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Table 2 The scaffolds made of graphene family materials and other synthetic or bio-polymers

From: Graphene Family Materials in Bone Tissue Regeneration: Perspectives and Challenges

Graphene family materials

Synthetic or bio-polymers

Fabrication methods

The improvement of physical or mechanical properties

Key results of experiments in vitro

Key results of experiments in vivo

Ref.

GO

PCL

Electrospinning process

Highly porous nature; an increase in tensile strength, elongation and Young’s modulus

Better biological characteristics with high cell viability

 

[80]

rGO

Macro–mesoporous bioactive glass (MBG); osteoblast-specific aptamer (AP)

Sol–gel method

Macroporous structure with fully interconnected open pores; excellent mechanical properties with a Young’s modulus of ~ 80 kPa

Accelerated the osteogenic differentiation of rat osteoblasts by up-regulating the mRNA expression level of four osteoblast markers sinificantly.

In the large bone defects of the rat femurs, the new bone appeared both peripherally and centrally in rGO-MBG-AP scaffold.

[160]

rGO

Polypyrrole (PPY); casein phosphopeptide (CPP)

Electrostatic self-assembly method

Excellent hydrophilic property and water uptake performance

Promoted the rapid formation of hydroxyapatite in the biomimetic mineralization; enhanced the adhesion, proliferation and osteogenic differentiation of MC3T3-E1 cells.

 

[161]

rGO

PPY; HA

Electrostatic layer-bylayer assembly strategy; biomimetic mineralization

Better mechanical property with desired configuration, high specific surface area and large surface roughness.

Enhanced MC3T3-E1 cells adhesion and proliferation.

 

[162]

GO

Poly(3-hydroxybutyrate-co-4-hydroxybutyrate)

Electrospinning technique

Reduced the fiber diameter and enhanced porosity, hydrophilicity and mechanical properties of the scaffolds.

Improved cellular performance, and osteogenic differentiation in vitro.

Promoted osteogenesis and rapidly increased bone volume even at an early stage.

[163]

GO

Cellulose acetate (CA); nanofibrous

Electrospinning technique

Increased the Young’s modulus of the nanofibers in a GO dose-dependent manner

Facilitated adhesion and proliferation of BMSCs on the scaffolds; accelerated biomineralization; induced osteogenic differentiation of BMSCs

 

[164]

Graphene oxide carboxymethylation (cGO)

HA; silk fibroin (SF)

Biomimetic mineralization and simply mix

Higher compressive strength and compressive modulus, respectively

Stimulated BMSCs adhesion and proliferation, ALP secretion and mineral deposition more strongly

 

[165]

rGO

Zinc silicate (ZS); calcium silicate

Two-step spin-coating method

Increased annealing temperature

Suppressed the receptor activator of nuclear factor-κB-ligand-induced osteoclastic differentiation of mouse leukemic monocyte macrophages

 

[166]

rGO

PDMS

Dipped and dried

Good mechanical strength and with pore sizes ranging from 10 to 600 um

Accelerated growth and differentiation of human adipose stem cells to an osteogenic cell lineage

 

[167]

GO

Nano-HA; collagen; PLGA

Freeze-drying method

Improved the hydrophilicity and reinforced their mechanical strength; increased Young’s modulus (10.20 ± 1.28 GPa)

Enhanced cell adhesion and proliferation of MC3T3-E1

 

[168]

GO

Gelatin hydroxyapatite matrix

Freeze-drying method

Less brittleness

Induced osteogenic differentiation of human adipose derived mesenchymal stem cells without chemical inducer

 

[169]

Pristine graphene

PCL

3D printing

Increased hydrophilicity of the surface

Enhanced cell viability and proliferation

 

[170]

GO multi-walled carbon nanotube oxides (MWCNTO)

Poly (d, l-lactic acid) (PDLLA)

MWCNTO-GO was prepared via oxygen plasma etching (OPE)

High mechanical performance (~ 600 MPa)

Allowed for MG-63 cells interactions and the formation of mineralized matrix significantly facilitated osteoblast ALP activity

Superior influence on bone cell activity, promoting greater new bone formation

[171]

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