Effects of direct therapeutic radiation on pulpal surface of root dentin: an in vitro study.

The aims of the study were to analyze the effects of therapeutic radiation on human root dentin samples from the aspect of possible alterations in crystallinity, micro-morphology, and composition. Fifty-six root dentin specimens were divided into seven groups (0, 10, 20, 30, 40, 50, and 60 Gy). Scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD) analyses were performed on pulpal surfaces of root dentin after being irradiated by 6MV photon energy. Mineral compositions, Ca/P, P/N, Ca/N ratios, and hydroxyapatite pikes were calculated. Some deuteriations on the dentin surface were observed in SEM images after 30 Gy and subsequent doses. One-way ANOVA revealed that there was no significant alteration in weight percentages of C, O, Mg, Ca, P, and N between groups. Radiation did not influence stoichiometric Ca/P, Ca/N, and P/N molar ratios. XRD analysis did not show a remarkable decline in hydroxyapatite pikes by the increasing doses. Radiotherapy changes the micromorphology of circumpulpal dentin but does not affect elemental composition and crystallinity.

Fish otoliths as biological dosimeter: internal dose calculation.

Otoliths are organs used by fish for hearing and keeping balance. They consist of biogenic crystals of hydroxyapatite and do not contain any living cells. Upon exposure to ionizing radiation, otolith hydroxyapatite accumulates radiation-induced stable CO2- radicals whose amount is proportional to absorbed dose. In electron paramagnetic resonance (EPR) dosimetry, carbonate ions are registered and, hence, the total accumulated dose in the fish otolith can be quantified. Therefore, otoliths can be used as individual fish dosimeters to support radiobiological and radioecological studies. An important aspect of otolith-based EPR dosimetry on fish from contaminated water bodies is the potential presence of bone-seeking 90Sr. Consequently, cumulative absorbed doses measured with EPR in otoliths may reflect the superposition of internal exposure to 90Sr/90Y and external exposure due to radionuclides circulating in soft tissue of the fish as well as due to environmental contamination. The objective of the present study was to develop a method that allows for an assessment of the contribution of 90Sr to the total dose in otolith. The method has been tested using otoliths from seven fish taken from reservoirs located in the Southern Urals contaminated with radionuclides including 90Sr. It has been shown that dose to otoliths is largely determined by 90Sr in the hydroxyapatite. The internal dose component can be calculated using activity concentration-to-dose conversion factors, which vary slightly in the range of 2.0-2.8 × 10-3 Gy year-1 per Bq g-1 depending on fish species and age. Internal doses to fish from water bodies with different levels of 90Sr contamination were calculated in the range from 2 mGy to ~ 200 Gy. External dose contribution was derived for two fish only to be about 100 and 40 Gy. It is concluded that EPR dosimetry on fish otoliths is a promising tool when external exposure prevails or is comparable to internal exposure due to 90Sr.

Microstructural Changes of Human Dentin Tubules after Citric Acid Immersion of Specimens Treated with Different Desensitising Approaches: An SEM Analysis.

PURPOSE: This in-vitro study aimed to evaluate the effectiveness and acid resistance on dentin surfaces following the application of a linear-oscillating device (LOD) with a hydroxyapatite-based polishing fluid, Er:YAG laser or sodium fluoride (NaF) used alone or in combinations for desensitising purposes. MATERIALS AND METHODS: Freshly extracted impacted third molars were used to obtain 120 specimens, all completely immersed in 1% citric acid for 5 min and divided randomly into 6 groups. Group I, with no treatment, served as the control; group II: Er:YAG laser (30 Hz, 60 mJ/pulse, 10 s); group III: NaF gel; group IV: LOD; groups V and VI: the combinations of NaF+Er:YAG and LOD+Er:YAG, respectively, were applied. Following these treatments, the effectiveness of each was evaluated in half of the specimens in each group (n = 10). The other half of the specimens (n = 10) served for acid-resistance testing. All evaluations were made on SEM photomicrographs. RESULTS: The post-treatment tubule diameters and numbers were the lowest with LOD+Er:YAG, followed by NaF+Er:YAG, LOD, Er:YAG and NaF. Paired comparisons revealed LOD+Er:YAG to be the best treatment method (p < 0.05). After 3 h of acid immersion, all treatments revealed significant increases (p < 0.05) in both tubule number and diameter study between post-treatment and post-acid immersion values. The exception was LOD+Er:YAG. LOD+Er:YAG showed the highest resistance to acid challenge, presenting the lowest increase in tubular diameters and numbers followed by NaF+Er:YAG, LOD, Er:YAG and NaF. CONCLUSION: Combined LOD+Er:YAG treatment revealed the highest effectiveness and acid resistance. Further clinical studies are warranted to confirm these in-vitro results.

