Effect Of Calcium Phosphate Research Articles

Effects of calcium phosphate and phosphorus-dissolving bacteria on microbial structure and function during Torreya Grandis branch waste composting

Background Burkholderiais a phosphorus solubilizing microorganism discovered in recent years, which can dissolve insoluble phosphorus compounds into soluble phosphorus. To investigate the effects of Burkholderia and calcium phosphate on the composting of Torreya grandis branches and leaves, as well as to explain the nutritional and metabolic markers related to the composting process.MethodsIn this study, we employed amplicon sequencing and untargeted metabolomics analysis to examine the interplay among phosphorus (P) components, microbial communities, and metabolites during T. grandis branch and leaf waste composting that underwent treatment with calcium phosphate and phosphate-solubilizing bacteria (Burkholderia). There were four composting treatments, 10% calcium phosphate (CaP) or 5 ml/kg (1 × 108/ml Burkholderia) microbial inoculum (WJP) or both (CaP + WJP), and the control group (CK).ResultsThe results indicated that Burkholderia inoculation and calcium phosphate treatment affected the phosphorus composition, pH, EC, and nitrogen content. Furthermore, these treatments significantly affected the diversity and structure of bacterial and fungal communities, altering microbial and metabolite interactions. The differential metabolites associated with lipids and organic acids and derivatives treated with calcium phosphate treatment are twice as high as those treated with Burkholderia in both 21d and 42d. The results suggest that calcium phosphate treatment alters the formation of some biological macromolecules.ConclusionBoth Burkholderia inoculation and calcium phosphate treatment affected the phosphorus composition, nitrogen content and metabolites of T. grandis branch and leaf waste compost.These results extend our comprehension of the coupling of matter transformation and community succession in composting with the addition of calcium phosphate and phosphate-solubilizing bacteria.

Inorganic Phosphate as "Bioenergetic Messenger" Triggers M2-Type Macrophage Polarization.

The effects of calcium phosphate (CaP) materials on macrophage polarization state vary with their physicochemical properties. The study aims to elucidate the impact of phosphate ion-mediated energy metabolism on M2 macrophage polarization and the corresponding regulatory mechanism. The phosphate ions released from CaP ceramic as bioenergetic factor is identified; its concentration is closely associated with the polarized state. After being taken up by the sodium-dependent phosphate transporter 1, extracellular phosphate ions produce energy via oxidative phosphorylation by facilitating tricarboxylic acid flux, thereby contributing to M2 macrophage polarization. Further mechanistic analysis reveals that the elevation of the bioenergetic basis can drive macrophage M2 polarization via the AMP-activated protein kinase-mammalian target of rapamycin (AMPK-mTOR) axis. Another regulatory effect is that of the adenosine triphosphate (ATP), a signaling molecule. Intracellular ATP is released into the extracellular space and degraded to adenosine, which serves as a signaling molecule through the A2b adenosine receptor to activate the cyclic adenosine monophosphate (cAMP) pathway, thereby promoting M2 macrophage polarization. Overall, these findings may transform the existing knowledge on cell metabolism and energy homeostasis from bystanders to pivotal factors guiding M2 macrophage polarization and have implications for the future design of biomimetic CaP scaffolds.

The Effect of Dentin Treated with Calcium Phosphate Desensitizer on Shear Bond Strength with Different Resin Cement: An In Vitro Study

Aim: The aim of this study was to evaluate the effect of calcium phosphate based desensitizing agent on shear bond strength of self-etch/adhesive resin cements to dentin. Materials and Methods: Eighty dentin specimens were prepared from freshly extracted human third molar teeth and were classified, randomly ( n = 20). Half of groups were treated with calcium phosphate based Teethmate Desensitizer and then Panavia V5, RelyX Ultimate (containing self-etch primer), Panavia SA, and RelyX U200 self-adhesive resin cements were luted to all dentin surfaces. All specimens were stored in an incubator at 37°C for 24 h. Shear bond strength was tested by a universal test machine at a 0.5 mm/min crosshead speed. The data were analyzed with a statistical program. Two-way ANOVA was used for statistical differences ( P <.05). Dentin surfaces were examined with scanning electron microscopy (SEM) at x5000 and x10000 magnifications. Results: The higher shear bond values were observed in the groups with Teethmate Desensitizer applied and cemented with self-etch (16.05 ± 6.24 and 14.73 ± 4.75), whereas the lowest bonding values were observed in the groups with self-adhesive resin cement without Teethmate Desensitizer (3.73 ± 0.77 and 5.85 ± 4.19; P <.001). As the main effect of the treatment, the bond strength was 9.39 ± 6.04 in the control group, whereas it was 13.49 ± 5.44 in the Teethmate applied groups ( P <.05) Conclusions: Calcium phosphate desensitizer did not adversely effected shear bond strength of self-etch/adhesive resin cements to dentin. It even significantly increased the shear bond strength of self-adhesive resin cements.

