Precursor Of Apatite Research Articles

Physicochemical and cytological properties of silicon-doping octacalcium phosphate

• Si was successfully doped in the metastable OCP crystals by a precipitation method. • Si doping led to the contraction of OCP structure with smaller lattice parameters. • Si doping preferred forming a cluster-like hierarchical structure of OCP crystals. • Si-OCP notably promoted the proliferation and osteogenic differentiation of BMSCs. • Si-OCPs enhanced the responses of BMSCs by ionic release and mineral deposits. Silicon was successfully doped into an intermediate precursor of biological apatite, octacalcium phosphate (OCP), accompanied with a lattice contraction. Si-doped OCP significantly enhanced the proliferation and osteogenic capacities of bone marrow mesenchymal stem cells by the synergistical effect of bioactive ions release and mineral deposits, providing a potential bone substitute.

Evaluation of quaternization effect on chitosan-HAP composite for bone tissue engineering application

This study attempts to improve the aqueous solubility of chitosan and utilizes it in the fabrication of composites with hydroxyapatite (HAP). The composites were evaluated as a curcumin delivery vehicle for bone regeneration. The chitosan was modified by quaternization, with a quaternization degree of 5 % for low quaternized chitosan (LQC) and 11 % for high quaternized chitosan (HQC). The modified chitosan, at alkaline pH 11, facilitated in situ HAP growth and formed LQC-HAP and HQC-HAP composites. The quaternization weakens intermolecular hydrogen bonds, facilitates interaction with the apatite precursor ions and promotes the growth of HAP. The modification significantly improved drug encapsulation (2.6 fold) but at the cost of a slight decrease in mechanical strength and increase in drug release. The in vitro studies with human osteoblast-like MG-63 cells established that the curcumin-loaded composites, LQC-HAP-C and HQC-HAP-C are biocompatible, encourage proliferation and promote a 2-fold increase in calcium mineralization over drug-free composites. The study exemplifies the reciprocity between quaternization degree and drug load/release properties and also illustrates that the magnitude of the latter reflects bioactivity. Thus, the quaternized chitosan-based HAP composite with tailorable bio-physicochemical properties becomes an interesting drug delivery system in bone regeneration.

Mineralogical-geochemical study of the anionic competition effect on the octacalcium phosphate reaction into fluorapatite

The unstable compound octacalcium phosphate (OCP) is one of the crystalline precursors of the apatite mineral series composed by hydroxyapatite, fluorapatite and chlorapatite. The feature of OCP to react into apatite, depending on the media conditions, has been mainly exploited for biomedical applications as bone and tooth substitute material. Recently, some important applications of OCP have been documented: e.g. as electrode material for supercapacitors and as fluoride remover reagent for environmental purposes. With the aim of deepening the property of OCP to be the crystalline precursor of apatite and assessing if and how the anionic competition can influence the formation of the different apatite end-members, the OCP → apatite reaction has been here investigated placing 0.223 mmol of OCP in 50 mL aqueous solution with 0.368 mmol of dissolved fluoride, chloride, hydroxyl and carbonate anions (fluoride alone, fluoride with each of the other anions, and all the anions together) at room temperature. The post-experiment analyses of solid and liquid phases, conducted by using XRD, ESEM and ICP-OES, show that fluoride is always the main anion removed from solution during the OCP transformation reaction. The precise mineralogical characterization of solid phases formed, performed using the Rietveld algorithm, shows that fluorapatite is always the main resulting apatitic phase, followed by hydroxyapatite. Taking into account the different application fields of OCP, these results could be significant in better defining the OCP → apatite reaction in aqueous solutions where different competing anions are involved.

