Carbonate Apatite Research Articles

Enhancement of carbonate apatite scaffold properties with surface treatment and alginate and gelatine coating

Carbonate apatite (CO3Ap) scaffolding has been widely used for bone repair and replacement due to its excellent osteoconductivity and resorbability in bone defects. However, the application of the porous scaffold has been limited by its brittleness. Here, CO3Ap scaffolds coated with 1, 3 and 5 wt% of sodium alginate (SA) and bovine gelatine (BG) were fabricated to improve the mechanical properties of the porous scaffold. Limited studies have been done on a CO3Ap scaffold coated with a natural polymer layer. Here, a CO3Ap scaffold was fabricated through the phase transformation from β-tricalcium phosphate (β-TCP) to CO3Ap using a hydrothermal method. Fourier-transform infrared (FTIR) analysis confirmed the presence of both SA and BG functional groups on the CO3Ap scaffold. Five wt% of SA and BG improved the compressive strength of the uncoated CO3Ap scaffold by 34% and 46%, respectively. The SA coating was found to enhance the compressive strength of the CO3Ap scaffold compared to the BG coating due to its high viscosity. Furthermore, the compressive strength of the scaffold increased by 40% after undergoing a silanization process and being coated with SA. These results indicate that the use of a silane treatment improved the chemical bonding between the CO3Ap scaffold and SA coating. This process increased the adhesion between the SA coating and the scaffold and improved the compressive strength.

Krebs Cycle Intermediate-Modified Carbonate Apatite Nanoparticles Drastically Reduce Mouse Tumor Burden and Toxicity by Restricting Broad Tissue Distribution of Anticancer Drugs.

The morphology, size, and surface area of nanoparticles (NPs), with the existence of functional groups on their surface, contribute to the drug binding affinity, distribution of the payload in different organs, and targeting of a particular tumor for exerting effective antitumor activity in vivo. However, the inherent chemical structure of NPs causing unpredictable biodistribution with a toxic outcome still poses a serious challenge in clinical chemotherapy. In this study, carbonate apatite (CA), citrate-modified CA (CMCA) NPs, and α-ketoglutaric acid-modified CA (α-KAMCA) NPs were employed as carriers of anticancer drugs for antitumor, pharmacokinetic, and toxicological analysis in a murine breast cancer model. The results demonstrated almost five-fold enhanced tumor regression in the cyclophosphamide (CYP)-loaded α-KAMCA NP-treated group compared to the group treated with CYP only. Also, NPs promoted much higher drug accumulation in blood and tumor in comparison with the drug injected without a carrier. In addition, doxorubicin (DOX)-loaded NPs exhibited less accumulation in the heart, indicating less potential myocardial toxicity in mice compared to free DOX. Our findings, thus, conclude that CA, CMCA, and α-KAMCA NPs extended the circulation half-life and enhanced the anticancer effect with reduced toxicity of conventional chemotherapeutics in healthy organs, signifying that they are promising drug delivery devices in breast cancer treatment.

Does Stone Analysis Have Better Predictive Value Than Urine Culture and Stone Culture for Predicting Systemic Inflammatory Response Syndrome Post Retrograde Intra Renal Surgery? A Single Center Pilot Study

Purpose: Infective complications such as fever, systemic inflammatory response syndrome (SIRS), septicemia, and shock are common and preventable complications after retrograde intrarenal surgery (RIRS). Patients with positive urine and stone cultures have a greater risk of SIRS. Infection stones (carbonate apatite) are bacteria-harboring stones that predispose to sepsis. A pilot study is conducted to establish the role of stone analysis in predicting SIRS after RIRS compared to urine and stone cultures. Materials and Methods: Sixty patients who underwent RIRS from January 2018 to June 2018 were prospectively evaluated with respect to preoperative urine culture, stone burden and location, operative time, postoperative clinical course, residual stone size, stone culture, stone analysis, and occurrence of septicemia-related events. Results: 5 out of 60 patients who underwent RIRS developed SIRS (8%). Sensitivity levels of predicting SIRS were different, where urine culture (20%), stone culture (20%), and carbonate apatite on the stone analysis (60%). Positive urine culture and stone culture had no significant relation to the prediction of SIRS (P = 1). Carbonate apatite was present in 12 samples (20%) in varying proportions. The presence of apatite >50% of the total sample was in 5/60 samples (8%), which are referred to as infection stones. Three out of these 5 patients with infection stones developed SIRS (60%). Thus, the presence of carbonate apatite in the stone analysis had a statistically significant relation to SIRS (P < 0.01). Conclusion: The presence of carbonate apatite >50% on stone analysis has higher sensitivity than urine and stone culture in predicting SIRS after RIRS.