Polylactic acid nanocomposites for biomedical applications: effects of calcium phosphate, and magnesium phosphate nanoparticles concentration

ABSTRACT Biodegradable polylactic acid (PLA) is synthesised from lactic acid by ring-opening polymerisation (ROP). Calcium phosphate (CaP) and magnesium phosphate (MgP) nanoparticles were incorporated into the PLA matrix to study its mechanical and rheological properties. PLA nanocomposites were prepared by the melt compounding assisted with ultrasonic vibration, and the samples were cast inside the vacuum chamber. Scanning electron microscopy photomicrographs of PLA nanocomposites show that CaP and MgP nanoparticles were well dispersed inside the matrix. The tensile strength of PLA/CaP nanocomposites increases up to 15% loading and that of PLA/MgP nanocomposites up to 2% concentration. It is also found that with respect to tensile strength, PLA/CaP and PLA/MgP nanocomposites can be used for the human bone implant. Rheological properties show that complex viscosity decreases with angular frequency but increases with nanoparticles concentration, confirming shear thinning behaviour.Storage modulus and loss modulus of PLA nanocomposites increase with angular frequency and nanoparticles concentration.

The effect of calcium phosphate and silk fibroin nanofiber tuning on properties of calcium sulfate bone cements

Calcium sulfate (CS) bone cements have been used as bone substitutes for a long time, but their clinical use is currently limited due to their rapid degradation rate and brittleness. This work aimed to study the effect of α-tricalcium phosphate (α-TCP) and silk fibroin nanofibers (SFF) on CS bone cements. The bone cements were prepared from α-CS hemihydrate (α-CSH), calcium sulfate dihydrate (CSD; as a setting accelerator) and varying α-TCP contents (0%, 5%, 10%, 15%, 20% and 25%), with SFF solution or deionized water as the solidification solution at the same liquid/solid ratio. Scanning electron microscopy, particle size distribution, x-ray diffraction and Fourier transform infrared spectroscopy were used to measure the composition and characterize the properties of the materials. The compressive strength, setting time and weight loss rate of samples were also tested. Cytotoxicity was evaluated by a Cell Counting Kit-8 assay. The results suggest that the tuning of α-TCP and SFF has an important role in determining the compressive strength and degradation rate of CS bone cements, and the properties could be changed by varying the content of α-TCP. Moreover, cell experiments showed no toxicity of the samples towards MC3T3 cells. Thus, the materials prepared from α-CSH, CSD, α-TCP and SFF in this work could provide the basis for research into CS-based bone repair materials.

In vitro degradation and mechanical behaviour of calcium phosphate coated Mg-Ca alloy

ABSTRACT The mechanical and physical properties of Mg-Ca alloys make them suitable for temporary orthopaedic implant applications. However, the rapid degradation of these alloys limits their use in the physiological environment. The effect of calcium phosphate (CaP) coating on biomineralization, biodegradation, and mechanical behaviour of the alloy in physiological environment is investigated in this work. Supersaturated calcification solution was used for developing CaP layer on the HNO3 pretreated substrate. The surface morphology and composition of phases present in the samples after immersion in supersaturated simulated body fluid were analysed using a scanning electron microscope fitted with energy dispersive spectroscopy. The results show that the CaP coating improved biomineralization and reduced the degradation rate. The CaP coating also helped in controlling the reduction in mechanical properties in the physiological environment. Hence, the CaP coating can be used as a surface modification technique to tailor the degradation rate of Mg-Ca alloys.

