PRECIPITATION OF HYBRID HYDROXYAPATITE / AUTOFIBRIN NANOCOMPOSITES

Синтезированы гибридные нанокомпозиты на основе гидроксиапатита и аутофибрина в форме фибринового сгустка либо цитратной плазмы путем осаждения при pH 9. «Мягкие» условия осаждения и быстрое выделение нанокомпозитов способствовали сохранению биополимерной матрицы аутофибрина. Дестабилизация дополнительной фазы аморфного фосфата кальция с образованием стехиометрического гидроксиапатита обусловлена влиянием макромолекул фибрина. Формирование кальцийдефицитного гидроксиапатита с x« 0,1 и Ca / P 1,65 происходило в среде цитратной плазмы, который после 800 °С превращался в смесь гидроксиапатит / 3 -трикальцийфосфат. Синтез композитов на основе биомиметического апатита осуществляли при добавлении 30 об.% модельного раствора Simulated Body Fluid (SBF). Влияние ионов Mg, CO~, входящих в состав SBF, способствовало стабилизации аморфного фосфата кальция и образованию карбонатзамещенного гидроксиапатита, устойчивого к термическим превращениям до 800°С. Совокупное влияние аутофибрина и ионов введенного SBF позволило управлять составом минеральной составляющей гибридных нанокомпозитов без разрушения биополимерной матрицы. Hybrid composites based on hydroxyapatite and autofibrin were synthesized by precipitation in a medium with pH = 9. Soft precipitation conditions and rapid isolation of the composite precipitates favored preservation of a biopolymer matrix of autofibrin. An effect of fibrin macromolecules contributed to destabilization of the amorphous calcium phosphate phase and formation of stoichiometric hydroxyapatite. The medium of the citrated plasma stimulated precipitation of calcium-deficient hydroxyapatite with x « 0,1 and the Ca / P ration of 1,65 which transformed into the mixture of hydroxyapatite / 3 -tricalcium phosphate at 800 °С. Biomimetic apatite composites were synthesized with an addition of 30 vol. % of a Simulated Body Fluid (SBF) model solution. The effect of Mg, CO~ ions of SBF promoted the stabilization of amorphous calcium phosphate and formation of carbonated hydroxyapatite that exhibited thermal stability up to 800 °С. The cummulative effect of autofibrin and ions of induced SBF provided controlling composition of the mineral part of hybrid nanocomposites without disruption of an autofibrin matrix.

In situ luminescence analysis: a new light on monitoring calcium phosphate phase transitions

In situ luminescence measurements allow monitoring the phase transitions of biologically relevant calcium phosphates with high sensitivity, independent of synchrotron radiation.

Sintering Behavior of Nanostructured Hydroxyapatite Ceramics

The synthesis of nanoparticles appropriate for the preparation of nanostructured hydroxyapatite ceramics intended for bone repairs and regeneration is an interesting field of biomaterials research today. In this work nanoparticles of hydroxyapatite were obtained by the precipitation method using conventional magnetic stirring (A) and ultra turrex homogenizer (T1) accompanied with surfactant (T2) and dispersant agents (T3). In all cases, powders with nanometric dimensions were obtained and the unique calcium phosphate phase detected was hydroxyapatite (HAp). The powders sintering behaviour was studied. The ceramics obtained from powders prepared by magnetic stirring (A) showed the best values of final density (96.7 %) which it was in agreement with the lowest temperature of the beginning of shrinking (648.6 °C) during sintering determined by dilatometry. Nanostructured nature of these ceramics was confirmed by Scanning Electron Microscopy (SEM).

Stabilizing amorphous calcium phosphate phase by citrate adsorption

Citrate controls nucleation by association with a precursor amorphous phase, which inhibits the surface reaction for nucleation.

Synchrotron X-Ray Microanalysis and Imaging of Synthetic Biological Calcium Carbonate in Comparison With Archaeological Samples Originating from the Large Cave of Arcy-sur-Cure (28000-24500 BP, Yonne, France)

Biosynthetic calcite samples were investigated using combined synchrotron X-ray microspectroscopy mapping. These samples were prepared with bacteria isolated from the Large cave of Arcy-sur-Cure in which prehistoric figures are masked by an opaque calcite layer. The biotic or abiotic origin of this layer is the issue of the present work. As previously known, a large community of bacteria may be involved in the CaCO3 formation in caves. A mixture of calcite/vaterite was obtained from bacteria isolated from the cave. Therefore, we can offer conclusions on their calcifying capability. The rare presence of vaterite in cave environments may be treated as a marker of biotic carbonate formations. Moreover, an amorphous calcium phosphate phase was present in the form of a calcite/vaterite mixture in the biotic model samples. This mixture of phases could be used as a tracer of the biotic process of CaCO3 formation. These biotic tracer phases were not identified using the applied analytical methods in the natural samples taken from the opaque calcite layers that covered the prehistoric figures of the Large cave. In this case, based on the obtained results, the biotic calcite formation process is likely to be considered as an undetectable effect at minimum.

Comparative Study on Bioresorbability of Chelate-Setting Cements with Various Calcium-Phosphate Phase Using Rabbit Model

We have developed novel calcium-phosphate cements (CPCs) based on the chelate-setting mechanism of inositol phosphate (IP6) using hydroxyapatite (HAp), β-tricalcium phosphate (β-TCP) and α-TCP as starting materials. These cements (IP6-HAp, IP6-β-TCP and IP6-α-TCP cements) have different bioresorbability due to the chemical composition of starting materials. In the present study, biocompatibility and bioresorbability of the above three cements and commercially available cement (Biopex®-R) was histologically evaluated in vivo using rabbit model for 4, 8, and 24 weeks, in addition to their dissolution in vitro. The dissolution of these cements increased in the order of IP6-HAp, IP6-β-TCP and IP6-α-TCP cements. The newly-formed bones were directly in contact with both the IP6-HAp and Biopex®-R cement specimens. As for the IP6-β-TCP and IP6-α-TCP cements, newly-formed bones were formed time-dependently slightly apart from the cement specimens. Resorption rate for Biopex®-R, IP6-HAp, IP6-β-TCP, and IP6-α-TCP cements after 24 weeks implantation were of 7.2, 5.0, 13.7, and 16.2%, respectively, compared to original cements. The present chelate-setting cements with different bioresorbability are promising candidates for application as the novel CPCs.