A thermostability perspective on enhancing physicochemical and cytological characteristics of octacalcium phosphate by doping iron and strontium

Investigation of thermostability will lead the groundbreaking of unraveling the mechanism of influence of ion-doping on the properties of calcium phosphates. In this work, octacalcium phosphate (OCP), a metastable precursor of biological apatite, was used as a stability model for doping ions (Fe3+ and Sr2+) with different ionic charges and radii. After treated under hot air at different temperatures (110–200 °C), the phase, morphology, structure, physicochemical properties, protein affinity, ions release, and cytological responses of the ion-doped OCPs were investigated comparatively. The results showed that the collapse of OCP crystals gradually occurred, accompanying with the dehydration of hydrated layers and the disintegration of plate-like crystals as the temperature increased. The collapsed crystals still retained the typical properties of OCP and the potential of conversion into hydroxyapatite. Compared to the undoped OCP, Fe-OCP, and Sr-OCP had lower and higher thermostability respectively, leading to different material surface properties and ions release. The adjusted thermostability of Fe-OCP and Sr-OCP significantly enhanced the adsorption of proteins (BSA and LSZ) and the cytological behavior (adhesion, spreading, proliferation, and osteogenic differentiation) of bone marrow mesenchymal stem cells to a varying extent under the synergistic effects of corresponding surface characteristics and early active ions release. This work paves the way for understanding the modification mechanism of calcium phosphates utilizing ion doping strategy and developing bioactive OCP-based materials for tissue repair.

A Comprehensive Microstructural and Compositional Characterization of Allogenic and Xenogenic Bone: Application to Bone Grafts and Nanostructured Biomimetic Coatings

Bone grafts and bone-based materials are widely used in orthopedic surgery. However, the selection of the bone type to be used is more focused on the biological properties of bone sources than physico-chemical ones. Moreover, although biogenic sources are increasingly used for deposition of biomimetic nanostructured coatings, the influence of specific precursors used on coating’s morphology and composition has not yet been explored. Therefore, in order to fill this gap, we provided a detailed characterization of the properties of the mineral phase of the most used bone sources for allografts, xenografts and coating deposition protocols, not currently available. To this aim, several bone apatite precursors are compared in terms of composition and morphology. Significant differences are assessed for the magnesium content between female and male human donors, and in terms of Ca/P ratio, magnesium content and carbonate substitution between human bone and different animal bone sources. Prospectively, based on these data, bone from different sources can be used to obtain bone grafts having slightly different properties, depending on the clinical need. Likewise, the suitability of coating-based biomimetic films for specific clinical musculoskeletal application may depend on the type of apatite precursor used, being differently able to tune surface morphology and nanostructuration, as shown in the proof of concepts of thin film manufacturing here presented.

The influence of immersion in buffer systems simulating body fluids on properties and morphology of octacalcium phosphate granules

Octacalcium phosphate is the precursor of biological apatite, that is why it is of special interest in bone regeneration due to it’s biocompatibility and biodegradability. This study was performed to examine the in vitro stability of octacalcium phosphate granules in physiological solutions. Powder X-ray diffraction (XRD), infrared spectroscopy (IR), plasma atomic emission spectroscopy (AES) and scanning electron microscopy (SEM) data were obtained before and after granules immersion. The variation of Ca2+ and HPO42- concentration in the soaking solutions suggests that the material transformation occurs through octacalcium phosphate dissolution followed by hydroxyapatite precipitation.

Synthesis and in vitro biodegradation of pure octacalcium phosphate spheres

AbstractOctacalcium phosphate (OCP) is a key precursor of biological apatite in hard tissues with excellent osteoconductive and biodegradable properties for bone regeneration. OCP spherical granules are expected to be useful as drug delivery carriers, since OCP has high specific surface area. Although there have been some reports of OCP sphere preparation, methods for preparing pure OCP spheres are limited. The objective of this study is the preparation of spherical granules of pure OCP and assessment of their in vitro biodegradation in physiological conditions. We successfully prepared spherical pure OCP granules with a size of ~500 µm without any organic additives by simple immersion of α‐tricalcium phosphate spherical granules in pH 5.0 acetate buffered solutions at 60°C. The granules had core‐shell structure composed of OCP crystals different particle size. The spherical granules showed 20%‐40% in vitro degradation in physiological conditions; however, the phase transition of OCP was not significantly observed.

