Hydroxyapatite and

Both monocalcium phosphate and dicalcium phosphate dissolve incongmently in water, disproportionating to more basic calcium phosphate and phosphoric acid. The extent of these reactions varies with the temperature and the amount of water. If water is added gradually to anhydrous monocalcium phosphate, equiUbrium conditions first correspond to a mixture of the anhydrous salt and its monohydrate. After conversion to the monohydrate, further reaction affords dicalcium phosphate plus free phosphoric acid. Dicalcium phosphate decomposes in aqueous solution to the more basic hydroxyapatite and phosphoric acid via intermediate octacalcium phosphate. The compHcated stepwise conversion of the acidic mono- and dicalcium phosphates to hydroxyapatite is summarized in equations 6—9. The kinetics are quite complex. 

Dicalcium Phosphate Dihydrate (DPD). Dicalcium phosphate cHhydrate is completely nonreactive at room temperature. At 65—71°C and in the presence of water, it dehydrates and decomposes into hydroxyapatite and acidic monocalcium phosphate, or a free phosphoric acid (18). It is used to some extent in cake mixes in combination with faster acting acid. Its primary function is to provide acidity late in the baking cycle and thus produce a neutral and palatable product. DPD has an NV of 33. It provides sufficient acidity only in products requiring long baking times. 

In this work, simple (single-use) biosensors with a layer double stranded (ds) calf thymus DNA attached to the surface of screen-printed carbon electrode assembly have been prepared. The sensor efficiency was significantly improved using nanostructured films like carbon nanotubes, hydroxyapatite and montmorillonite in the polyvinylalcohol matrix. 

Similarly, a composite of hydroxyapatite and a network formed via cross-linking of chitosan and gelatin with glutaraldehyde was developed by Yin et al. [ 169]. A porous material, with similar organic-inorganic constituents to that of natural bone, was made by the sol-gel method. The presence of hydroxyapatite did not retard the formation of the chitosan-gelatin network. On the other hand, the polymer matrix had hardly any influence on the high crystallinity of hydroxyapatite. 

Sodium carboxymethyl chitin and phosphoryl chitin had most evident influences on the crystallization of calcium phosphate from supersaturated solutions. They potently inhibited the growth of hydroxyapatite and retarded the rate of spontaneous calcium phosphate precipitation. These chitin derivatives were incorporated into the precipitate and influenced both the phase and morphology of the calcium phosphate formed (flaky precipitate resembling octacalcium phosphate instead of spherical clusters in the absence of polysaccharide) [175]. 

T., Katutani, Y., and Kitsugi, T., Release of antibiotics from composites of hydroxyapatite and poly(lactic acid), in Advances in Drug Delivery Systems (J. M. Anderson and S. W. Kim, eds.), Elsevier, New York, 1986, pp. 179-186. 

Osteoclasts are multinucleated cells derived from pluripotent hematopoietic stem cells. Osteoclasts possess an apical membrane domain, exhibiting a ruffled border that plays a key role in bone resorption (Figure 48-12). A proton-translocating ATPase expels protons across the ruffled border into the resorption area, which is the microenvironment of low pH shown in the figure. This lowers the local pH to 4.0 or less, thus increasing the solubility of hydroxyapatite and allowing demineralization to occur. Lysosomal acid proteases are released that digest the now accessible matrix proteins. 

Aluminium ions released from the dental silicate cement are also absorbed by hydroxyapatite and have a similar beneficial effect to that of fluoride (Halse Hals, 1976 Putt Kleber, 1985). Thus, the dental silicate cement confers protection against caries (dental decay) on surrounding tooth material. 

Human body fluid and SBF contain calcium and phosphate ions that are already supersaturated with respect to hydroxyapatite [20]. However, these fluids do not spontaneously deposit hydroxyapatite under normal conditions. This is because the activation energy barrier for hydroxyapatite nudeation is very high. Therefore, the ability of substrates to induce heterogeneous nudeation of hydroxyapatite and the degree of supersaturation of SBF with respect to hydroxyapatite are important factors for hydroxyapatite formation on materials in the body fluid and SBF. 

Nano-hybrid Consisting of Bone-like Hydroxyapatite and Polymer... 

Fig. 11.17 XRD patterns of bone hydroxyapatite and sintered stoichiometric hydroxyapatite. (Bone hydroxyapatite was obtained by heating bone of pig at 600°C).

