Magnesium-based nanoparticles
have shown promise in regenerative
therapies in orthopedics and the cardiovascular system. Here, we set
out to assess the influence of differently functionalized Mg nanoparticles
on the cellular players of wound healing, the first step in the process
of tissue regeneration. First, we thoroughly addressed the physicochemical
characteristics of magnesium hydroxide nanoparticles, which exhibited
low colloidal stability and strong aggregation in cell culture media.
To address this matter, magnesium hydroxide nanoparticles underwent
surface functionalization by 3-aminopropyltriethoxysilane (APTES),
resulting in excellent dispersible properties in ethanol and improved
colloidal stability in physiological media. The latter was determined
as a concentration- and time-dependent phenomenon. There were no significant
effects on THP-1 macrophage viability up to 1.500 μg/mL APTES-coated
magnesium hydroxide nanoparticles. Accordingly, increased media pH
and Mg
2+
concentration, the nanoparticles dissociation
products, had no adverse effects on their viability and morphology.
HDF, ASCs, and PK84 exhibited the highest, and HUVECs, HPMECs, and
THP-1 cells the lowest resistance toward nanoparticle toxic effects.
In conclusion, the indicated high magnesium hydroxide nanoparticles
biocompatibility suggests them a potential drug delivery vehicle for
treating diseases like fibrosis or cancer. If delivered in a targeted
manner, cytotoxic nanoparticles could be considered a potential localized
and specific prevention strategy for treating highly prevalent diseases
like fibrosis or cancer. Looking toward the possible clinical applications,
accurate interpretation of in vitro cellular responses is the keystone
for the relevant prediction of subsequent in vivo biological effects.