Comparison of microwave and conventionally sintered manganese and niobium doped lanthanum germanate based apatites by micro Raman Spectroscopy

In this paper, the effect of microwave and conventional sintering on doping behaviour of Mn2+ and Nb5+ in lanthanum germanate based apatite have been compared. The precursor of apatite has been prepared by mixed oxide method and conventionally calcined at 1100 °C for 6 h. The resulting powders have been sintered by microwave energy at 1400 °C for 30 min and by conventional heating 1400 °C for 4 h. The products prepared have been characterized by X-ray diffraction, scanning electron microscope, Micro Raman spectroscopy, and Vicker's hardness and the results are compared. The apatites of similar compositions sintered by microwave energy have higher density and hardness than the apatites sintered by electric heating.

In vivo and in vitro bioactivity of a “precursor of apatite” treatment on polyetheretherketone

We recently developed a surface treatment, “precursor of apatite” (PrA), for polyetheretherketone (PrA-PEEK) via a simple, low-temperature process aiming to achieve stronger and faster adhesion to bone. The treatment involves three steps: H2SO4 immersion, exposure to O2 plasma discharge, and alkaline simulated body fluid (alkaline SBF) treatment. This method produces homogeneous fine particles of amorphous calcium phosphate on the PEEK, and we confirmed that PrA-PEEK had excellent apatite formation ability in an SBF immersion test. In the present study using PEEK implants in rabbit tibia, mechanical tests, and histological and radiological analyses revealed that PrA provided the PEEK substrate with excellent bone-bonding properties and osteo-conductivity at early stages (4 and 8 weeks), extending to 16 weeks. In vitro study using MC3T3-E1 cells revealed via XTT assay that PrA on the PEEK substrate resulted in no cytotoxicity, though PrA treatment seemed to suppress gene expression of integrin β-1 and Alp after 7-day incubation as shown by real-time PCR. On the whole, PrA treatment succeeded in giving in vivo bone-bonding properties to the PEEK substrate, and the treatment is a safe and promising method that can be applied in clinical settings. There was an inconsistency between in vivo and in vitro bioactivity, and this discrepancy indicated that apatite formation does not always need activation of osteoblasts at very early stage and that optimal conditions at cell and organism level may be different. Statement of SignificancePolyetheretherketone (PEEK) is an attractive engineering polymer used for spine and dental surgery. To further improve clinical outcome of PEEK-based materials, we developed “Precursor of apatite” (PrA) treatment on the PEEK surface to confer bone-bonding properties. The advantages of this treatment are that it does not require high-temperature processing or special chemicals, and it is inexpensive. The present study clarified excellent in vivo bone-bonding property of PrA treatment. In addition, the results revealed important insights indicating that optimal conditions, especially wettability and crystallinity in calcium phosphate, differ at cell and organism levels. Moreover, our results indicated that prediction of in vivo bioactivity should be done in combination with multiple in vitro tests.

Dissolved fluoride removal by OCP, a precursor of apatite

The consumption of water with fluoride concentration higher than 1.5 mg/L (WHO recommended limit) is recognized to cause serious diseases. Fluoride removal from natural contaminated waters is a worldwide priority for more than 200 million people. The octacalcium phosphate (OCP), a mineralogical precursor of bio-apatite, is here tested as a fluoride remover. A new two-step method for the synthesis of OCP is proposed; it consists of 1) synthesis of brushite from calcium carbonate and phosphoric acid and, 2) subsequent hydrolysis of brushite. Fluoride removal experiments were performed in batch-mode using 200 mg of OCP in 50 ml solutions with different initial concentrations of fluoride (from 40 to 140 mg/L). Most of fluoride is removed within the first two hours, whereas the WHO limit of 1.5 mg/L is reached within a minimum of 3 hours for a starting Fconcentration of 40 mg/L, and in about 12 hours for a starting F-concentration of 80 mg/L. One gram of OCP can remove up to 26 mg of fluoride. The pH of the solution after the treatment is within the range of drinking water. XRD characterization of the solid phases, before and after the experiments, indicates that OCP transforms into fluorapatite via Fremoval from solution.