The secret to our success with hydroxyapatite and other strong calcium phosphates is that we seek syntheses for these bioceramics at temperatures on the order of400-800°C, where if hydroxyapatite is used as a reactant it does not decompose. Previously, most attempts failed to produce calcium phosphate bioceramic materials that were even 20% as strong as crystalline hydroxyapatite. Most crumbled under even moderate crompession in vivo. 

Hydroxyapatite and fluoroapatite surfaces differ from oxide surfaces in as far as they are expected to carry two different classes of surface groups (Wu et al., 1991). From a simple pictorial presentation... 

On the other hand, Wier et al (59) have shown that fluoride ions react with the surface of hydroxyapatite particles so that a state of equilibrium is reached as if the aqueous solution is in equilibrium with pure fluorapatite, provided that enough fluoride ions occur in the aqueous solution. Therefore, one should expect, that particles of solid solutions of hydroxyapatite and fluorapatite will react similarly with fluoride ions from an aqueous solution, and that a surface layer is formed which has a composition closer to that of pure fluorapatite than that of the original solid solution. 

In that study 5 ), the average of the logarithms of the solubility products for pure hydroxyapatite (log Kg / ) and pure fluorapatite (log Kp/ ) appeared to be - 59.16 and - 60.52 respectively, both with an uncertainty of about + 0.30. In the present study the solubility data found for equilibration of solid solutions are expressed as the negative logarithms for the ionic products of hydroxyapatite and fluorapatite, i.e. 

In conclusion, the solubility data indicate that upon precipitation from aqueous solutions which have a F/OH molar ratio less than a certain value, slightly fluoridated hydroxyapatites will be formed (x .0.15), and above that ratio nearly pure fluor-apatite will be formed. Usually the F/OH ratio varies so that intimate mixtures of hydroxyapatite and fluorapatite will result (64). The effect of fluoride on teeth and bones are discussed elsewhere (52, 57). 

Hydroxyapatite and titania are also useful stationary phase materials for biological samples. Hydroxyapatite, Cai0(PO4)6(OH)2, as a hexagonal column... 

Hyvonen PM, Kowolik MJ. Human neutrophil priming chemiluminescence modified by hydroxyapatite and three bisphosphonates in vitro. J Clin Lab Immunol 1993 40 69-76. 

Phosphate is remineralized during the oxidation of organic matter and dissolution of hard parts, such as bones and teeth, that are composed of the minerals hydroxyapatite and fluoroapatite. Unlike the other products of remineralization, pore-water phosphate concentrations are regulated only by mineral solubility, such as through vivianite (iron phosphate) and francolite (carbonate fluoroapatite). Redox reactions are not significant because phosphorus exists nearly entirely in the h-5 oxidation state. 

The nanostructured surfaces resemble, at least to a certain degree, the architecture of physiological adhesion substrates, such as extracellular matrix, which is composed from nanoscale proteins, and in the case of bone, also hydroxyapatite and other inorganic nanocrystals [16,17,24-27]. From this point of view, carbon nanoparticles, such as fullerenes, nanotubes and nanodiamonds, may serve as important novel building blocks for creating artificial bioinspired nanostructured surfaces for bone tissue engineering. 

Only a few systematic studies have been carried out on the mechanism of interaction of organic surfactants and macromolecules. Mishra et al. (12) studied the effect of sulfonates (dodecyl), carboxylic acids (oleic and tridecanoic), and amines (dodecyl and dodecyltrimethyl) on the electrophoretic mobility of hydroxyapatite. Vogel et al. (13) studied the release of phosphate and calcium ions during the adsorption of benzene polycarboxylic acids onto apatite. Jurlaanse et al.(14) also observed a similar release of calcium and phosphate ions during the adsorption of polypeptides on dental enamel. Adsorption of polyphosphonate on hydroxyapatite and the associated release of phosphate ions was investigated by Rawls et al. (15). They found that phosphate ions were released into solution in amounts exceeding the quantity of phosphonate adsorbed. 

Cholecalciferol (D3) and its active form 1,25-di-hydroxycholecalciferol are only to a certain extend vitamins because they can be synthesized by the human body. However deficiencies resulting in rickets in children and osteomalacia in adults do exist. Cholecalciferol can be synthesized by humans in the skin upon exposure to ultraviolet-B (UVB) radiation from sunlight, or it can be obtained from the diet. Plants synthesize ergosterol, which is converted to vitamin D2 (ergocalciferol) by ultraviolet light. Vitamin D2 may be less active in humans. Vitamin D promotes uptake of calcium and phosphate in the intestine and it stimulates osteoclasts to break down hydroxyapatite and release calcium into blood. Vitamin D is discussed in more detail in Chapter 24, Section V.a. 

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