Reinforced Degradable Biocomposite by Homogenously Distributed Functionalized Nanodiamond Particles

The treatment of bone defects is facing the situation of lacking donations for autotransplantation. As a valid approach, scaffold-based tissue engineering combines the construction of well-defined porous scaffolds with advanced cell culturing technology to guide tissue regeneration. The role for the scaffold is to provide a suitable environment with a sufficient mechanical stiffness, supports for cell attachment, migration, nutrients and metabolite transport and space for cell remodeling and tissue regeneration. The random copolymers poly(L-lactide-co-ɛ-caprolactone) (poly(LLA-co-CL)) and poly(L-lactide-co-1,5-dioxepan-2-one) (poly(LLA-co-DXO)) have been successfully incorporated into 3D porous scaffolds to induce specific interactions with cells and direct osteogenic cell differentiation. In this thesis, these scaffolds have been modified in chemical and physical ways to map and understand requirements for bone regeneration. Scaffold functionalities and properties, such as hydrophilicity, stiffness, size/shape, and reproducibility, were studied. The hydrophilicity was varied by adding 3–20 % (w/w) Tween 80 to poly(LLA-co-CL) and poly(LLA-co-DXO) respectively, which resulted in contact angles from 35° to 15°. With 3 % Tween 80, the resultant mechanical and thermal properties were similar to pristine polymer materials. Tween 80 did not significantly influence cell attachment or proliferation but did stimulate the mRNA expression of osteogenetic markers. The surface functionality and mechanical properties were altered by introducing nanodiamond particles (n-DP) into poly(LLA-co-CL) scaffolds by means of surface physisorption or hybrid blending. Scaffold with n-DP physisorbed showed improved cell attachment, differentiation, and bone reformation. Hybrid n-DP/poly(LLA-co-CL) composites were obtained by direct blending of polylactide modified n-DP (n-DP-PLA) with poly(LLA-coCL). The n-DP-PLA was prepared by sodium hydride-mediated anionic polymerization using n-DP as the initiator. Prepared n-DP-PLA could be dispersed homogenously in organic solvents and blended with poly(LLA-coCL) solution. The n-DP-PLA particles were homogenously distributed in the composite material, which significantly improved mechanical properties. For comparison, the addition of benzoquinone-modified n-DP (n-DP-BQ) did not reinforce poly(LLA-co-CL). This indicated the importance of specific surface grafting, which determined different particle-polymer interactions. For the treatment of critical size defects, a large porous poly(LLA-co-CL) scaffold (12.5 mm diameter × 25 mm thickness) was developed and produced by molding and salt-leaching methods. The large porous scaffolds were evaluated in a scaffold-customized perfusion-based bioreactor system. It was obvious that the scaffold could support improved cell distribution and support the stimulation of human mesenchymal stem cell (hMSC) especially with dynamic flow in a bioreactor. To improve the scaffolding technique, a three-dimensional fiber deposition (3DF) technique was employed to build layer-based scaffolds. Poly(LLA-coCL) scaffolds produced by the 3DF method showed enhanced mechanical properties and a homogeneous distribution of human osteoblasts (hOBs) in the scaffolds. Although poly(LLA-co-CL) was thermally degraded, the degradation did not influence the scaffold mechanical properties. Based on the computerized design, a 3DF scaffold of amorphous copolymer poly(LLAco-CL) provides high-precision control and reproducibility. In summary, the design of porous scaffolds is one of the essential factors in tissue engineering as to mimicking the intrinsic extracellular environment. For bone tissue engineering, an optimized scaffold can maintain a contact angle greater than 35 degrees. Pristine or modified n-DP, introduced as an additive by surface physisorption or direct blending, can improve scaffold mechanical properties and cell response. Various sizes of scaffolds can be easily produced by a mold-mediated salt-leaching method. However, when 100 % reproducibility is required, the 3DF method can be used to create customizable scaffolds.

[1]  Yang Sun,et al.  Release and bioactivity of bone morphogenetic protein-2 are affected by scaffold binding techniques in vitro and in vivo. , 2015, Journal of controlled release : official journal of the Controlled Release Society.

[2]  A. Albertsson,et al.  Surfactant as a critical factor when tuning the hydrophilicity in three-dimensional polyester-based scaffolds: impact of hydrophilicity on their mechanical properties and the cellular response of human osteoblast-like cells. , 2014, Biomacromolecules.

[3]  J. Lorens,et al.  Mesenchymal stem cells induce endothelial cell quiescence and promote capillary formation , 2014, Stem Cell Research & Therapy.

[4]  E. Ōsawa,et al.  Multi-protein Delivery by Nanodiamonds Promotes Bone Formation , 2013, Journal of dental research.