Authigenesis of biomorphic apatite particles from Benguela upwelling zone sediments off Namibia: The role of organic matter in sedimentary apatite nucleation and growth.

Sedimentary phosphorites comprise a major phosphorus (P) ore, yet their formation remains poorly understood. Extant polyphosphate-metabolizing bacterial communities are known to act as bacterial phosphate-pumps, leading to episodically high dissolved phosphate concentrations in pore waters of organic-rich sediment. These conditions can promote the precipitation of amorphous precursor phases that are quickly converted to apatite-usually in carbonate fluorapatite form [Ca10 (PO4 ,CO3 )6 F2-3 ]. To assess the mechanisms underpinning the nucleation and growth of sedimentary apatite, we sampled P-rich sediments from the Namibian shelf, a modern environment where phosphogenesis presently occurs. The P-rich fraction of the topmost centimetres of sediment mainly consists of pellets about 50-400μm in size, which in turn are comprised of micron-sized apatite particles that are often arranged into radial structures with diameters ranging from 2 to 4μm, and morphologies that range from rod-shapes to dumbbells to spheres that resemble laboratory-grown fluorapatite-gelatin nanocomposites known from double-diffusion experiments in organic matrices. The nucleation and growth of authigenic apatite on the Namibian shelf is likely analogous to these laboratory-produced precipitates, where organic macromolecules play a central role in apatite nucleation and growth. The high density of apatite nucleation sites within the pellets (>109 particles per cm3 ) suggests precipitation at high pore water phosphate concentrations that have been reported from the Namibian shelf and may be attributed to microbial phosphate pumping. The intimate association of organic material with the apatite could suggest a possible role of biological substrata, such as exopolymeric substances (EPS), in the nucleation of apatite precursors. Importantly, we do not observe any evidence that the apatite particles are actual phosphatized microbes, contradicting some earlier studies. Nevertheless, these results further evidence the potential importance of microbially derived (extracellular) organic matter as a template for phosphatic mineral nucleation in both recent and ancient phosphorites.

The trace element and U-Pb systematics of metamorphic apatite

Abstract Apatite is a common accessory mineral in igneous, sedimentary and metamorphic rocks. It has potential as a provenance indicator in sedimentary systems, as it can host a wide variety of trace elements in its crystal structure and can yield thermochronological age information. However, the processes controlling the trace element and U-Pb systematics of metamorphic apatite remain poorly understood, and metamorphic apatite remains significantly under-represented in compositional provenance databases linking apatite trace-element chemistry to its corresponding parent rock type. We investigate the trace-element and U-Pb systematics of metamorphic apatite from a suite of 22 bedrock samples of diverse metamorphic grade and protolith type, sampled from a variety of metamorphic terranes. Metamorphic apatite from low- to medium-grade metapelites and metabasites can be easily distinguished from granitic apatite as it is significantly depleted in Th, REE, and Y. Depletion in Th and REE + Y is attributed to growth of co-genetic epidote, which is the dominant carrier phase of the REE + Y, Th, and U in all the low- to medium-grade samples mapped by laser ablation quadrupole inductively coupled plasma mass spectrometry (LA-Q-ICP-MS) and energy dispersive X-ray spectroscopy (EDS). Apatite U contents in low- to medium-grade metapelites and metabasites are more variable than the Th and REE + Y contents, but are typically low. Consequently, grains from these rock types are often undateable by the U-Pb LA-ICP-MS method and thus are underrepresented in apatite U-Pb detrital datasets, but can still be identified as low- to medium-grade metamorphic apatite by their trace-element characteristics. Low-grade metapelite apatite is difficult to distinguish from low-grade metabasite apatite, which is likely due to the growth of U-, Th-, and REE-rich epidote in both lithologies. Detrital (granitic) apatite is stable in very low-grade (e.g. pumpellyite-actinolite facies) metasedimentary samples, while neo- or re-crystallized metamorphic apatite is widespread by the upper-greenschist facies. LA-Q-ICP-MS imaging demonstrates that low REE + Y, Th, and U metamorphic apatite rims can nucleate on detrital igneous apatite precursors with high REE + Y, Th, and U. With increasing metamorphic grade, 1) relict detrital apatite is consumed, 2) the coherence of the U-Pb concordia systematics dating metamorphism improves, and 3) the degree of dispersion on metamorphic apatite multi-element plots decreases. The highest-grade metamorphic apatite samples investigated are paragneisses, some of which have locally undergone anatexis. Apatites from these samples yield well constrained TW concordia intercept ages and minor dispersion on multi-element plots (which is attributed to the absence of epidote) and closely resemble apatite from S-type granites in their trace element characteristics.