[Milwaukee shoulder syndrome: A painful swollen shoulder as a result of a rare condition]. / Milwaukee schoudersyndroom.

BACKGROUND: A painful and swollen shoulder has an extensive differential diagnosis, with Milwaukee shoulder syndrome (MSS) being diagnosed infrequently. Analysis of crystals in the synovial fluid is an important diagnostic step in patients with a swollen shoulder. CASE DESCRIPTION: A 69-year-old female presented at the orthopaedic outpatient clinic with pain, limited mobility and swelling of the left shoulder. The diagnosis MSS was made based on the characteristic features on X-ray and MRI combined with the analysis of the synovial fluid, including a positive alizarin-red staining. CONCLUSION: MSS is a rare, destructive, calcium-hydroxyapatite crystal-associated arthropathy. After a typical X-ray, a joint aspiration is preferred to avoid unnecessary expensive radiographic imaging. Alizarin-red staining is a simple, inexpensive, and sensitive test to identify calcium-hydroxyapatite crystals in synovial fluid, and aids in the diagnosis of MSS. This is important in order to adequately inform patients regarding the prognosis of their disease.

Functional role of inorganic trace elements in dentin apatite tissue-part III: Se, F, Ag, and B.

Dentin hydroxyapatite possesses a unique versatile structure which allows it to undergo ionic substitutions. Trace elements play pivotal roles within the oral cavity, especially in dentin apatite tissue. Therefore, it is critical to explore the role of these elements in dentin apatite structure. The roles of other inorganic elements in dentin apatite were discussed in part I (Mg, Sr, Zn, and Fe) and part II (Cu, Mn, Si, and Li) of these series. In the last part of the review series, the role of selenium, fluorine, silver, and boron in the regulation of dentin apatite structure and function was discussed. We evaluated how these elements affect the overall size, morphology, and crystallinity of dentin apatite crystals. Moreover, we investigated the importance of these elements in regulating the solubility of dentin apatite. An electronic search was performed on the role of these trace elements in dentin apatite from January 2010 to January 2022. The concentration of selenium in teeth has been explored only recently, particularly its incorporation into dentin apatite. Silver nanomaterials inhibit the growth of cariogenic microorganisms as well as arrest the degradation of collagen. Fluorine was found to have important roles in dentin remineralization and dentinal tubule occlusion, making it widely used for hydroxyapatite doping. Boron is critical for mineralized tissues like bone, dentin, and enamel, but its exact role in dentin apatite is unknown. Therefore, understanding the impact of these elements on dentin apatite is potentially transformative, as it may help to fill a significant knowledge gap in teeth mechanics.

Functional role of inorganic trace elements in dentin apatite tissue-Part 1: Mg, Sr, Zn, and Fe.