Effects of calcium-phosphate, laser and adhesive on dentin permeability and bond strength

ObjectivesThe present study examined a technique for reducing dentin permeability through the application of a calcium phosphate (CaP)-based desensitiser with a laser-assisted process and evaluated adhesive-dentin bond strength. Methods: Thirty dentin discs were divided into two groups according to whether the selected desensitiser (TeethMate; Kuraray Noritake) was used prior to dentin bonding. Each group was subdivided into three subgroups (n = 5): A- Adhesive (Single Bond Universal, 3M ESPE), AL- Adhesive + Laser (Nd:YAG 60 mJ) and LAL- Laser + Adhesive + Laser. Dentin permeability values (%) were recorded before and after desensitiser application. Resin composites were placed over the bonded specimens; the latter were aged prior to microtensile bond strength evaluation. Gelatinolytic activity within the hybrid layers was examined with in-situ zymography using confocal laser scanning microscopy. Data were analysed with ANOVA and Tukey test (α = 0.05). ResultsSignificant differences in dentin permeability were identified for all groups (p = 0.00). Both laser treatment (p = 0.182) and desensitiser application (p = 0.687) did not significantly improve dentin bond strength. Ultrastructure of the resin-dentin interface identified presence of calcium phosphate within dentinal tubules. Laser treatment did not affect hybrid layer ultrastructure. Both treatment modalities (intratubular CaP occlusion and laser) had no influence on gelatinolytic activity within hybrid layers. ConclusionAlthough intratubular CaP occlusion and laser treatment were effective in reducing dentin permeability, they did not affect bond strength, interfacial ultrastructure and gelatinolytic activity within hybrid layers. Clinical relevanceTreatment of etched dentin with Nd:YAG Laser at 60 mJ does not adversely affect collagen ultrastructure and gelatinolytic activity within the hybrid layer. The application of a calcium phosphate-based desensitiser to etch dentin does not affect dentin bond strength.

Effect of Calcium Phosphate on Tensile and Rheological Properties of Polylactic Acid (PLA)

From the last few decades, biodegradable composites have become best alternatives over the petro based polymer because these degrade in the simple compound in the natural environments. Among the available biodegradable polymers, polylactic acid (PLA) is more popular due to its biocompatibility and mechanical properties, that can be used in the biomedical application, such as sutures, bone and ligament fixation screws etc. In this study, synthesis of PLA was performed by ring opening polymerization and Calcium phosphate/Polylactic acid (PLA) bio-composites were prepared by melt mixing technique. Tensile properties of these composites are investigated to assess its feasibility in biomedical and food packaging application.

Chitosan microparticles based polyelectrolyte complex scaffolds for bone tissue engineering in vitro and effect of calcium phosphate

Chitosan microparticles were mixed with chitosan and carboxymethyl cellulose solution to achieve a good binding between the microparticles. Three different compositions of scaffolds were made by varying the calcium phosphate (CaP) amount: 0%, 10%, and 20%. Potassium chloride was used as salt, to make pores inside the scaffolds after leaching out when immersed in phosphate buffer saline (PBS). Compressive strength and compressive modulus of both non-porous (before leaching out), and porous (after leaching out) scaffolds were measured according to the ASTM standards. The highest compressive strength of 27 MPa was reported on 10% CaP scaffolds while 20% CaP scaffolds showed the lowest. The increasing CaP content reduces the compressive strength of the scaffolds. The highest wet state compressive strength was reported on 0% CaP scaffolds with 0.36 MPs and 0.40 MPa at day 1 and day 3 respectively. In vitro cell culture studies showed good cell adhesion and cell proliferation on 10% CaP scaffolds.

Oxalate induces mitochondrial dysfunction and disrupts redox homeostasis in a human monocyte derived cell line

Monocytes/macrophages are thought to be recruited to the renal interstitium during calcium oxalate (CaOx) kidney stone disease for crystal clearance. Mitochondria play an important role in monocyte function during the immune response. We recently determined that monocytes in patients with CaOx kidney stones have decreased mitochondrial function compared to healthy subjects. The objective of this study was to determine whether oxalate, a major constituent found in CaOx kidney stones, alters cell viability, mitochondrial function, and redox homeostasis in THP-1 cells, a human derived monocyte cell line. THP-1 cells were treated with varying concentrations of CaOx crystals (insoluble form) or sodium oxalate (NaOx; soluble form) for 24h. In addition, the effect of calcium phosphate (CaP) and cystine crystals was tested. CaOx crystals decreased cell viability and induced mitochondrial dysfunction and redox imbalance in THP-1 cells compared to control cells. However, NaOx only caused mitochondrial damage and redox imbalance in THP-1 cells. In contrast, both CaP and cystine crystals did not affect THP-1 cells. Separate experiments showed that elevated oxalate also induced mitochondrial dysfunction in primary monocytes from healthy subjects. These findings suggest that oxalate may play an important role in monocyte mitochondrial dysfunction in CaOx kidney stone disease.