Fabrication of Bioactive Fiber-reinforced PEEK and MXD6 by Incorporation of Precursor of Apatite.

We aimed to develop an effective process to provide bioactivity to carbon fiber-reinforced polyetheretherketone (PEEK), glass fiber-reinforced PEEK and glass fiber-reinforced poly(m-xylyleneadipamide)-6 (MXD6), possessing similar elastic modulus to cortical bone in this study. First, we formed fine pores on the surface of each substrate by a short-time sulfuric acid treatment. Second, in order to provide hydrophilic property, we treated the surfaces of each substrate with oxygen plasma. Finally, we deposited fine particles of amorphous calcium phosphate (PrAp) in the pores by soaking each substrate in SBF adjusted at pH 8.40, 25.0°C, and subsequently kept at 70.0°C for 24 h. By this treatment, we obtained the bioactive fiber-reinforced polymers. By soaking thus-obtained each material in SBF, apatite formation was induced on the whole surface of each substrate within 1 day by PrAp deposited in the pores and high apatite-forming ability was performed on each material. The adhesive strength between the apatite layer showed high value by mechanical anchoring effect generated by the apatite formed in the pores. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2254-2265, 2018.

Regulating the physicochemical and biological properties in vitro of octacalcium phosphate by substitution with strontium in a large doping range

Octacalcium phosphate (OCP) is a key precursor of biological apatite in bone and teeth with excellent osteoconductive and biodegradable properties for bone regeneration. In this work, strontium was employed for improving the poor bioactivity and osteogenesis of OCP by ionic substitution using a homogeneous precipitation method. Sr was successfully incorporated in the structure within a fairly large doping range, even up to 23.25 mol.%, leading to lattice expansion and preferred growth. Sr-OCP samples with better cellular affinity had significantly enhanced the viability, proliferation and osteogenic differentiation of bone mesenchymal stem cells, compared with control. Dynamically released biological ions were involved in the biological apatite deposition for biomineralization/cellular calcification, and remarkably promoted the osteogenic ability. Results indicated the effective enhancements of Sr substitution on the biocompatibility, bioactivity and osteogenesis of OCP biomaterials, providing a potential strategy for the accounts of ionic substitution in biomaterials and the following bone repair applications.

Effect of pores formation process and oxygen plasma treatment to hydroxyapatite formation on bioactive PEEK prepared by incorporation of precursor of apatite

When bioinert substrates with fine-sized pores are immersed in a simulated body fluid (SBF) and the pH value or the temperature is increased, fine particles of calcium phosphate, which the authors denoted as ‘precursor of apatite’ (PrA), are formed in the pores. By this method, hydroxyapatite formation ability can be provided to various kinds of bioinert materials. In this study, the authors studied fabrication methods of bioactive PEEK by using the above-mentioned process. First, the fine-sized pores were formed on the surface of the PEEK substrate by H2SO4 treatment. Next, to provide hydrophilic property to the PEEK, the surfaces of the PEEK were treated with O2 plasma. Finally, PrA were formed in the pores by the above-mentioned process, which is denoted as ‘Alkaline SBF’ treatment, and the bioactive PEEK was obtained. By immersing in SBF with the physiological condition, hydroxyapatite formation was induced on the whole surface of the substrate within 1day. The formation of PrA directly contributed to hydroxyapatite formation ability. By applying the O2 plasma treatment, hydroxyapatite formation was uniformly performed on the whole surface of the substrate. The H2SO4 treatment contributed to a considerable enhancement of adhesive strength of the formed hydroxyapatite layer formed in SBF because of the increase of surface areas of the substrate. As a comparative study, the sandblasting method was applied as the pores formation process instead of the H2SO4 treatment. Although hydroxyapatite formation was provided also in this case, however, the adhesion of the formed hydroxyapatite layer to the substrate was not sufficient even if the O2 plasma treatment was conducted. This result indicates that the fine-sized pores should be formed on the whole surface of the substrate uniformly to achieve high adhesive strength of the hydroxyapatite layer. Therefore, it is considered that the H2SO4 treatment before the O2 plasma and the ‘Alkaline SBF’ treatment is an important factor to achieve high adhesive strength of hydroxyapatite layer to the PEEK substrate. This material is expected to be a candidate for next-generation implant materials with high bioactivity.