Different Molarities and Dissolution-Precipitation Duration Affect the Formation of Carbonate-Apatite Blocks for Bone Graft Material

Objective: To determine diametral tensile strength and water absorption ability of Carbonate-apatite blocks fabricated from gypsum precursors (CaSO4) through a dissolution-precipitation method, with different solution molarities and immersion times. Material and Methods: Thirty-six CaSO4 gypsum specimens with 6 mm diameter; 3 mm height (Group A for diametral tensile strength) and 36 specimens of 6 mm diameter; 3 mm thickness (Group B for water absorption ability) were used. Each group was divided into 4 group treatments of: 1) dissolution-precipitation in solution of 0.5mol / L Na 2 CO 3 + 0.5mol / L Na 3 PO 4 for 48 hours and 72 hours; 1mol / L Na 2 CO 3 + 1mol / L Na 3 PO 4 for 48 hours and 72 hours. The C-Ap blocks were then tested using ATR-FTIR spectrometer to identify the formation of C-Ap functional groups. Furthermore, Group A specimens were tested for diametral tensile strength using Universal Testing Machine, and Group B specimens were tested for water adsorption ability using an analytical balance by measuring initial and final weight after immersion in saline solution at 37 o C for 24 hours . Results: The formation of carbonate-apatite (C-Ap) in groups with solution molarity of 1 mol/L for 48 hours and 72 hours resulted in a lower diametral tensile strength and water absorption ability than the groups with a 0.5 mol/L solution . Conclusion: Solution with different molarities and dissolution-precipitation duration affect the formation of carbonate-apatite blocks.

The biology of vascular calcification.

Vascular calcification (VC), characterized by different mineral deposits (i.e., carbonate apatite, whitlockite and hydroxyapatite) accumulating in blood vessels and valves, represents a relevant pathological process for the aging population and a life-threatening complication in acquired and in genetic diseases. Similarly to bone remodeling, VC is an actively regulated process in which many cells and molecules play a pivotal role. This review aims at: (i) describing the role of resident and circulating cells, of the extracellular environment and of positive and negative factors in driving the mineralization process; (ii) detailing the types of VC (i.e., intimal, medial and cardiac valve calcification); (iii) analyzing rare genetic diseases underlining the importance of altered pyrophosphate-dependent regulatory mechanisms; (iv) providing therapeutic options and perspectives.

Oral priming with oligodeoxynucleotide particles from Lactobacillus rhamnosus GG attenuates symptoms of dextran sodium sulfate-induced acute colitis in mice.

Here, we investigated the effect of prophylactic oral treatment with carbonate apatite-based particles (ID35caps) containing Lactobacillus rhamnosus GG-derived immunostimulatory oligodeoxynucleotides (ID35) when used in mice with acute colitis. Mice were administered orally with control particles (carbonate apatite particles, Caps), ID35, or ID35caps for 2days, and then were given free access to drinking water containing 3% (w/v) dextran sodium sulfate (DSS) for 5days (Days 0-5) to induce acute colitis. Body weight change, fecal bleeding, and stool consistency were monitored and scored as a disease activity index (DAI) to assess symptoms of colitis. On Day 10, animals were euthanized and the colon length was measured to evaluate inflammatory tissue injury. Prophylactic oral treatment with ID35caps significantly suppressed DSS-induced elevation of the DAI score and shortening of the colon compared to the respective parameters in DSS-exposed mice treated with Cap or ID35. We conclude that oral priming with ID35caps attenuates symptoms and inflammatory colonic injury in a mouse model of DSS-induced acute colitis. This finding suggests that ID35caps may be a new oral agent for preventing intestinal inflammation.

Insights into OCP identification and quantification in the context of apatite biomineralization

Monitoring apatite formation throughin situRAMAN andex situssNMR spectroscopy.

