Abstract
A titanium (Ti)-adhesive nanoparticle is developed as a surface-releasing system for dual osteogenic growth factors. The Ti-adhesive nanoparticle is prepared by self-assembly of a poly(L-lactide-co-glycolide) (PLGA)-grafted hyaluronic acid (HA) copolymer, followed by conjugation of catechol groups on nanoparticle surfaces. The nanoparticles consist of Ti-adhesive peripheral catechol groups, anionic HA shells, and hydrophobic PLGA inner cores. The immobilization of the nanoparticles onto Ti substrates is successfully verified using various analytical tools including field-emission scanning electron microscopy (Fe-SEM), contact angle measurement, and X-ray photoelectron spectroscopy (XPS). Positively charged dual growth factors, bone morphogenetic protein-2 (BMP-2) and insulin-like growth factor-1 (IGF-1) are readily loaded onto the negatively charged HA shells of surface-immobilized nanoparticles, which is confirmed by fluorescence microscopy. The Ti substrates with dual growth factor-loaded nanoparticle-immobilized nanoparticles remarkably promote the attachment, proliferation, spreading, and alkaline phosphatase (ALP) activity of human adipose-derived stem cells (hADSCs). Titanium-adhesive nanoparticles, that can be strongly immobilized on Ti surfaces and release dual osteogenic growth factors, are developed as a novel surface-releasing system. The Ti substrates with dual growth factor-loaded nanoparticle-immobilized nanoparticles remarkably promote the attachment, proliferation, spreading, and alkaline phosphatase activity of human adipose-derived stem cells.
| Original language | English |
|---|---|
| Pages (from-to) | 496-507 |
| Number of pages | 12 |
| Journal | Macromolecular Bioscience |
| Volume | 14 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Apr 2014 |
Keywords
- adhesive nanoparticles
- bone morphogenetic protein-2
- controlled release
- insulin-like growth factor-1
- surface treatment
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