Many essential elements exist in nature with significant influence on dentin and bone apatite tissue. Hydroxyapatite (HAp) is the major inorganic crystalline structure of dentin that provides a site for various physiological functions such as surface layer ion exchange. Decades of apatite research have shown that enamel is a high-substituted crystalline apatite, but recent findings suggest that dentin apatite may play a more important role in regulating ion exchange as well as mineral crystallinity. This article is the first part of a review series on the functional role of inorganic trace elements including magnesium, strontium, zinc, and iron in dentin hydroxyapatite. The morphology, physiology, crystallinity, and solubility of these elements as they get substituted into the HAp lattice are extensively discussed. An electronic search was performed on the role of these elements in dentin apatite from January 2007 to September 2021. The relationship between different elements and their role in the mineral upkeep of dentin apatite was evaluated. Several studies recognized the role of these elements in dentinal apatite composition and its subsequent effects on morphology, crystallinity, and solubility. These elements are of great importance in physiological processes and an essential part of living organisms. Magnesium and strontium stimulate osteoblast activity, while zinc can improve overall bone quality with its antibacterial properties. Iron nanoparticles are also vital in promoting bone tissue growth as they donate or accept electrons in redox reactions. Thus, understanding how these elements impact dentin apatite structure is of great clinical significance.

High temperature CO2 capture of hydroxyapatite extracted from tilapia scales / Captura de CO2 a altas temperaturas, de hidroxiapatitas extraídas de escamas de tilapia / Captura de CO2 a altas temperaturas por hidroxiapatita extraída de escamas de tilápia

Abstract Hydroxyapatite (HAp) was obtained from tilapia scales by two extraction methods: direct calcination and acid-base treatment. The physicochemical characteristics of the obtained HAps were evaluated by thermogravimetric analysis, X-ray fluorescence, X-ray diffraction, scanning electron microscopy, surface area, infrared spectroscopy, and basicity measurement at 298 K by CO2 -pulse titration. Furthermore, the CO2 capture capacity of the solids at high temperature was also determined. Both methods showed the presence of a HAp phase although significant differences in the properties of the solids were found. The HAp obtained by direct calcination, exhibited a lower crystallinity and a greater surface area and basicity than the HAp obtained by the acid-base treatment. These features were correlated with the solid's CO2 capture capacity. In this work, CO2 capture capacity values for HAp yielded by calcination ranged from 2.5 to 3.2 mg CO2 /g captured at 973 K, and for the acid-base treatment-derived HAp, CO2 capture capacity values between 1.2 to 2.5 mg CO2 /g were recorded. These results reveal the potential of HAps extracted from tilapia scales as solids with high CO2 capture capacity, thermal stability, and capture/release cycles reversibility.

Resumen Se obtuvo hidroxiapatita (HAp) de escamas de tilapia por dos métodos de extracción: calcinación directa y tratamiento ácido-base. Las características fisicoquímicas de las HAps obtenidas fueron evaluadas por análisis termogravimétrico, fluorescencia de rayos X, difracción de rayos X, microscopía electrónica de barrido, área superficial, espectroscopia infrarroja y medición de basicidad a 298 K por titulación por pulso de CO2. Adicionalmente, se determinó la capacidad de captura de CO2 de los sólidos a alta temperatura. Ambos métodos mostraron la presencia de una fase de HAp, aunque se encontraron diferencias significativas en las propiedades de los sólidos. La HAp obtenida por calcinación directa exhibió una menor cristalinidad y una mayor área superficial y basicidad que la HAp obtenida con el tratamiento acido-base. Estas características se correlacionaron con la capacidad de captura de CO2 del sólido. En este trabajo, los valores de captura del CO2 con la HAp producidos por calcinación oscilaron entre 2.5 to 3.2 mg CO2/g capturado a 973 K, y con la HAp derivada del tratamiento ácido-base, se registraron valores de captura entre 1.2 to 2.5 mg CO2/g. Estos resultados revelan el potencial de HAps extraídos de escamas de tilapia como sólidos con una alta capacidad de captura de CO2, estabilidad térmica y reversibilidad de los ciclos de captura/liberación.

