Page 64 - IJB-7-4
        P. 64
     Filament Structure, 3D printing, Bone Repair Scaffolds
               Investigation  of structural resorption behavior of biphasic   83.  Wang  H,  Li  Y,  Zuo  Y,  et  al.,  2007,  Biocompatibility
               bioceramics with help of gravimetry, μCT, SEM, and XRD.   and  Osteogenesis  of  Biomimetic  Nano-hydroxyapatite/
               J Biomed Mater Res Part B Appl Biomater, 104:546–53.  Polyamide Composite Scaffolds for Bone Tissue Engineering.
               https://doi.org/10.1002/jbm.b.33419                 Biomaterials, 28:3338–48.
           74.  Sánchez-Salcedo S, Balas F, Izquierdo-Barba I, et al., 2009,      https://doi.org/10.1016/j.biomaterials.2007.04.014
               In Vitro Structural Changes in Porous HA/β-TCP Scaffolds in   84.  Diao  J,  Yang  JO,  Deng  T,  et al.,  2018,  3D-Plotted  Beta-
               Simulated Body Fluid. Acta Biomater, 5:2738–51.     Tricalcium  Phosphate  Scaffolds  with  Smaller  Pore  Sizes
               https://doi.org/10.1016/j.actbio.2009.03.025        Improve  In Vivo Bone Regeneration  and Biomechanical
           75.  Diba M, Camargo WA, Brindisi M, et al., 2017, Composite   Properties  in  a  Critical-Sized  Calvarial  Defect  Rat  Model.
               Colloidal  Gels  Made  of  Bisphosphonate-Functionalized   Adv Healthc Mater, 7:1800441.
               Gelatin  and Bioactive  Glass Particles  for Regeneration  of      https://doi.org/10.1002/adhm.201800441
               Osteoporotic Bone Defects. Adv Funct Mater, 27:1703438.  85.  Shao H, He Y, Fu J, et al., 2016, 3D Printing Magnesium-
               https://doi.org/10.1002/adfm.201703438              doped Wollastonite/β-TCP Bioceramics Scaffolds with High
           76.  Jakus AE, Rutz AL, Jordan SW, et al., 2016, Hyperelastic\  Strength and Adjustable  Degradation.  J  Eur Ceramic Soc,
               bone\:   A   Highly   Versatile,   Growth   Factor-free,   36:1495–503.
               Osteoregenerative,  Scalable,  and Surgically  Friendly      https://doi.org/10.1016/j.jeurceramsoc.2016.01.010
               Biomaterial. Sci Transl Med, 8:358ra127.        86.  Deng C, Lin R, Zhang M, et al., 2019, Micro/Nanometer-
               https://doi.org/10.1126/scitranslmed. aaf 7704      Structured Scaffolds for Regeneration of Both Cartilage and
           77.  Lei  M,  Qu  X,  Liu  H,  et al., 2019, Programmable   Subchondral Bone. Adv Funct Mater, 29:1806068.
               Electrofabrication  of Porous Janus Films with  Tunable      https://doi.org/10.1002/adfm.201806068
               Janus Balance  for  Anisotropic Cell  Guidance and  Tissue   87.  Wei Y,  Gao  H,  Hao  L,  et al.,  2020,  Constructing  a  Sr2+-
               Regeneration. Adv Funct Mater, 29:1900065.          Substituted   Surface   Hydroxyapatite   Hexagon-Like
               https://doi.org/10.1002/adfm.201900065              Microarray  on  3D-Plotted  Hydroxyapatite  Scaffold  to
           78.  Du Y, Liu H, Qin Y, et al., 2017, Selective Laser Sintering   Regulate   Osteogenic   Differentiation.   Nanomaterials,
               Scaffold  with  Hierarchical  Architecture  and  Gradient   10:1672.
               Composition for Osteochondral Repair In Rabbits.      https://doi.org/10.3390/nano10091672
               Biomaterials, 137:37–48.                        88.  Li X, Yuan Y, Liu L, et al., 2020, 3D Printing of Hydroxyapatite/
               https://doi.org/10.1016/j.biomaterials.2017.05.021.  Tricalcium  Phosphate  Scaffold  with  Hierarchical  Porous
           79.  Zhai  X,  Ruan  C,  Ma  Y,  et al.,  2018,  3D-Bioprinted   Structure for Bone Regeneration. Biodes Manufact, 3:15–29.
               Osteoblast-Laden  Nanocomposite  Hydrogel  Constructs      https://doi.org/10.1007/s42242-019-00056-5
               with  Induced  Microenvironments  Promote  Cell  Viability,   89.  Wang C, Lai J, Li K, et al., 2020, Cryogenic 3D Printing of
               Differentiation, and Osteogenesis both In Vitro and In Vivo.   Dual-delivery  Scaffolds  for  Improved  Bone  Regeneration
               Adv Sci, 5:1700550.                                 with Enhanced Vascularization. Bioact Mater, 6:137–45.
               https://doi.org/10.1002/advs.201700550              https://doi.org/10.1016/j.bioactmat.2020.07.007
           80.  Inzana JA, Olvera D, Fuller SM, et al., 2014, 3D Printing   90.  Pae H, Kang J, Cha J, et al., 2019, 3D-printed Polycaprolactone
               of Composite Calcium Phosphate and Collagen Scaffolds for   Scaffold  Mixed  with  β‐Tricalcium  Phosphate  as  a  Bone
               Bone Regeneration. Biomaterials, 35:4026–34.        Regenerative Material in Rabbit Calvarial Defects. J Biomed
               https://doi.org/10.1016/j.biomaterials.2014.01.064  Mater Res Part B Appl Biomater, 107:1254–63.
           81.  Li  X,  Zou  Q,  Chen  H,  et  al., 2019,  In Vivo Changes of      https://doi.org/10.1002/jbm.b.34218
               Nanoapatite  Crystals During Bone Reconstruction  and the   91.  Shao H, Ke X, Liu A, et al., 2017, Bone Regeneration in 3D
               Differences with Native Bone Apatite. Sci Adv, 5:eaay6484.  Printing Bioactive Ceramic Scaffolds with Improved Tissue/
               https://doi.org/10.1126/sciadv. aay 6484            Material  Interface  Pore  Architecture  in  Thin-wall  Bone
           82.  Montalbano G, Molino G, Fiorilli S, et al., 2020, Synthesis   Defect. Biofabrication, 9:025003.
               and  Incorporation  of  Rod-like  Nano-hydroxyapatite  into      https://doi.org/10.1088/1758-5090/aa663c
               Type  I Collagen  Matrix:  A  Hybrid Formulation  for 3D   92.  Jin ZW, Wu RH, Shen JH, et al., 2018, Nonstoichiometric
               Printing of Bone Scaffolds. J Eur Ceramic Soc, 40:3689–97.  Wollastonite  Bioceramic  Scaffolds  with  Core-shell  Pore
               https://doi.org/10.1016/j.jeurceramsoc.2020.02.018  Struts and  Adjustable Mechanical and Biodegradable
           60                          International Journal of Bioprinting (2021)–Volume 7, Issue 4
     	