Proliferation of Mesenchymal Stem Cells in Carbonate Apatite-Chitosan Scaffolds in Bone Tissue Engineering Techniques

Objectives: Chitosan (poly-1,4-D-glucosamine) become popular as bone graft material. It has a high biocompatibility and biodegradability, non-toxic, bacteriostatic, and has good adsorption properties. It also enhances the proliferation and differentiation of the osteoblast cell cultures. However, chitosan also has a weakness for cell adhesion and the lack of sufficient bone formation capabilities. To improve it, we tried to develop a chitosan scaffolds that combine with carbonate apatite (CA), which has excellent biocompatibility properties of the tissues of the human body. Purpose: to make the carbonate apatite-chitosan scaffolds (CA-ChSs) and evaluate CA-ChSs from the standpoint of cell proliferation using mesenchymal stem cells (MSCs). Materials and Methods: Porous chitosan matrix was made by using the lyophilization technique. ChSs containing chitosan powder was made by the following procedure. 100, 150, 200, and 400 mg of chitosan powder was dissolved in 5 ml of 2% acetic acid at room temperature. To make CA-ChSs, ChSs containing 200 mg of chitosan powder was chosen. Ultraviolet radiation was then performed for 2 hours. CA-ChSs structure was observed by a scanning electron microscope (SEM). Proliferation of MSCs in CA-ChSs evaluated at days 1, 3, 5 and 7.Results:This study demonstrated that CA-ChSs containing 200 mg of chitosan powder and 50 mg CA has a three-dimensional structure that is porous and attachment powder CA in the pores and absorbance values were increased from the examination day 1 until day 7. Conclusion:Based on these results, it is expected CA-ChSs may be candidates for bone graft material in tissue engineering techniques.

Fabrication of porous carbonate apatite granules using microfiber and its histological evaluations in rabbit calvarial bone defects.

Carbonate apatite (CO3 Ap) granules are known to show good osteoconductivity and replaced to new bone. On the other hand, it is well known that a porous structure allows bone tissue to penetrate its pores, and the optimal pore size for bone ingrowth is dependent on the composition and structure of the scaffold material. Therefore, the aim of this study was to fabricate various porous CO3 Ap granules through a two-step dissolution-precipitation reaction using CaSO4 as a precursor and 30-, 50-, 120-, and 205-μm diameter microfibers as porogen and to find the optimal pore size of CO3 Ap. Porous CO3 Ap granules were successfully fabricated with pore size 8.2-18.7% smaller than the size of the original fiber porogen. Two weeks after the reconstruction of rabbit calvarial bone defects using porous CO3 Ap granules, the largest amount of mature bone was seen to be formed inside the pores of CO3 Ap (120) [porous CO3 Ap granules made using 120-μm microfiber] followed by CO3 Ap (50) and CO3 Ap (30). At 4 and 8 weeks, no statistically significant difference was observed based on the pore size, even though largest amount of mature bone was formed in case of CO3 Ap (120). It is concluded, therefore, that the optimal pore size of the CO3 Ap is that of CO3 Ap (120), which is 85 μm.

Fabrication and Histological Evaluation of Porous Carbonate Apatite Block from Gypsum Block Containing Spherical Phenol Resin as a Porogen.

The utility of carbonate apatite (CO3Ap) as a bone substitute has been demonstrated. The feasibility of fabricating macroporous CO3Ap was evaluated through a two-step dissolution–precipitation reaction using gypsum as the precursor and spherical phenol resin as the porogen. Porogen-containing gypsum was heated to burn out the porogen and to fabricate macroporous structures. Gypsum transformed into CaCO3 upon immersion in a sodium carbonate solution, while maintaining its macroporous structure. Next, CaCO3 transformed into CO3Ap upon immersion in a Na2HPO4 solution while maintaining its macroporous structure. The utility of the macroporous CO3Ap for histologically reconstructing bone defects was evaluated in rabbit femurs. After 4 weeks, a much larger bone was formed inside the macroporous CO3Ap than that inside non-macroporous CO3Ap and macroporous hydroxyapatite (HAp). A larger amount of bone was observed inside non-macroporous CO3Ap than inside macroporous HAp. The bone defects were completely reconstructed within 12 weeks using macroporous CO3Ap. In conclusion, macroporous CO3Ap has good potential as an ideal bone substitute.

