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Table 1 Examples of implantable nanomaterials used in bone repair

From: The advances in nanomedicine for bone and cartilage repair

Material

Fabrication Technique

Cell type/Animal modle

Outcomes

Refs.

Single component

PCL

electrospinning

rMSCs

The electrospun PCL scaffolds provided an environment that supported mineralized tissue formation

[129]

  

electrospinning

hOB cells

A 3D thick scaffold (93% porosity) was fabricated by changing the process parameters and PCL solution characteristics

[132]

  

TISA

mBMSCs

The highly porous (96.4%) TISA scaffold acted as favourable synthetic ECM for functional bone regeneration through a physiological endochondral ossification process

[133]

Nanocomposites

PCL/gelatin

electrospinning

hMSCs

The combination of PCL and gelatin endowed the scaffold with both structural stability of PCL and bioactivity of gelatin, providing a structurally and biochemically improved 3D ECM-like microenvironment for cell infiltration and proliferation within the scaffold

[135]

 

PLLA/PCL

EYA

hESC-MSCs

EYA technology made it possible to construct 3D scaffolds with good mechanical strength and sufficient interconnected micropores in a functionally graded structure

[131]

 

PLA/nβ-TCP

freeze-dry

muscular pockets of rabbits

The nβ-TCP content significantly influenced the in vitro degradation and in vivo osteoconductive properties of the composite scaffolds

[136]

 

gelatin/β-TCP

electrospinning

rBMSCs

The composite scaffolds promoted osteogenic differentiation of BMSCs in vitro and bone regeneration in vivo by activating Ca2+-sensing receptor signaling

[137]

 

nTiO2/PLGA

sonication

hOB cells

The nTiO2/PLGA composites sonicated to have nanometer surface roughness values could improve osteoblast functions

[138]

 

HA–TSF

coaxial electrospinning

MG-63 osteosarcoma cells

The nanocomposite had good biomimetic and mechanical properties and was more effective than pure silk in inducing cell adhesion, proliferation and bone formation

[148]

 

nHA/PLLA

TIPS

none

The incorporation of nHA improved the mechanical properties and protein adsorption of the composite scaffolds while maintaining high porosity and suitable microarchitecture

[149]

 

GelMA-GNP

photo-crosslinking

hADSCs

The hydrogels loaded with GNPs promoted proliferation, differentiation, and ALP activities of hADSCs as they differentiated towards osteoblast cells in dose-dependent manner

[154]

 

Sr-GelMA

short vortex spinning

hMSCs

The addition of Sr nanoparticles greatly enhanced the printability of the composite bioink, and scaffolds bioprinted from it remained stable through 28 days of culture, showing vast MSCs osteogenic differentiation capacity

[156]

 

GelMA/MNPs

photo-crosslinking

hMSCs, MC3T3s

The adjustable mechanical properties of hydrogels could be achieved by controlling the size and concentration of MNPs

[157]

 

PIC/MWCNTs

ultrasonication

rBMSCs

The introduction of MWCNTs into the PIC hydrogel could stimulate the proliferation and osteogenic differentiation of BMSCs

[159]

 

PECE/Collagen/nHA

ultrasonication

cranial defects of New Zealand White rabbits

The hydrogel composite had both injectability and thermo-sensitivity, and showed good capacity to guide bone regeneration, which had great potential in the minimally invasive repair of bone defects

[160]

 

Alginate/gelatin/SiO2

chemical crosslinking

hUMSCs

Biocompatibility and osteogenic ability of the hydrogels were significantly increased with the addition of SiO2

[161]

 

GelMA-G-MBGN

co-crosslinking

MC3T3-E1 cells

This enhanced organic − inorganic hydrogel membrane could maintain localized body fluid environment stability under the premise of promoting vascular regeneration to accelerate bone tissue reconstruction

[163]

 

PNAGA-Clay

physical crosslinking

ROB

The hydrogen bonding of nanoclay contributed to the superior mechanical performances as well as swelling stability of the hydrogels

[164]

 

LPN-GelMA

DW

hBMSCs

Developing a novel light-curable nanocomposite bioink for 3D skeletal regeneration supportive of cell growth and growth factor retention and delivery

[165]

 

CHPOA-PEGSH

chemical crosslinking

mouse calvarial bone defect model

CHPOA/hydrogel was an efficient delivery system for coadministration of FGF18 and BMP2 with the potential to improve the ratio of complete healing of calvarial defects in individual mice

[166]

  1. PCL, poly (ε-caprolactone); rMSCs, rat mesenchymal stem cells; hOB, human osteoblast; TISA, thermally induced self-agglomeration; mBMSCs, mouse bone marrow mesenchymal stem cells; hMSCs, human mesenchymal stem cells; ECM, extracellular matrix; PLLA, poly (L-lactic acid); EYA, electrospinning-based yarn assembly; hESC-MSCs, human embryonic stem cell-derived mesenchymal stem cells; PLA, poly (lactic acid); nβ-TCP, nano-sized β-tricalcium phosphate; nTiO2, nanophase titania; PLGA, poly- (lactide-co-glycolic); HA, hydroxyapatite; TSF, tussah silk fibroin; TIPS, thermally induced phase separation; GelMA, methacrylated gelatin; GNP, gold nanoparticles; hADSCs, human adipose-derived stem cells; ALP, alkaline phosphate; Sr, strontium-carbonate; MNPs, magnetic nanoparticles; MC3T3s, murine-derived preosteoblasts; PIC, polyion complex; MWCNTs, multiwalled carbon nanotubes; PECE, triblock copolymer poly (ethylene glycol)-poly (ε-caprolactone)-poly (ethylene glycol); hUMSCs, human umbilical cord mesenchymal stem cells; PNAGA, poly (N-acryloyl glycinamide); ROB, rat osteoblast; LPN, a synthetic nanoclay, Laponite®; DW, deionised water; CHPOA, acryloyl group-modified cholesterol-bearing pullulan; PEGSH, thiol group-modified polyethylene glycol; FGF18, recombinant human fibroblast growth factor 18; BMP2, recombinant human bone morphogenetic protein 2