The Bone Building Blues: Self-hardening copper-doped calcium phosphate cement and its in vitro assessment against mammalian cells and bacteria

A blue calcium phosphate cement with optimal self-hardening properties was synthesized by doping whitlockite (β-TCP) with copper ions. The mechanism and the kinetics of the cement solidification process were studied using energy dispersive X-ray diffraction and it was found out that hardening was accompanied by the phase transition from TCP to brushite. Reduced lattice parameters in all crystallographic directions resulting from the rather low (1:180) substitution rate of copper for calcium was consistent with the higher ionic radius of the latter. The lower cationic hydration resulting from the partial Ca→Cu substitution facilitated the release of constitutive hydroxyls and lowered the energy of formation of TCP from the apatite precursor at elevated temperatures. Addition of copper thus effectively inhibited the formation of apatite as the secondary phase. The copper-doped cement exhibited an antibacterial effect, though exclusively against Gram-negative bacteria, including E. coli, P. aeruginosa and S. enteritidis. This antibacterial effect was due to copper ions, as demonstrated by an almost negligible antibacterial effect of the pure, copper-free cement. Also, the antibacterial activity of the copper-containing cement was significantly higher than that of its precursor powder. Since there was no significant difference between the kinetics of the release of copper from the precursor TCP powder and from the final, brushite phase of the hardened cement, this has suggested that the antibacterial effect was not solely due to copper ions, but due to the synergy between cationic copper and a particular phase and aggregation state of calcium phosphate. Though inhibitory to bacteria, the copper-doped cement increased the viability of human glial E297 cells, murine osteoblastic K7M2 cells and especially human primary lung fibroblasts. That this effect was also due to copper ions was evidenced by the null effect on viability increase exhibited by the copper-free cements. The difference in the mechanism of protection of dehydratases in prokaryotes and eukaryotes was used as a rationale for explaining the hereby evidenced selectivity in biological response. It presents the basis for the consideration of copper as a dually effective ion when synergized with calcium phosphates: toxic for bacteria and beneficial for the healthy cells.

Reprint of “Biomimetic apatite coating on yttria-stabilized tetragonal zirconia utilizing femtosecond laser surface processing”

Yttria-stabilized tetragonal zirconia polycrystals (Y-TZP) have been used in orthopedic and dental implants because of their excellent physicochemical properties. In this study, we developed an apatite coating technique with low thermal effects for Y-TZP ceramics based on a biomimetic process using a supersaturated calcium phosphate solution (CP solution) as a coating medium. To achieve this, we performed femtosecond laser processing with low thermal effects as a surface pre-modification tool for Y-TZP ceramics. By changing the laser scanning mode, we fabricated two different submicro-/micro-structures on the Y-TZP sample. Both laser-treated samples showed increased water wettability due to ablation plasma and partly formed an apatite layer on their surfaces in the CP solution within 7 days. To further enhance the apatite-forming ability, we applied an alternate dipping process to the laser-treated sample in order to precoat the sample with apatite precursors. The laser-treated and precursor-precoated sample successfully formed an apatite layer on the entire surface in the CP solution within a shorter time period (24 h). The thus-coated apatite layer adhered to the sample so strongly that the layer remained on the sample even after the tape-detaching test. This strong adhesion may be attributed to the mechanical interlocking effects due to laser-induced surface roughening. Our proposed apatite-coating technique using the laser- and precursor-assisted biomimetic process would be useful for the creation of apatite-coated Y-TZP ceramics for orthopedic and dental applications.

