Amorphous calcium phosphate

Biogenic ACP has been found in the inner ear of embryonic sharks, mammalian milk and dental enamel. However, whilst its unequivocal presence in bones and teeth is debated, there is evidence that transient amorphous precursors are involved in the development of bone and teeth.[4] The ACP in bovine milk (CPP-ACP) is believed to involve calcium phosphate nanoclusters in a shell of casein phosphopeptides. A typical casein micelle of radius 100 nm contains around 10,000 casein molecules and 800 nanoclusters of ACP, each about 4.8 nm in diameter. The concentration of calcium phosphate is higher in milk than in serum, but it rarely forms deposits of insoluble phosphates.[7] Unfolded phosphopeptides are believed to sequester ACP nanoclusters[8] and form stable complexes in other biofluids such as urine and blood serum, preventing deposition of insoluble calcium phosphates and calcification of soft tissue. In the laboratory, stored samples of formulations of artificial blood, serum, urine and milk (which approximate the pH of the naturally occurring fluid) deposit insoluble phosphates. The addition of suitable phosphopeptides prevents precipitation.[7]

Following investigations into the composition of amorphous calcium phosphates precipitated under different conditions, Posner and Betts suggested in the mid-1970s that the structural unit of ACP was a neutral cluster Ca₉(PO₄)₆.[4] Calculations support the description of a cluster with central Ca²⁺ ion surrounded by six phosphate PO₄³⁻ anions, which in turn are surrounded by eight further calcium ions.[9] The resulting cluster is estimated to have a diameter of around 950 pm (0.95 nm). These are now generally referred to as Posner's clusters. Precipitated ACP is believed to be made up of particles containing a number of Posner's clusters with water in the intervening spaces. While plasma spray coated ACP may contain Posner's clusters, there cannot be any water present.[4] New studies propose the idea of posner clusters acting as neural qbits because their entangled ³¹P have a long relaxation time and are in a S₆ symmetry. The idea behind it is that the posner molecules meld and release calcium-ions which stimulises the neurons.[10]

Amorphous calcium phosphate in combination with casein phosphopeptide has been used as a dental treatment to treat incipient dental decay. ACP sees its main use as an occluding agent, which aids in reducing sensitivity. Studies have shown that it does form a remineralized phase of hydroxyapatite consistent with the natural enamel. In addition, clinical studies have shown that patients who whiten their teeth have reduced sensitivity after treatment.[11] It is believed that ACP hydrolyzes under physiological temperatures and pH to form octacalcium phosphate as an intermediate, and then surface apatite.

ACP lacks the long-range, periodic atomic-scale order of crystalline calcium phosphates. The X-ray diffraction pattern is broad and diffuse with a maximum at ${\displaystyle 2\theta =25^{\circ }}$, and no other different features compared with well-crystallized hydroxyapatite. Under electron microscopy, its morphological form is shown as small spheroidal particles in the scale of tenths nanometer. In aqueous media, ACP is easily transformed into crystalline phases such as octacalcium phosphate and apatite due to the growing of microcrystallites. It has been demonstrated that ACP has better osteoconductivity and biodegradability than tricalcium phosphate and hydroxyapatite in vivo.[12]

Moreover, it can increase alkaline phosphatase activities of mesoblasts, enhance cell proliferation and promote cell adhesion. The unique role of ACP during the formation of mineralized tissues makes it a promising candidate material for tissue repair and regeneration. ACP may also be a potential remineralizing agent in dental applications. Recently developed ACP-filled bioactive composites are believed to be effective anti-demineralizing/remineralizing agents for the preservation and repair of tooth structures.[12]

• Remineralisation of teeth

• Mahamid, J.; Aichmayer, B.; Shimoni, E.; Ziblat, R.; Li, C.; Siegel, S.; Paris, O.; Fratzl, P.; Weiner, S.; Addadi, L. (2010). "Mapping amorphous calcium phosphate transformation into crystalline mineral from the cell to the bone in zebrafish fin rays". Proc. Natl. Acad. Sci. U.S.A. 107 (14): 6316–21. Bibcode:2010PNAS..107.6316M. doi:10.1073/pnas.0914218107. PMC 2851957. PMID 20308589.
• Zhao, J.; Liu, Y.; Sun, W. B.; Zhang, H. (2011). "Amorphous calcium phosphate and its application in dentistry". Chem. Cent. J. 5: 40. doi:10.1186/1752-153X-5-40. PMC 3143077. PMID 21740535.
• Ming S. Tung. "ACP Technology. Amorphous Calcium Phosphate forming Fluoride Varnishes" (PDF). American Dental Association. Archived from the original (PDF) on 2013-01-25.