Fabrication of pure octacalcium phosphate blocks from dicalcium hydrogen phosphate dihydrate blocks via a dissolution–precipitation reaction in a basic solution

2019 ◽  
Vol 239 ◽  
pp. 143-146 ◽  
Author(s):  
Yuki Sugiura ◽  
Kunio Ishikawa
Materials ◽  
2017 ◽  
Vol 10 (4) ◽  
pp. 374 ◽  
Author(s):  
Kanji Tsuru ◽  
Ayami Yoshimoto ◽  
Masayuki Kanazawa ◽  
Yuki Sugiura ◽  
Yasuharu Nakashima ◽  
...  

Author(s):  
Shiv Prakash Mishra

The octacalcium phosphate (OCP) crystals are apatite bases with hydrated layers in producing of needle or plate-shaped hydroxyapatite (HAP) nanocrystals, which prepared by a dissolution precipitation reaction. The reaction led to a hexagonal HAP nanocrystals formation under hydrothermal condition via OCP at 180? for 3h with pH of solution adjusted to 5.5 with incorporating dicarboxylate or succinate ions having Ca/P molar ratio is expected to be 1.56±0.02, where the morphology of OCP are retained. During incorporating of succinate ions in OCP crystals, the hydrogen phosphate (HPO42-) ions in the hydrated layers of OCP are being substituted by succinate ions. These organically modified OCP which generated to HAP with unique nanostructures have been characterized by using of SEM, FTIR and X-ray diffraction analysis. Since the crystal system of HAP is hexagonally and its crystalline size in the direction of various (a,b,c) axes depending on the thickness of the plate-shaped HAP crystals where their size as perpendicular to the (100) plane is calculated by using of Scherrer equation D100 = K?/(? cos?). The formed hexagonal HAP are used in soft and hard tissue engineering system for biomedical application.


2021 ◽  
Vol 9 (10) ◽  
pp. 707-712
Author(s):  
Shiv Prakash Mishra ◽  

In chemistry of inorganic crystals, the octacalcium phosphate (OCP) is an apatite based crystals and having a hydrated layers which used in producing of needle or plate-shaped hydroxyapatite (HAP) nanocrystals. Although, the crystals is prepared by a dissolution precipitation reaction. These reaction led to a hexagonal HAP nanocrystals formation under hydrothermal condition from OCP at 180 for 3 hours with pH of solution adjusted to 5.5 and incorporating dicarboxylate e.g. succinate (OOC.(CH2)2.COO)2- ions having Ca/P molar ratio is expected to be 1.56±0.02, where the morphology of OCP are retained. During incorporating of succinate ions in OCP crystals, the hydrogen phosphate (HPO42-) ions in the hydrated layers of OCP are being substituted by succinate ions. Since the crystal system of HAP is hexagonal and its crystalline size in the longitudinal direction of various (a,b,c) axes depending on the thickness of the laminated plate-shaped HAP crystals. Here, their size as perpendicular to the (100) plane which is calculated by introducing of Scherrers equation, D100 = Kλ/(β cos ). The organically modified OCP which generated to HAP have unique nanostructure with micrometer thickness are characterized by using of SEM, FTIR and X-ray diffraction analysis.


2019 ◽  
Vol 10 (1) ◽  
pp. 11 ◽  
Author(s):  
Katia Rubini ◽  
Elisa Boanini ◽  
Adriana Bigi

Dicalcium phosphate dihydrate (DCPD) is one of the mineral phases indicated as possible precursors of biological apatites and it is widely employed in the preparation of calcium phosphate bone cements. Herein, we investigated the possibility to functionalize DCPD with aspartic acid (ASP) and poly-aspartic acid (PASP), as models of the acidic macromolecules of biomineralized tissues, and studied their influence on DCPD hydrolysis. To this aim, the synthesis of DCPD was performed in aqueous solution in the presence of increasing concentrations of PASP and ASP, whereas the hydrolysis reaction was carried out in physiological solution up to three days. The results indicate that it is possible to prepare DCPD functionalized with PASP up to a polyelectrolyte content of about 2.3 wt%. The increase of PASP content induces crystal aggregation, reduction of the yield of the reaction and of the thermal stability of the synthesized DCPD. Moreover, DCPD samples functionalized with PASP display a slower hydrolysis than pure DCPD. On the other hand, in the explored range of concentrations (up to 10 mM) ASP is not incorporated into DCPD and does not influence its crystallization nor its hydrolysis. At variance, when present in the hydrolysis solution, ASP, and even more PASP, delays the conversion into the more stable phases, octacalcium phosphate and/or hydroxyapatite. The greater influence of PASP on the synthesis and hydrolysis of DCPD can be ascribed to the cooperative action of the carboxylate groups and to its good fit with DCPD structure.


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