Resumo A hidroxiapatita (HAp) foi obtida a partir da escama de tilapia usando dois métodos de extração: calcinação direta e tratamento ácido-base. As características físico-químicas das hidroxiapatitas foram avaliadas por análise termogravimétrica, fluorescência de raios-X, difração de raios-X, microscopia eletrônica de varredura, área superficial, espectroscopia de infravermelho e medição de basicidade a 298 K por titulação de pulso de CO2. Além disso, determinou-se a capacidade de captura de CO2 dos sólidos a alta temperatura. Os dois métodos mostraram a presença da fase HAp, no entanto, diferenças significativas foram encontradas nas propriedades dos sólidos, sendo a HAp obtida por calcinação direta a que apresentou menor cristalinidade, maior área superficial e basicidade, características que foram correlacionadas com a capacidade de captura de CO2. Foram encontrados valores entre 2.5 a 3.2 mg CO2/g capturado a 973 K para a HAp obtida por calcinação e, entre 1.2 a 2.5 mg CO2/g para a HAp obtida por tratamento ácido-base. Isto revelou o potencial de HAp's extraídas da escama de tilapia como sólidos com alta capacidade de captura de CO2, estabilidade térmica e reversibilidade na liberação de CO2.

Avaliação histológica e por microscopia eletrônica de varredura da biocerâmica de fosfato de cálcio nano-estruturada micromacro porosa em grânulos em defeito crítico de rádio de coelhos / Histological and nano-structured calcium phosphate bioceramic micro-macro porous granules in critical defect rabbits radius scanning electron microscopy evaluation

Objetivou-se avaliar, histologicamente e por microscopia eletrônica de varredura (MEV), a evolução de defeitos críticos experimentais em rádio de coelhos preenchidos ou não com biocerâmica fosfocálcica nanoestruturada micromacro porosa em grânulos. Utilizaram-se 70 coelhos, Nova Zelândia, adultos jovens, machos, e realizou-se um defeito crítico nos rádios. Os membros constituíram os grupos: GI, biocerâmica lenta, GII, biocerâmica moderada e GIII, controle negativo. Após cada período experimental, os animais foram sacrificados, e os rádios coletados. As avaliações histológicas foram realizadas aos oito, 15, 30, 45, 60, 90 e 120 dias, e as análises de MEV aos 60, 90 e 120 dias. Histologicamente, observou-se processo de reparação óssea mais adiantado nos grupos GI e GII comparando-se ao GIII. Na MEV, constatou-se maior proporção de osso maduro e presença de ósteons secundários nos GI e GII, sendo mais evidente no GII, confirmando os achados histológicos. As cerâmicas promoveram preenchimento completo do defeito, enquanto no grupo controle houve preenchimento no centro do defeito, permanecendo espaços vazios nas laterais. Conclui-se que o emprego das biocerâmicas de absorção lenta e moderada favorece a regeneração óssea completa em defeitos críticos sendo indicadas como substituto ósseo. A maturação óssea ocorre mais precocemente quando se emprega a cerâmica de absorção moderada.(AU)

The objective was to evaluate, through histologic exam and by scanning electron microscopy (SEM), the evolution of experimental critical defects in radio or not filled with nano-structured calcium phosphate micro-macro porous bioceramic granules rabbits. We used 70 rabbits, New Zealand, young adults, males, there was a critical defect in radio. The members were the groups: GI, slow bioceramic, GII, GIII and bioceramic moderate, negative control. After each experimental period, the animals were sacrificed and the radios harvested. Histological evaluations were performed at eight, 15, 30, 45, 60, 90 and 120 days and SEM analyzes at 60, 90 and 120 days. Histologically there was bone healing process earlier in GI and GII compared to GIII. In SEM we observed a higher proportion of mature bone and presence of secondary osteons in GI and GII, being more evident in the GII, confirming the histological findings. Ceramic promoted complete filling of the defect, while the control group was filling in the center of the defect, with empty spaces remaining on the sides. In conclusion, the use of bioceramics, slow and moderate absorption favor complete bone regeneration in critical defects being indicated as a bone substitute. The maturation occurs earlier when employing the ceramic moderate absorption.(AU)

Infrared spectroscopic analysis of staghorn calculi obtained after open renal surgery in a urology unit of Sri Lanka.