[5]  Mari Sasao,et al.  N-Cadherin is a prospective cell surface marker of human mesenchymal stem cells that have high ability for cardiomyocyte differentiation. , 2013, Biochemical and biophysical research communications.

[6]  Yang Sun,et al.  Biological effects of functionalizing copolymer scaffolds with nanodiamond particles. , 2013, Tissue engineering. Part A.

[7]  Antonios Kontsos,et al.  Maximizing Young's modulus of aminated nanodiamond-epoxy composites measured in compression , 2012 .

[8]  Yang Sun,et al.  Degradable amorphous scaffolds with enhanced mechanical properties and homogeneous cell distribution produced by a three-dimensional fiber deposition method. , 2012, Journal of biomedical materials research. Part A.

[9]  A. Krueger,et al.  Functionality is Key: Recent Progress in the Surface Modification of Nanodiamond , 2012 .

[10]  Y. Jeng,et al.  In situ de-agglomeration and surface functionalization of detonation nanodiamond, with the polymer used as an additive in lubricant oil , 2011 .

[11]  A. Krueger,et al.  Beyond the shine: recent progress in applications of nanodiamond , 2011 .

[12]  Masaru Kotera,et al.  Poly(vinyl alcohol) Nanocomposites with Nanodiamond , 2011 .

[13]  Yury Gogotsi,et al.  Fluorescent PLLA-nanodiamond composites for bone tissue engineering. , 2011, Biomaterials.

[14]  Yury Gogotsi,et al.  The properties and applications of nanodiamonds. , 2011, Nature nanotechnology.

[15]  Jang‐Kyo Kim,et al.  Nanodiamond/poly (lactic acid) nanocomposites: Effect of nanodiamond on structure and properties of poly (lactic acid) , 2010 .

[16]  Fernando Guiberteau,et al.  Improving the compressive strength of bioceramic robocast scaffolds by polymer infiltration. , 2010, Acta biomaterialia.

[17]  K. Purtov,et al.  Nanodiamonds as Carriers for Address Delivery of Biologically Active Substances , 2010, Nanoscale research letters.

[18]  A. Albertsson,et al.  Osteogenic Differentiation by Rat Bone Marrow Stromal Cells on Customized Biodegradable Polymer Scaffolds , 2010 .

[19]  Sofia Målberg,et al.  Design of resorbable porous tubular copolyester scaffolds for use in nerve regeneration. , 2009, Biomacromolecules.

[20]  A. Krueger,et al.  Deagglomeration and functionalisation of detonation nanodiamond with long alkyl chains , 2008 .

[21]  A. P. Korobko,et al.  Nanodiamonds as modifier of ethylene-1-octene copolymer structure and properties , 2007 .

[22]  M. Ozawa,et al.  Preparation and Behavior of Brownish, Clear Nanodiamond Colloids , 2007 .

[23]  S. Monteiro,et al.  Diamond-Epoxy Composites , 2007 .

[24]  Anna C. Balazs,et al.  Nanoparticle Polymer Composites: Where Two Small Worlds Meet , 2006, Science.

[25]  C. Huck,et al.  Strong binding of bioactive BMP-2 to nanocrystalline diamond by physisorption. , 2006, Biomaterials.

[26]  K. Jacob,et al.  Characterization of Polymer Nanocomposite Interphase and Its Impact on Mechanical Properties , 2006 .

[27]  M. Ozawa,et al.  Unusually tight aggregation in detonation nanodiamond: Identification and disintegration , 2005 .

[28]  T. Kiyono,et al.  Combination of hTERT and bmi-1, E6, or E7 Induces Prolongation of the Life Span of Bone Marrow Stromal Cells from an Elderly Donor without Affecting Their Neurogenic Potential , 2005, Molecular and Cellular Biology.

[29]  E. Agostinelli,et al.  Specific immobilization of laccase onp-benzoquinone-activated supports , 1990, Biology of Metals.

[30]  Peter X Ma,et al.  Structure and properties of nano-hydroxyapatite/polymer composite scaffolds for bone tissue engineering. , 2004, Biomaterials.

[31]  Jung-Ki Park,et al.  Morphology and hydrolysis of PCL/PLLA blends compatibilized with P(LLA-co-epsilon CL) or P(LLA-b-epsilon CL) , 2002 .

[32]  J. Porath,et al.  Covalent attachment of proteins to polysaccharide carriers by means of benzoquinone. , 1975, Biochimica et biophysica acta.

[33]  G. Wegner,et al.  Investigation of the structure of solution grown crystals of lactide copolymers by means of chemical reactions , 1973 .