The Use of Sucrose Granule as Pore Maker in Preparation of Porous Calcium Sulfate Dihydrate

Calcium sulfate dihydrate (CSD) has been clinically used as bone filler for decades. CSD bone graft is cheap, biocompatible and can be transformed to other osteoconductive ceramics such as hydroxyapatite and carbonate apatite. In addition, porous ceramic bone grafts is desired clinically. Development of porous ceramics bone graft with simple and cost-effective method is preferred. Thus, in this study, porous CSD was developed. Porous CSD can be used both as bone filler or precursor for porous hydroxyapatite and carbonate apatite. Porous CSD was prepared by mixing calcium sulfate hemihydrate (CSH) containing sucrose granules with distilled water. After setting, the sucrose granules were removed by immersion in distilled water. Porous CSD was obtained after sucrose leaching. It was observed that more pore formed in the specimen with 50% sucrose granule compared with that of 25% sucrose granule. The sucrose was completely removed from the porous CSD evident from ATR-FTIR analysis. The diametral tensile strength of the porous CSD tend to decrease with the increase of sucrose granule. Finally, sucrose granule was feasible to be used as pore maker in preparation of porous CSD.

The Effect of Platelet Rich Fibrin (PRF) and Bone Graft (Carbonate Apatite) Applications on Platelet Derived Growth Factor-BB Post Flap Surgery in Patients with Chronic Periodontitis

Chronic periodontitis characterized by a periodontal pocket over 5 mm, alveolar bone resorption accompanied by tooth mobility, requires periodontal surgical treatment. Conventional surgical treatment can not achieve the regeneration of periodontal tissue and thus requires regenerative procedures, such as with the addition of PRF. PDGF-BB is a growth factor that plays an important role in wound healing. Developments in additional bioactive ingredients in surgical procedures are used to regulate inflammation and increase the speed of the healing process. The purpose of this study was to determine the effect of PRF and bone graft (carbonate apatite) on PDGF-BB levels post-surgical flap in patients with chronic periodontitis. The experimental study with open label and consecutive sampling was conducted on 10 subjects of chronic periodontitis who received surgical flap treatment with bone graft and PRF; and 10 subjects without PRF. GCF samples were collected immediately before surgery and 7 days post flap surgery for examination of PDGF-BB levels by ELISA method. The data were calculated statistically by Mann-Whitney test (p <0.05). The results showed that the mean difference of PDGF-BB level in PRF group was 9.44 pg/ml (-1.20 – 37.79 pg/ml) with p value (0.013) and Non-PRF group was 7.97 pg/ml (-6.62 - 44.42 pg/ml) with p value (0.059). The p value in the PRF group > 0.05 means a significant increase in PDGF-BB levels on the 7th day post flap surgery. Examination of PDGF levels, especially PDGF-BB, should be done in each healing phase of the wound from the inflammatory phase to the maturation and remodeling phase, for example on the 3rd, 7th, 14th and 28th days when PDGF levels approach zero and the healing process it's almost over, referring to the results of Alzahrani's research (2018) and also Matsuoka and Grotendorst (1989) which showed higher levels of PDGF-BB and VEGF in GCF on days 1, 3, 7 and 14 after surgery with minimally invasive surgery (MIS) technique. The conclusions of this study showed that the application of Platelet Rich Fibrin (PRF) and bone graft had an effect on the level of Platelet Derived Growth Factor (PDGF-BB) post-surgical flap in patients with chronic periodontitis, and elevated levels of PDGF-BB post-surgical flap with PRF application higher than surgical flap without the PRF application. Increased levels of PGDF-BB in the group applied to the PRF were higher than those that were not applied PRF, although statistically significant differences were not found, there was a tendency for the healing process of the PRF group to be better than the Non PRF group.

The Effect of Combination Platelet Rich Fibrin (PRF) with Bone Graft (Carbonate Apatite) to Vascular Endothelial Growth Factor (VEGF) Level: Tissue Engineering Research