The composition of renal stones varies widely among populations. The aim of our study was to determine the composition of staghorn renal stones using Fourier transform infrared (FTIR) spectroscopy in a cohort of Sri Lankan patients. Forty two staghorn calculi removed from kidneys of adult patients during open surgery were analysed. There were 32 men. Nineteen (45%) were calcium oxalate monohydrate (whewellite) stones. Stones containing a mixture of calcium oxalate and calcium hydroxyl phosphate (apatite) were found in 16 (38%). Only 4 (10%) staghorn calculi were coposed of struvite. Three (7%) were uric acid stones. So most staghorn renal stones in Sri Lanka are calcium oxalate. Contrary to the traditional view based on studies done in the western world, only 10% of staghorn calculi removed from patients in Sri Lanka are struvite or infection stones. This could be the reason for kidneys with staghorn calculi in Sri Lanka to retain their function.

Near-Infrared (NIR) Spectroscopy of Synthetic Hydroxyapatites and Human Dental Tissues.

Near-infrared spectroscopy (NIR) was used to analyze synthetic hydroxyapatite calcined at various temperatures, synthetic carbonated hydroxyapatite, and human hard dental tissues (enamel and dentin). The NIR bands of those materials in the combination, first-overtone, and second-overtone spectral regions were assigned and evaluated for structural characterization. They were attributed to adsorbed and structural water, structural hydroxyl (OH) groups and surface P-OH groups. The NIR spectral features were quantitatively discussed in view of proton solid-state magic-angle spinning nuclear magnetic resonance ((1)H MAS NMR) results. We conclude that the NIR spectra of apatites are useful in the structural characterization of synthetic and biogenic apatites.

Oxygen isotope analysis of human bone phosphate evidences weaning age in archaeological populations.

Here we report bone phosphate oxygen (δ(18)Op) values from perinates/neonates and infants (<3.5 years; n = 32); children (4-12 years; n = 12); unsexed juveniles (16-18 years; n = 2); and adult bones (n = 17) from Wharram Percy, North Yorkshire, England, in order to explore the potential of this method to investigate patterns of past breastfeeding and weaning. In prior studies, δ(15)N and δ(13)C analyses of bone collagen have been utilized to explore weaning age in this large and well-studied assemblage, rendering this material highly appropriate for the testing and development of this alternative method targeting the inorganic phase of bone. Data produced reveal (18)O-enrichment in the youngest perinatal/neonatal and infant samples, and an association between age and bone δ(18)Op (and previously-published δ(15)N values), with high values in both these isotope systems likely due to breastfeeding. After the age of 2-3 years, δ(18)Op values are lower, and all children between the ages of 4 and 12, along with the vast majority of sub-adults and adults sampled (aged 16 to >50 years), have δ(18)Op values consistent with the consumption of local modern drinking water. The implications of this study for the reconstruction of weaning practices in archaeological populations are discussed, including variations observed with bone δ(15)Ncoll and δ(18)Op co-analysis and the influence of culturally-modified drinking water and seasonality. The use of this method to explore human mobility and palaeoclimatic conditions are also discussed with reference to the data presented.

[Age and gender changes of apatites from human hard tooth tissues].

Apatites of hard tissues of teeth of persons of different sex and age were studied in detail. It is shown that the crystal structure of apatites depends on changes in the composition of the enamel that happen during a person's life. Limits of the variations of the crystal lattice parameters of the enamel apatites connected with the complicate processes of de- and remineralization have been determined. On the basis of the identified correlations between chemical composition, crystal lattice parameters and age of patients, the complicated interrelated isomorphic replacements occurring in the crystal structure of apatites of hard tooth tissues during aging were analysed.

Characterization and analyses of acid-extractable and leached trace elements in dental cements.

