Editorial Type:
Article Category: Research Article
 | 
Online Publication Date: 10 Dec 2024

Regulation of Osteogenic and Angiogenic Markers in Alkali-Treated Titanium for Hard Tissue Engineering Applications

MS,
MS,
DDS,
PhD, and
PhD
Page Range: 636 – 643
DOI: 10.1563/aaid-joi-D-23-00187
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Titanium (Ti) and Ti alloys are of great interest in bone and dental tissue engineering applications due to their biocompatibility, corrosion resistance, and close mechanical properties to natural bone. However, the formation of fibrous tissue prevents osteointegration and results in implant loosening. Thus, physical and chemical methods are used to improve the surface properties of Ti. This study aimed to understand the role of alkali treatment conditions, including alkali medium concentration, temperature, rotation speed, and post heat treatment. Our results show that alkali treatment using 5 and 10 molar sodium hydroxide (NaOH) solution allows the formation of web-like microstructure. However, a higher concentration of 15 molar resulted in cracks along the surface. Interaction between the human fetal osteoblast cells and Ti samples showed that heat treatment is necessary for increased cellular proliferation, which was not significantly different at later time points compared with the polished Ti. Alkali heat treatment did not induce inflammatory reactions at later time points. It showed an increase in vascular endothelial growth factor, osteoprotegerin/nuclear factor kappa-Β ligand ratio, and osteocalcin expression, which is evidence for accelerated osteoblast cell maturation and bone remodeling in surface-modified samples. Together, these data show that alkali treatment using 5 or 10 molar of NaOH followed by heat treatment may have a therapeutic effect and assist with bone tissue integration with Ti implant.

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Figure 1.
Figure 1.

Surface morphology of samples treated with 5M NaOH and (a) 40°C, 30 rpm; (b) 60°C, 0 rpm; and (c): 60°C, 30 rpm. (d) Sample (c) after heat treatment.


Figure 2.
Figure 2.

Surface morphology of samples treated with 10 M NaOH and (a) 40°C, 0 rpm; (b) 40°C, 30 rpm; (c) 40°C, 60 rpm; (d) 60°C, 0 rpm; (e) 60°C, 30 rpm; and (f) 60°C, 60 rpm. (g) Sample f after heat treatment.


Figure 3.
Figure 3.

Cell growth on polished and surface-treated Ti samples at days 3, 6, and 8 of culture, measured by MTT assay.


Figure 4.
Figure 4.

Expression of IL-6 and TNFα on polished and surface-treated Ti samples at days 3, 6, and 8 of culture, measured by RT-qPCR. *A low level of RNA yield.


Figure 5.
Figure 5.

Expression of ALP-1, OCN, RANKL, OPG, VEGF, and COL1A-1 on polished and surface-treated Ti samples measured by RT-qPCR on days 3, 6, and 8 of culture. *A low level of RNA yield.


Contributor Notes

Corresponding author, e-mail: paige.bothwell@fresenius-kabi.com, svahabzadeh@niu.edu
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