PubMed Health⌕ Search

PubMed · 33203

Biological apatite crystal disolution.

Abstract

The dissolution curves of human acid-treated enamel powder are characterized by a rapid initial step followed, after 10 or 15 minutes, by a second stage, with release of very small amounts of calcium. Increase in pH and addition of fluoride ions tend to diminish, for short intervals, the amount of dissolved apatites. For higher pH values the decrease is noted over a longer time. Study of the relative ionic variation of human enamel powder from young and adult patients subjected to acid requires infra-red vibration band analyses. Special attention was given to the absorptions at 610 cm-1 (phosphate groups), 880 cm-1 (CO32- in OH- sites and HPO42-), 1410 cm-1 (CO32- in phosphate sites) and 1550 cm-1 (CO32- in OH- position). All results were related to vibration band at 610 cm-1. A preferential loss of carbonates in the two possible sites was always observed for 10 or 15 minutes, followed by a high release of phosphate. The increase of pH or small amounts of fluoride displaced the preferential carbonate loss to longer times. In the presence of higher fluoride levels a disappearance of the preferential loss of carbonates was noted. A continuous increase of HPO42- in the absence of fluoride occurred; however a straight line with a smaller shape was present, with fluoride addition.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J C Voegel, P Garnier. 1979. Biological apatite crystal disolution.. https://doi.org/10.1177/00220345790580023801

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Plasma-controlled nanocrystallinity and phase composition of TiO2: a smart way to enhance biomimetic response.

This contribution sheds light on the role of crystal size and phase composition in inducing biomimetic apatite growth on the surface of nanostructured titania films synthesized by reactive magnetron sputtering of Ti targets in Ar+O(2) plasmas. Unlike most existing techniques, this method enables one to deposit highly crystalline titania films with a wide range of phase composition and nanocrystal size, without any substrate heating or postannealing. Moreover, by using this dry plasma-based method one can avoid surface hydroxylation at the deposition stage, almost inevitable in wet chemical processes. Results of this work show that high phase purity and optimum crystal size appear to be the essential requirement for efficient apatite formation on magnetron plasma-fabricated bioactive titania coatings.

Apatites↗

CO2 laser-induced zonation in dental enamel: a Raman and IR microspectroscopic study.

The gradient of structural alteration and molecular exchange across CO(2) laser-irradiated areas in dental enamel was analyzed by Raman and attenuated total reflectance infrared microspectroscopy. The type and the degree of structural changes in morphologically distinguishable zones within the laser spot vary depending on the laser-irradiation parameters--power (1 and 3 W), treatment time (5 and 10 s), and operational mode (super pulse and continuous wave). Using higher power, irrespective of the operation mode, the enamel tissue ablates and a crater is formed. The prevalent phase at the bottom of the crater is dehydrated O(2) (2-)-bearing apatite, that is, the fundamental framework topology is preserved. Additional nonapatite calcium phosphate phases are located mainly at the slope of the laser crater. No structural transformation of mineral component was detected aside the crater rim, only a CO(3)-CO(2) exchange, which decays with the radial distance. A lower-power laser irradiation slightly roughens the enamel surface and the structural modification of enamel apatite is considerably weaker for continuous wave than for super pulse mode. Prolonged low-power laser treatment results in recrystallization, and thus structural recovering of apatite might be of clinical relevance for enamel surface treatments.

Apatites↗

The in vitro bioactivity of two novel hydrophilic, partially degradable bone cements.

Composite bone cements were prepared with bioactive glasses (MgO-SiO(2)-3CaO.P(2)O(5)) of different reactivities. The matrix of these so-called hydrophilic, partially degradable and bioactive cements was composed of a starch/cellulose acetate blend and poly(2-hydroxyethyl methacrylate). The addition of 30 wt.% of glasses to this system made them bioactive in acellular medium: a dense apatite layer formed on the surface after 7 days of immersion in simulated body fluid. This was demonstrated both by microscopic and infrared spectroscopic techniques. The composition of the glass and, consequently, its structure was found to have important effects on the rate of the apatite formation. The combination of reactivity obtained by one formulation with the hydrophilic and degradable character of these cements makes them a very promising alternative to conventional acrylic bone cements, by allowing a better stabilization of the implant and a stronger adhesion to the bone.

Apatites↗