Platelet Rich Fibrin (PRF) is a platelet that contains growth factor, such Vascular Endothelial Growth Factor (VEGF) that not only have implication in inflammation, stimulate tissue healing but also bone regeneration. The aim of this study was to evaluate the effect of combination PRF with bone graft (carbonate apatite) to VEGF level. This research is an experimental study, with consecutive sampling technique. This research was conducted by selecting 20 subjects (12 male, 8 female) which divided into two groups; 10 subjects in the treatment group were given bone graft and PRF application while another 10 subjects in the control group were given only bone graft without PRF application. The measurement of VEGF level was taken by inserting the paper point no.30 into sulcus before the surgery (D0) and one week after surgery (D7). VEGF level was assessed by ELISA method. All collected data were analyzed by using Wilcoxon test with p <0.05, and Mann-Whitney test with p <0.05.The treatment group, VEGF level at D0 was 3.8 pg/ml and D7 was 8,1 pg/ml. The difference in the level of VEGF was 4.3 pg/ml. The average of the control group at D0 was 4.5 pg/ml and D7 was 5.4 pg/ml, obtained the difference in the level of VEGF 0.9 pg/ml. The Mann Whitney Test analysis showed there was a significant difference between the treatment group and the control group withp-value0.038. PRF with bone graft application influence the increased level of VEGF.

Mechanical Strength and Porosity of Carbonate Apatite-Chitosan-Gelatine Scaffold in Various Ratio as a Biomaterial Candidate in Tissue Engineering

Bone defect is a common problem in the field of dentistry. The defect can be solved bytissue engineering. One component of tissue engineering is scaffold. Carbonate apatite is the main material used because it has an organic components similar to human bones. The carbonate apatite combined with gelatin and chitosan can be used as a scaffold for tissue engineering. The aim of thisstudy is to know the exact ratio of the carbonate apatite, chitosan-gelatine (CA:Ch-GEL) scaffold on the compressive strength and porosity size as biomaterial candidates in tissue engineering. Scaffold was synthesized from CA:Ch-GEL with different ratios of 50:50, 60:40, 70:30 and 80:20 withfreeze drying method. Fourier Transform Infared Spectroscopy (FTIR) was used CA:Ch-GEL scaffold functional group identification. Scaffold mechanical test was performed using an Autograph while a porosity test was performed using Scanning Electron Microscope. All data wereanalyzed by ANOVA followed by Tukey HSD test. Scaffold has a compressive strength ranges 4.02 - 11.35 MPa, with porous ranges 19,18 mm – 52,59 mm at 50:50, 60:40, 70:30 and 80:20 ratios. CA:Ch-GEL scaffold at all ratios can be used as biomaterials in tissue engineering

Apatite Formation on Zirconia (Y-TZP) Coated with Carbonate Apatite in Simulated Body Fluid

Abstract. Various bioactive calcium phosphates such as hydroxyapatite (HA) and carbonate apatite (CO3Ap) have been widely studied due to their biocompatibility and osteoconductivity when implanted into bone defects. CO3Ap has the ability to adapt bone structure and induce bone regeneration; so that it can be categorized as resorbable bioactive materials. CO3Ap induced much stronger response such as cell adhesion and actin ring formation to osteoclast-like cells rather than HA. The aim of this study is to evaluate the bioactivity on zirconia (Y-TZP) coated with CO3Ap using simulated body fluid (SBF). Twenty Y-TZP ZrO2 disks with a 12-mm diameter and 1-mm thickness were employed as the samples. The disks were divided into two groups which the control group without CO3Ap coating and tested group with CO3Ap coating. Disks samples are dipped into CO3Ap suspension for one minute and stored in 37°C incubator for 24 hours. The disks were soaked in SBF for 1, 4, and 7 day(s) at 36.5°C. The obtained apatite crystals were characterized by scanning electron microscopy (SEM). It was found that the apatite formation on the tested group was greater than the control group. The EDS pattern showed the presence of Ca and P on the control and tested group after SBF soaking, which indicate the apatite deposition on the disks’ surface. However, the Ca and P on the tested group was higher compared to the control group. The formation of apatite layer on the disks’ surface is bioactivity indicator of CO3Ap.

Diametral Tensile Strength Evaluation of Carbonate Apatite Cement Reinforced by Genipin Cross-Linked Gelatin

