This study demonstrates that zoledronate containing hydroxyapatite nanocrystals (HA-ZOL) can be synthesized as a single crystalline phase up to a zoledronate content of about 7 wt% by direct synthesis in aqueous solution, at variance with what previously found for alendronate-hydroxyapatite nanocrystals (HA-AL). On increasing zoledronate incorporation, the length of the coherent crystalline domains and the crystal dimensions of hydroxyapatite decrease, whereas the specific surface area increases. Full profile fitting of the powder X-ray diffraction patterns does not indicate major structural modifications, but an increase of the hydroxyapatite unit cell, on increasing zoledronate content. These data, together with a structural similarity between hydroxyapatite and calcium zoledronate, suggest a preferential interaction between zoledronate and the hydroxyapatite faces parallel to the c-axis direction. Osteoblast-like MG-63 cells and human osteoclasts were cultured on HA-ZOL nanocrystals and as a comparison on HA-AL nanocrystals containing almost the same (about 7 wt%) bisphosphonate amount. The beneficial influence of bisphosphonates on osteoblast proliferation and differentiation is enhanced when the tests are performed in co-cultures. Similarly, the reduction of osteoclast proliferation and the increase of Caspase 3 production are dramatically enhanced in co-cultures, which highlight an even greater influence of HA-ZOL than HA-AL on osteoclast apoptosis. © 2011 Elsevier Ltd.

The effect of zoledronate-hydroxyapatite nanocomposites on osteoclasts and osteoblast-like cells in vitro

Gazzano;
2012

Abstract

This study demonstrates that zoledronate containing hydroxyapatite nanocrystals (HA-ZOL) can be synthesized as a single crystalline phase up to a zoledronate content of about 7 wt% by direct synthesis in aqueous solution, at variance with what previously found for alendronate-hydroxyapatite nanocrystals (HA-AL). On increasing zoledronate incorporation, the length of the coherent crystalline domains and the crystal dimensions of hydroxyapatite decrease, whereas the specific surface area increases. Full profile fitting of the powder X-ray diffraction patterns does not indicate major structural modifications, but an increase of the hydroxyapatite unit cell, on increasing zoledronate content. These data, together with a structural similarity between hydroxyapatite and calcium zoledronate, suggest a preferential interaction between zoledronate and the hydroxyapatite faces parallel to the c-axis direction. Osteoblast-like MG-63 cells and human osteoclasts were cultured on HA-ZOL nanocrystals and as a comparison on HA-AL nanocrystals containing almost the same (about 7 wt%) bisphosphonate amount. The beneficial influence of bisphosphonates on osteoblast proliferation and differentiation is enhanced when the tests are performed in co-cultures. Similarly, the reduction of osteoclast proliferation and the increase of Caspase 3 production are dramatically enhanced in co-cultures, which highlight an even greater influence of HA-ZOL than HA-AL on osteoclast apoptosis. © 2011 Elsevier Ltd.
2012
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Bisphosphonates
C-axis direction
Caspase-3
Co-cultures
Crystal dimensions
Crystalline domains
Direct synthesis
Hydroxyapatite nanocrystals
In-vitro
Osteoblast proliferation
Osteoblast-like cells
Osteoclast
Osteoclast proliferation
Powder X ray diffraction
Preferential interaction
Profile fitting
Single-crystalline
Structural modifications
Structural similarity
Unit cells
Cell culture
Cell death
Cobalt
Crystalline materials
Diffraction
Hydroxyapatite
Nanocomposites
Nanocrystals
X ray diffraction
Apatite
bisphosphonic acid derivative
caspase 3
hydroxyapatite
nanocomposite
nanocrystal
zoledronic acid
article
cell differentiation
cell proliferation
chemical interaction
coculture
controlled study
crystal structure
human
human cell
osteoblast
osteoclast
priority journal
synthesis
X ray diffraction
Alendronate
Cell Differentiation
Cell Proliferation
Cells
Cultured
Diphosphonates
Durapatite
Humans
Imidazoles
Microscopy
Electron
Scanning
Nanocomposites
Nanoparticles
Osteoblasts
Osteoclasts
X-Ray Diffraction
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/250712
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