Solid-state 31 P and 13 C magic angle spinning (MAS) NMR spectra were used to characterize pure bisphosphonates and also bisphosphonates adsorbed on hydroxyapatite. Four geminal bisphosphonates, including the clinically used compounds ethane-1-hydroxy-1,1-diphosphonic acid, 3-amino-1-hydroxypropane-
Revisiting silicate substituted hydroxyapatite by solid-state NMR
✍ Scribed by G. Gasquères; C. Bonhomme; J. Maquet; F. Babonneau; S. Hayakawa; T. Kanaya; A. Osaka
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 288 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2109
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✦ Synopsis
Abstract
Silicon‐substituted hydroxyapatite (Si‐HAp) has shown promising properties such as high‐bone remodeling around implants. So far, the techniques used for the structural characterization of the Si‐HAp have given indirect evidence of the presence of silicon inside the structure (by X‐ray and neutron diffraction). In this paper, we focus on Si‐HAp derivatives obtained by a precipitation method (widely described in the literature). We demonstrate here by solid‐state NMR spectroscopy that only a fraction of the silicon atoms are incorporated into the HAp lattice in the form of Q^0^ (SiO~4~^4−^) species, for 4.6 wt% Si‐HAp. A large amount of silicate units are located outside the HAp structure and correspond to silica‐gel units. All results were established through ^29^Si MAS, ^1^H →^29^Si CP MAS and T~1~ρ(^1^H) edited ^1^H →^29^Si CP MAS experiments. This last pulse scheme acted as a powerful editing sequence, leading to unambiguous spectroscopic conclusions, concerning the location of the SiO~4~^4−^ moieties. Copyright © 2008 John Wiley & Sons, Ltd.
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