2011
DOI: 10.1016/j.jchromb.2011.04.035
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Surface energetics of bone mineral and synthetic hydroxyapatite using inverse gas chromatography

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Cited by 13 publications
(10 citation statements)
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References 16 publications
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“…Figure 3(c) has illustrated the transition that CAP nanoparticles underwent during desiccation: aggregation into compact microsized blocks. The naturally rough surface of CAP particles exhibits topographic irregularities on the atomic scale,38, 39 which does not only favor protein adsorption,40 osteoblast differentiation,41 and expression of osteogenic markers42 but also causes high levels of adhesion upon contact, promoting facile formation and retention of stable aggregates even under relatively intensive agitations in the solution. This propensity of the particles to form aggregates subsequently stable in solution was used as the primary mechanism for loading the powders with small organic molecules.…”
Section: Resultsmentioning
confidence: 99%
“…Figure 3(c) has illustrated the transition that CAP nanoparticles underwent during desiccation: aggregation into compact microsized blocks. The naturally rough surface of CAP particles exhibits topographic irregularities on the atomic scale,38, 39 which does not only favor protein adsorption,40 osteoblast differentiation,41 and expression of osteogenic markers42 but also causes high levels of adhesion upon contact, promoting facile formation and retention of stable aggregates even under relatively intensive agitations in the solution. This propensity of the particles to form aggregates subsequently stable in solution was used as the primary mechanism for loading the powders with small organic molecules.…”
Section: Resultsmentioning
confidence: 99%
“…For instance, fillers with high amounts of active surface hydrogen ions, generate strong filler-filler networks that can lead to agglomeration problems during processing and limit the reinforcement efficiency of the filler in most non-polar elastomers. Although high energy sites are mainly associated with functional groups [18,40,65], the surface activity also depends on the accessibility of these sites, which is determined by the arrangement and orientation of surface chemical groups [66,67]. Furthermore, high energy sites also can arise at structural heterogeneities, such as boundaries between crystallites and amorphous regions [19,67,68].…”
Section: Surface Activitymentioning
confidence: 99%
“…92,93 Together, these substitutions heavily influence the resulting chemistry of bone mineral in terms crystallinity, thermodynamic stability, morphology, solubility and biological properties. [94][95][96][97] Typically, HA exhibits two crystallographic forms; a hexagonal form that crystallises above 250 1C (P6 3 /m space group with unit cell parameters a = b = 9.432 Å, c = 6.881 Å) and a monoclinic form that crystallises below 250 1C (P2 1 /b space group with unit cell parameters a = 9.421 Å, b = 2 Å, c = 6.881 Å, b = 1201). 98,99 Whilst impurities can cause the Ca : P ratio of biological mineral to fall as low as 1.3, the combination of foreign ion inclusions, ionic vacancies and Ca 2+ deficiencies in fact contributes to stabilising biological HA in the hexagonal crystal form.…”
Section: àmentioning
confidence: 99%