Controlled and Tunable Biomimetic Apatite Mineralization of Synthetic Hydrogels

There has been much work examining bioinspired mineralization of polymeric hydrogels with calcium phosphates, yet a systematic method for the predictable and tunable synthesis of biomimetic apatites is yet to be developed. Here, a method for the selective mineralization of substituted apatite composite hydrogels where the incorporated mineral phase is formed as a result of a chemical reaction within the hydrogel matrix is presented. Mineralized hydrogels are prepared by precipitating the apatite precursor phase dicalcium phosphate dihydrate (DCPD) in a poly(vinyl alcohol) (PVA) solution, which is then crosslinked into a composite hydrogel by cyclic freeze/thawing. The encapsulated DCPD is hydrolyzed to apatite by immersion in buffers at 37 °C. Tuning the pH (7.4, 9) and ionic composition (CO3 2−, F−) of the buffer influence the morphology and chemical composition of the apatite product. The incorporated calcium phosphate polymorph is monitored by X‐ray diffraction, attenuated total reflectance‐fourier transform infrared spectroscopy (ATR‐FTIR), and scanning electron microscope‐energy dispersive X‐ray. The apatite–PVA hydrogels promote cellular adhesion and viability. The method developed here demonstrates diffusion‐mediated transformation of a calcium phosphate precursor phase within a hydrogel matrix to various substituted apatites in a selective and predictable manner.image

Biomimetic apatite coating on yttria-stabilized tetragonal zirconia utilizing femtosecond laser surface processing

Abstract Yttria-stabilized tetragonal zirconia polycrystals (Y-TZP) have been used in orthopedic and dental implants because of their excellent physicochemical properties. In this study, we developed an apatite coating technique with low thermal effects for Y-TZP ceramics based on a biomimetic process using a supersaturated calcium phosphate solution (CP solution) as a coating medium. To achieve this, we performed femtosecond laser processing with low thermal effects as a surface pre-modification tool for Y-TZP ceramics. By changing the laser scanning mode, we fabricated two different submicro-/micro-structures on the Y-TZP sample. Both laser-treated samples showed increased water wettability due to ablation plasma and partly formed an apatite layer on their surfaces in the CP solution within 7 days. To further enhance the apatite-forming ability, we applied an alternate dipping process to the laser-treated sample in order to precoat the sample with apatite precursors. The laser-treated and precursor-precoated sample successfully formed an apatite layer on the entire surface in the CP solution within a shorter time period (24 h). The thus-coated apatite layer adhered to the sample so strongly that the layer remained on the sample even after the tape-detaching test. This strong adhesion may be attributed to the mechanical interlocking effects due to laser-induced surface roughening. Our proposed apatite-coating technique using the laser- and precursor-assisted biomimetic process would be useful for the creation of apatite-coated Y-TZP ceramics for orthopedic and dental applications.

Apatite Biominerals

Calcium phosphate apatites offer outstanding biological adaptability that can be attributed to their specific physico-chemical and structural properties. The aim of this review is to summarize and discuss the specific characteristics of calcium phosphate apatite biominerals in vertebrate hard tissues (bone, dentine and enamel). Firstly, the structural, elemental and chemical compositions of apatite biominerals will be summarized, followed by the presentation of the actual conception of the fine structure of synthetic and biological apatites, which is essentially based on the existence of a hydrated layer at the surface of the nanocrystals. The conditions of the formation of these biominerals and the hypothesis of the existence of apatite precursors will be discussed. Then, we will examine the evolution of apatite biominerals, especially during bone and enamel aging and also focus on the adaptability of apatite biominerals to the biological function of their related hard tissues. Finally, the diagenetic evolution of apatite fossils will be analyzed.