Calcium phosphate surface treatment of bioactive glass causes a delay in early osteogenic differentiation of adipose stem cells

Human adipose stem cells (ASCs) combined with osteostimulative material provide an attractive approach for clinical bone regeneration. The effect of calcium phosphate (Ca-P) surface treatment of three-dimensional bioactive glass scaffolds on the attachment, proliferation, and osteogenic differentiation of ASCs was studied. Three types of bioactive glass scaffolds (nontreated, thick and thin Ca-P treated) were compared. All scaffold types supported ASC attachment, spreading, and proliferation equally as detected by scanning electron microscopy, fluorescence staining, and DNA measurement. Indices of osteogenic differentiation including the expression of osteopontin and alkaline phosphatase (ALP) were consistently higher in the nontreated and thin Ca-P-treated scaffolds when compared with thick Ca-P-treated scaffolds at 2 weeks. ASCs cultured on nontreated bioactive glass scaffolds showed significantly higher ALP activity when compared with both thin and thick Ca-P-treated scaffolds after 1 week in culture, but these differences equalized between the three scaffolds by the 2-week time point. In conclusion, osteogenic differentiation appears to be delayed on the Ca-P surface-treated scaffolds. This delay is more pronounced with thick Ca-P treatment of the scaffolds.

Infrared Spectroscopic Studies on the Dipalmitoyl Phosphatidylcholine Bilayer Interactions with Calcium Phosphate: Effect of Vitamin D2

In the present work, the interaction of calcium‐phosphate with DPPC (dipalmitoyl phosphatidylcholine) model membranes has been studied in the presence and absence of vitamin D2 by using Fourier Transform Infrared (FTIR) spectroscopy. Calcium and phosphorus are the most abundant elements in the body. They combine in the form of calcium phosphate salt, called hydroxyapatite. Hydroxyapatite is the major structural component of the bone. Calcium phosphate assists with the digestion and absorption of food and is vitally important for the building of sturdy bone and body structures and a robust constitution. Phosphorus is extracted from foods and its use is controlled by vitamin D and calcium. FTIR spectral analysis results suggested that, calcium–phosphate complex, which is the major component of the bones, decreases the phase transition temperature to lower values, causes a loss in cooperativity of the acyl chains, decreases the order of the membrane in both phases and decreases the dynamics of the membrane in the liquid crystalline phase, increases the flexibility of the chains in the center of the bilayer in both phases, and increases the mobility of the head group of DPPC in the gel phase. The effect of calcium‐phosphate on DPPC liposomes diminishes with the addition of vitamin D2 into the liposomes. Our results suggest how calcium‐phosphate and/or vitamin D2, which have indispensable role for the functioning of the bone tissue, affect the thermal behaviour of DPPC liposomes at molecular level.

Local tissue irritating effects and adjuvant activities of calcium phosphate and aluminium hydroxide with different physical properties

Effects of calcium phosphate and aluminium hydroxide adjuvants with different physical properties were examined in guinea pigs for local histopathological reactions, electron-microscopical changes of macrophages and adjuvanticity on total IgG antibody response to subcutaneously administered ovalbumin (OVA) and tetanus toxoid (TT). Calcium phosphate gel (Ca-gel) induced active inflammatory reactions consisting of neutrophils (pseudoeosinophils) and foamy macrophages associated with many multinuclear giant cells for at least 4 weeks. Aluminium hydroxide gel (Al-gel) also elicited granulomatous inflammatory reactions consisting mainly of macrophages with foamy cytoplasm, small lymphocytes and giant cells at the injection sites for up to 8 weeks or longer. Severity of local tissue irritation due to calcium phosphate gel (Ca-gel) was similar to that due to Al-gel except for the duration of the inflammatory reactions. Calcium phosphate suspension (Ca-sus)-induced local reactions completely ceased by the 4th week, while aluminium hydroxide suspension (Al-sus)-induced reactions were seen up to the 8th week. Electron-microscopical observations showed that both Al-gel and Al-sus caused damage of macrophages. The adjuvant activity of Al-gel for OVA or TT was significantly stronger than that of any other adjuvant material, whereas those of Ca-gel and Ca-sus were not seen at a dose of 3 mg calcium phosphate per millitre. Al-sus-TT at a dose of 3 mg aluminium hydroxide per millilitre induced very low levels of antibody. These results suggest that calcium phosphate adjuvant may not be an useful alternative to Al adjuvant.