AIMS: Determination of the elemental constitution and investigation of the total and leachable arsenic, chromium and lead in Portland cement, pure tricalcium silicate, Biodentine, Bioaggregate and mineral trioxide aggregate (MTA) Angelus. METHODOLOGY: The chemical composition of Portland cement, MTA Angelus, tricalcium silicate cement, Biodentine and Bioaggregate was determined using X-ray fluorescence (XRF). Measurements of arsenic, lead and chromium were taken with inductively coupled plasma-mass spectrometry (ICP-MS), following acid digestion on the hydrated material and on leachates of cements soaked in Hank's balanced salt solution (HBSS). RESULTS: All the cements investigated had a similar oxide composition with the main oxide being calcium and silicon oxide. Both the Portland cement and MTA Angelus had an additional aluminium oxide. The dental cements included a radiopacifying material. All the materials tested had higher acid-extractable arsenic content than the level set by ISO 9917-1 (2007) and an acceptable level of lead. Regardless these high levels of trace elements present in the materials, the leaching in HBSS was minimal for all the dental material tested in contrast to the high levels displayed by Portland cement. CONCLUSIONS: Dental materials based on tricalcium silicate cement and MTA Angelus release minimal quantities of trace elements when in contact with simulated body fluids. The results of acid extraction could be affected by nonspecific matrix effects by the cement.

Formation of caries-like lesions in vitro on the root surfaces of human teeth in solutions simulating plaque fluid.

Lesion formation on root surfaces of human posterior teeth was studied in acetate/lactate buffers with a background electrolyte composition based on plaque fluid analyses. Lesion depth after 28 days at 37 degrees C was measured in relation to: the presence or absence of cementum; the concentration of undissociated buffer; the presence or absence of magnesium ions at plaque fluid concentration. Each factor was evaluated at several values of -log(ion activity product for hydroxyapatite): pI(HA). Solutions were formulated to minimize variation in pH, which varied by < or =0.03 for a given comparison (individual pI(HA)) and by 0.42-0.82 over the range of pI(HA) within experiments. Lesions on surfaces from which cementum had been ground were significantly deeper than on intact surfaces, but this is considered to be due to subsurface mechanical damage and not to a solubility difference. Neither the concentration of undissociated buffer nor the presence of magnesium ions significantly affected lesion depth. Lesion depth was strongly influenced by the correlated variations in pI(HA) and pH. At pI(HA) 54 and 55, only extremely shallow lesions formed. From pI(HA) 56, lesion depth increased with increasing pI(HA). The results confirm that the solubility of the mineral of root tissues is higher than that of hydroxyapatite, but indicate that it is probably lower than suggested by Hoppenbrouwers et al. [Arch Oral Biol 1987;32:319-322]. For calcium concentrations of 3-12 mM, the critical pH for root tissue mineral was calculated as 5.22-5.66 assuming solubility equivalent to pI(HA) 54 and 5.08-5.51 assuming pI(HA) 55.

A system of calibrating microtomography for use in caries research.

Desktop microcomputed tomography (micro-CT) offers a non-invasive 3-dimensional analysis of structures and their physical properties. To date, the use of micro-CT has mostly involved qualitative observations, with the extent of quantitative analysis relying on automated internal calibration by the micro-CT control software. However, the value of such calibration is limited by machine drift. For an accurate quantitative use of micro-CT, it is recognized that external means of calibration are needed. A novel system of calibration standards, also known as 'phantoms', is presented. A range of low mineral concentration phantoms involving triethylene glycol dimethacrylate/glycerolate dimethacrylate resin mixed with commercial pure hydroxyapatite (HAP), from 0.07 to 1.05 g/cm(3), was fabricated. Sintered HAP was impregnated with the same resin, producing phantoms with medium-level mineral concentrations up to 1.90 g/cm(3). These phantoms were easy to create, proved accurate and stable with repeated use, and were found to mimic the composite nature of dental enamel and dentine structures under investigation.