Carbonate apatite is one of the most widely studied bioceramic material for its use as bone cement. On the previous study, it has already stated that CO3Ap cement has good osteoconductivity which makes this cement could be replaced by bone. However, the mechanical strength of CO3Ap cement is still low. This low mechanical strength is estimated due to the high porosity and absence of organic components. The aim of this study is to improve the mechanical strength of the CO3Ap cement reinforced by gelatin as an organic component with genipin as a cross-linking agent (Gelapin). The powder phase of vaterite and DCPA at weight ratio 40:60 were mixed with 0.2 mol/L Na2HPO4, 5% (w/v) gelatin, and 20% (v/v) genipin using 0.5 liquid to powder (L/P) ratio. The liquid phase ratios of Na2HPO4 and Gelapin were 50:50, 70:30, and 90:10. For control group, Gelapin were didn’t mixed in the liquid. Diametral tensile strength was improving and statistically significant (p<0.05) on set cement with 50:50 liquid ratio, the average value was 6.02 ± 0.14 MPa whereas the average value of the control group was only 3.10 ± 0.15 MPa. For this instance, gelatin serves a polymer matrix so the carbonate apatite crystallites could be well distributed within it which then gives more flexibility and resistance for the cement. On the other hand, genipin was also successfully cross-linked the gelatin. This study showed that by reinforcing CO3Ap cement using genipin cross-linked gelatin might be a good candidate for a bone substitute material.

Characterization of Zirconia for Ceramic Dental Implant Coated with Carbonate Apatite

Zirconia-based dental implant in Indonesia is rarely used, especially due to low demand. High production cost makes the price of each zirconia dental implant piece become expensive. The fabrication process of the dental implant using 3 mol% Yttria-stabilized Zirconia (3YSZ) as a starting powder, or being synthesized using ZrCl3 and YCl4 precursor were costly and complicated. The aim of this study is to investigate morphology and phase analysis in the ceramic dental implant which coated with carbonate apatite (CO3Ap). The industrial 3YSZ powder was compacted using a manual hydraulic press and sintered at 1500°C approximately to 11 mm pellet size. Specimens were pre-treated using 9% hydrofluoric acid (HF) before coated by CO3Ap, while others without treatment as a control. Then, the specimens were dipped into CO3Ap suspension and heat treated with temperature variable of 300°C or 500°C. The fabrication of specimen using manual hydraulic press creates monoclinic phase more than expected, while SEM discovered that the particle size of the specimen was 130-500nm. In conclusion, the effective method to coat the ceramic dental implant with CO3Ap was using 9% HF as a pre-treatment and calcinate in 300°C as confirmed in XRD and EDS.

The Flexural Strength of Y-TZP Coated with Carbonate Apatite for Dental Implant Material

In order to gain acceleration of the osseointegration process after implant placement, micro retention using inorganic elements such as Hydroxyapatite (HA) were commonly used as a coating material in dental implant. Meanwhile, another inorganic material such as Carbonate Apatite (CO3Ap) has been known as bone substitute for decades. The purpose of this study is to investigate the flexural strength of Yttria-Stabilized Zirconia (Y-TZP) as dental implant material after being coated with CO3Ap. Ten specimens of Y-TZP were divided into two groups. The first group was coated with CO3Ap while other groups without coatings were used as the control. Biaxial flexural strength was determined using piston on three balls-technique and data were evaluated by statistical analysis. The specimens surface were analyzed through images taken by Scanning Electron Microscope (SEM). As the result, this study showed that there was no statistically significant found between the group with coating and the control group (p>0.05). The biaxial flexural strength’s mean of the group with coating and control were 212.80 MPa and 209.35 MPa; while micro Vickers hardness’ means were 229.56 HV and 245.40 HV. It can be concluded that there was no difference in the mean flexural strength between Y-TZP before and after coating.

Neogene Metasomatism in the Subcontinental Lithosphere beneath SE Asia—Evidence from Modal and Cryptic Phosphorus Enrichment in Peridotites and Pyroxenites from Southern Laos

