 5 (4) (2004) 1141–1154.
[56] R.R. De Nicola, Permanent artificial (silicone) urethra, J. Urol. 63 (1) (1950) 168–172.
[57] W.E. Neville, P.J. Bolanowski, H. Soltanzadeh, Prosthetic reconstruction of the trachea and carina, J. Thorac. Cardiovasc. Surg. 72 (4) (1976)
525–538.
[58] S.V. Gohil, et al., Chapter 8: Polymers and composites for orthopedic applications, in: S. Bose, A. Bandyopadhyay (Eds.), Materials for Bone
Disorders, Academic Press, 2017, pp. 349–403.
[59] V.L. Gott, D.E. Alejo, D.E. Cameron, Mechanical heart valves: 50 years of evolution, Ann. Thorac. Surg. 76 (6) (2003) S2230–S2239.
[60] R.J. Thomas, A model for cochlear implant electrode insertion and force evaluation: results with a new electrode design and insertion technique,
Laryngoscope 115 (8) (2005) 1325–1339.
[61] S. Kalousdian, M.S. Karlan, M.A. Williams, Silicone elastomer cerebrospinal fluid shunt systems, Neurosurgery 42 (4) (1998) 887–892.
[62] J. Curtis, A. Colas, Chapter II.5.18: Medical applications of silicones, in: B.D. Ratner, et al. (Eds.), Biomaterials Science, third ed., Academic Press,
2013, pp. 1106–1116.
[63] O. Cuisnier, et al., Surgical and/or endoscopic treatment of acquired tracheal stenosis in adult patients, Ann. Otolaryngol. Chir. Cervicofac.
121 (1) (2004) 3–13.
[64] E.A. Weymuller, Laryngeal injury from prolonged endotracheal intubation, Laryngoscope 98 (1988) 1–15.
[65] J.L. Stauffer, D.E. Olson, T.L. Petty, Complications and consequences of endotracheal intubation and tracheotomy. A prospective study of 150
critically ill adult patients, Am. J. Med. 70 (1) (1981) 65–76.
[66] H.A. Gaissert, R.H. Lofgren, H.C. Grillo, Upper airway compromise after inhalation injury. Complex strictures of the larynx and trachea and
their management, Ann. Surg. 218 (5) (1993) 672–678.
[67] K.M. Greven, et al., Distinguishing tumor recurrence from irradiation sequelae with positron emission tomography in patients treated for larynx
cancer, Int. J. Radiat. Oncol. Biol. Phys. 29 (4) (1994) 841–845.

II. MECHANOBIOLOGY AND TISSUE REGENERATION