posted on 2019-11-08, 21:04authored byYan Li, Hang Hao, Zhengyu Zhong, Mengdie Li, Jiaqi Li, Yingying Du, Xiaodan Wu, Jianglin Wang, Shengmin Zhang
Hydroxyapatite
is the main inorganic component of human bone. Synthetic
hydroxyapatite and its different modified forms, which have been shown
to be biocompatible and osteoconductive, have been widely used in
bone tissue engineering. It is still challenging to controllably synthesize
hydroxyapatite with a targeted morphology. In this work, we synthesized
highly crystalline selenium-doped hydroxyapatite nanorods (SeHAN)
via a two-step alcohol thermal method and provided a complete explanation
of the synthesis mechanism. Tracing the crystals obtained from the
solvated phase to the crystal phase with high-resolution microscopy,
the nanorod formation route can be briefly described as follows: as
a basic unit, ∼30 nm amorphous apatite initially formed in
the first step and partly crystallized in early part of the second
step; after a period of alcohol thermal reaction, immature nanorods
appeared, which were composed of nanocrystals; finally, immature nanorods
transformed into single-crystal nanorods through crystallization by
particle attachment. Since few works have focused on the osteogenesis
ability of SeHAN, whose antitumor effect has been widely studied,
we investigated the influences of SeHAN on rat-bone-marrow-resident
mesenchymal stem cells (MSCs). Surprisingly, SeHAN exhibited excellent
biocompatibility for MSCs, enhanced their osteogenic differentiation,
and inhibited their adipogenic differentiation. This work provides
not only a general method to controllably synthesize hydroxyapatite
nanorods/SeHAN but also an insight into understanding the hydroxyapatite
formation mechanism. The current study also highlights the effects
of SeHAN on MSCs that could furnish a significative strategy for manufacturing
functional biomaterials for biomedical applications and tissue engineering
by enhanced ossification and reduced marrow adiposity.