AbstractMetasomatism is the prime process to create compositional heterogeneity of the upper mantle. Mineralogical and mineral chemical changes of the mantle triggered by metasomatism can be used to deduce the nature of the metasomatic agent(s) and to constrain the timing of metasomatism. This information is vital for an understanding of the secular evolution of a given mantle segment and the magmatic processes occurring therein. For this study spinel-lherzolites and -websterites were collected from ∼16 Myr old alkali-basaltic lava flows that were extruded on the Bolaven Plateau in south–central Laos. These xenoliths are fragments of the shallow continental lithosphere of the SE Asian peninsula and originate from a mantle segment that acted as source for Cenozoic basaltic volcanism in the wake of the India–Asia collision. In both rock types modal metasomatism formed apatite ± whitlockite ± phlogopite ± calcic amphibole ± calcite ± orthopyroxene. The principal metasomatic phase is apatite, which appears in three varieties. Type-I apatite is ±inclusion-free and associated with phlogopite, calcic amphibole, calcite and lamellar orthopyroxene. It is high in Na and low in P and shows low analytical totals indicating a type-B carbonate–apatite component. Type-I apatite presumably precipitated from a P-alkali-rich mixed H2O–CO2 fluid with low large ion lithophile element (LILE)–light rare earth element (LREE) contents. Type-II apatite shows a spongy texture and has lower Na and higher P contents with higher analytical totals. Crosscutting discontinuous zones of type-II characteristics within type-I apatites indicate type-II formation through an exchange Na+ + CO32– = PO43– + Ca2+ by a later fluid with lower aCO2. REE-rich type-III apatite is the youngest type and formed by infiltration of basaltic melts as part of spongy rims around clinopyroxene. One lherzolite contains whitlockite in addition to apatite. Whitlockite formation is ascribed to a short-lived metasomatic event involving a fluid with extremely low aH2O. Disequilibrium between whitlockite and the bulk assemblage is indicated by hydrous silicates in the immediate vicinity of whitlockite and by substantial H2O contents of 250–370 µg g–1 in clinopyroxenes and 170–190 µg g–1 in orthopyroxenes. High-density (1·15–≥1·17 g m–3) CO2–fluid inclusions in the whitlockite-bearing sample provide evidence for the presence of low-aH2O fluids at mantle depths. The spinel-herzolites may also show cryptic metasomatism evidenced by P zoning in olivine, which is characterized by P-poor (<20–130 µg g–1) cores and P-rich (170–507 µg g–1) rims, the latter in part with oscillatory zoning on a µm scale. Element correlations indicate [4]Si4+ + [6](Mg, Fe)2+ = [4]P5+ + [6]Li+, 2 [4]Si4+ + 4 [6](Mg, Fe)2+ = 2 [4]P5+ + 3 [6](Mg, Fe)2+ + [6]vac and/or 5 [4]Si4+ = 4 [4]P5+ + [4]vac as major P incorporation mechanisms. High P–T experiments conducted at 2 GPa and 950–1050 °C yield apatite-saturated P contents of olivine in the range ∼360–470 µg g–1. Most P concentrations in olivines from the xenoliths including those in the P-rich rims, however, are significantly lower than the apatite-saturated values, which indicates disequilibrium uptake of P during growth of the P-rich rims by dissolution–reprecipitation. Diffusion modeling indicates that the P zoning must have formed within decades prior to the eruption of the host basalts. This is consistent with the preservation of Li disequilibrium partitioning between olivine and pyroxenes in some of the xenoliths. All metasomatic phenomena were assigned to two metasomatic events, both of which were in close temporal relation with the eruption of the xenolith host basalts: an older event-1 formed type-I apatite, hydrous silicates, calcite and orthopyroxene and caused the modification of type-I apatite composition towards that of type-II. It is also likely to be responsible for whitlockite formation and P zoning in olivine. A younger event-2 comprises all paragenetic, textural and compositional modifications of the xenolith assemblages associated with the infiltration of basaltic melts.

The effect of carbonate apatite membrane gelatin application on IL-1β level gingival crevicular fluid in chronic periodontitis patients

Introduction: Apatite carbonate material plays an important role in bone tissue regeneration. The use of this membrane is expected to achieve better treatment success than those without additional therapy. The antimicrobial content in the apatite carbonate membrane can be used to support periodontal treatment of chronic periodontitis after scaling and root planing. The purpose of this research was to analyse the effect of carbonate apatite membrane gelatin application on the IL-1β level of the gingival crevicular fluid in chronic periodontitis patients. Methods: This research was a double-blind, randomised controlled trial method, with purposive sampling, and split-mouth design. The parameter was the IL-1β level in the gingival crevicular fluid before and after scaling and root planing. Carbonate apatite membrane gelatin was applied to the periodontal pocket on the test group after scaling and root planing. Data were analysed by the Wilcoxon test with a p-value < 0.05. Results: The reduction of IL-1β level gingival crevicular fluid on day-0 and day-30 on both groups showed significant value (p < 0.001). However, it showed no significant differences statistically, between the test group and the control group. Conclusion: Carbonate apatite membrane gelatin application might reduce the IL-1β level of the gingival crevicular fluid, but not showing a better reduction from the control group.Keyword: Carbonate apatite membrane gelatin, IL-1β, periodontal therapy