Effect of calcium phosphates and zinc in salt-mineral mixtures on ad libitum salt-mix intake and on zinc and selenium status of sheep.

In two separate experiments, 72 crossbred ewes were fed hay, haylage (50% dry matter) and corn diets with ad libitum salt-mineral mixtures (SMM; Exp. 1) or salt (Exp. 2). Calcium phosphates (Ca X P) and(or) zinc (Zn) were added in a 2 X 2 factorial arrangement to salt + trace minerals for ewes 7 mo prepartum through lactation in Exp. 1 and to salt only for ewes 3 mo prepartum through lactation in Exp. 2. The diets fed were estimated to contain 23 and 28 mg Zn/kg dry diet (ppm), respectively, and .08 and .05 ppm Se. Large variations (up to fivefold) were found in SMM intake per month between replicates and from month-to-month within treatment; thus, monthly variations of up to sevenfold occurred in Zn and Se intakes of supplemented groups. There were no significant treatment effects on SMM intake. Small but significant Zn treatment effects were detected for plasma and wool Zn of ewes and lambs, but all values were in the normal range. There was no significant treatment effect on plasma alkaline phosphatase activity. In Exp. 2, erythrocyte glutathione peroxidase (GSH-Px) activity was significantly lower in all treatment groups compared with a Se-supplemented control group but only rare occurrences of subclinical muscular dystrophy were found. There was no significant treatment effect on GSH-Px activity, whole blood Se in ewes and lambs or plasma creatine phosphokinase activity in lambs. These results indicate large animal and seasonal variability in SMM intake and no significant treatment effects of Ca X P on SMM intake or on Zn and Se status. Zinc addition to SMM had no effect on Se status.

Effect of calcium phosphate and alumina C gamma gels on the mutagenicity and cytotoxicity of dimethylnitrosamine as studied in the CHO/HGPRT system.

When CaCl2 was added in increasing concentrations to a rat liver metabolic activation system (S9) buffered with sodium phosphate, the mutagenic activity and cytotoxicity of dimethylnitrosamine (DMN) in the Chinese hamster ovary cell/hypoxanthine-guanine phosphoribosyl transferase (CHO/HGPRT) system were greatly increased. This effect was not observed with an S9 mix buffered with N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES). The calcium phosphate gel precipitate of the S9 mix possessed approximately 1/3 of the total activity of the mix, while the supernatant had only slight activity. However, when the calcium phosphate gel precipitate of a solution of S9 salts (without S9 protein) was added to the supernatant, the remaining 2/3 of the activity was recovered. Commercially obtained calcium phosphate, tricalcium phosphate, and alumina C gamma gels could substitute for CaCl2 in the S9 mix, but diethylaminoethyl cellulose (DEAE cellulose) could not. Alumina C gamma gel can exert its effect in the absence of both CaCl2 and phosphate in the S9 mix. Increasing the time of contact between the S9 protein and the S9 salts increased the efficacy with which the S9 mix activated DMN; this is indicative of an adsorptive process by calcium phosphate gel.

Effects of Sequential Calcium Phosphate- Fluoride Rinses on Fluoride Uptake in Rats

This study measured the effects of a calcium phosphate rinse followed by various fluoride rinses on fluoride uptake by enamel in rats. Calcium phosphate rinses promoted fluoride uptake by the enamel.

Effect of calcium phosphate on thrombin and on its sensitivity to heparin and antithrombin-III

Thrombin was inactivated by antithrombin-III and the rate of inactivation was accelerated by heparin either in 0.04 M sodium phosphate buffer or in 0.04 M Tris-HCl buffer, at pH 7.4. Calcium chloride, at a final concentration of 1 mM, influenced slightly thrombin inactivation by both antithrombin and antithrombin plus heparin in Tris-HCl buffer, whereas in phosphate buffer the sensitivity of enzyme to antithrombin and heparin decreased. Thrombin showed also increased stability against the inactivating effect of heat at 54°C in sodium phosphate buffer containing calcium chloride. These findings suggest that thrombin bound to calcium phosphate is extremely stable against inactivation by antithrombin and heparin, while its clotting activity does not change. This nature of enzyme may play a role in predisposition for thrombosis during arteriosclerosis.

The Effect of Calcium Phosphate on Dental Caries in School Children

The Effect of Calcium Phosphate on Dental Caries in School Children

The Effect of Calcium Phosphate on Dental Caries in School Children

The Effect of Calcium Phosphate on Dental Caries in School Children