[Role of enamel matrix proteins in inducing biomimetic mineralization of the enamel: a study with quartz crystal microbalance technique].

OBJECTIVE: To investigate the adsorption behavior of enamel matrix proteins (EMPs) on the enamel surface and study their effect on biomineralization of enamel using quartz crystal microbalance (QCM) technique. METHODS AND RESULTS: The EMPs were adsorbed on the enamel surface to form a protein film, which was soaked in simulated body fluid solutions. After 30 days of biomimetic mineralization, the hydroxyapatite nucleation, growth and aggregation occurred with hydroxyapatite crystal formation on the enamel surface. CONCLUSION: The EMPs play a key role in regulating enamel mineralization.

Osseous alterations at the interface of hydrogel expanders and underlying bone.

INTRODUCTION: In plastic and reconstructive surgery, self-activating hydrogel expanders are used to augment soft-tissue space. The purpose of this study was to investigate the morphological response of underlying bone to the constant pressure exerted by a hydrogel expander. METHODS: Eighteen Lewis rats were randomly divided into three groups. In group 1, a hydrogel expander was placed subperiosteally directly onto the calvaria of the rats. In group 2, the expander and the underlying bone were separated by a polydioxanone (PDS) foil. Group 3 animals served as controls. Before and 14 days after the insertion of the expanders, micro-computed tomography (CT) images were obtained and fused. We analysed hydroxyapatite density beneath and at the periphery of the expander and performed a histomorphometric bone analysis. RESULTS: Whereas there were no significant differences (p<0.05) (groups 1 and 2) in bone density at the periphery of the expanders between the study groups, a significant decrease in hydroxyapatite density beneath the expanders was observed in those animals in which the devices were placed directly onto the calvaria (group 1). Whereas bone thickness was unaffected at the periphery of the expanders in all groups, it was significantly decreased beneath the expanders in all implanted animals. A morphological examination revealed resorption lacunae with a diameter of 218.4+/-56 mICROm in those rats in which the expanders had been placed directly onto the calvaria. CONCLUSION: This study shows the direct influence of hydrogel expanders on underlying bone. Whereas bone resorption and connective tissue formation also occur underneath hydrogel expanders, these effects can be avoided if the expander and the underlying bone are separated by PDS foil. The key to success is to ensure the appropriate placement of expanders and thus to avoid bone resorption.

Phosphate dynamics in an urban sewer: a case study of Nancy, France.

The nature of phosphate phases present in suspended matter, biofilm, and sediment of Greater Nancy sewer system was investigated over a period of two years. The phosphate speciation was determined by two approaches: a direct identification of phosphorus mineral phases was conducted by Transmission Electron Microscopy (TEM) coupled with energy-dispersive X-ray spectroscopy (EDXS), whereas a chemical extraction of samples provided an estimate of phosphorus pools defined by the fractionation scheme. Quantitative analysis of 1340 individual particles by TEM-EDXS allowed to draw a picture of phosphate species distributions along the sewer system and over time. Amorphous Ca-phosphates (brushite, whitlockite, octacalcium phosphate, Mg-brushite, hydroxyapatite and carbapatite) were ubiquitous although brushite dominated upstream, and octacalcium phosphate and apatite prevailed downstream and in sediments. Al-Ca-phosphate minerals such as foggite, bearthite, gatumbaite, and crandallite appeared downstream and in biofilms. Ca-phosphate phase assemblages in the different locations of the sewer system were dependent on phase transformations from brushite to hydroxyapatite that were shown to be kinetically driven. The restriction of Al-Ca-phosphates to downstream of the sewer system was most probably related to the lower pHs measured at these sites. The pH dependency was confirmed by stability calculations. Chemical extractions were not reliable. TEM examination of extraction residues revealed the presence of neoformed Al-Ca-phosphate species that invalidated the fractionation scheme. Nonetheless, it confirmed that phosphate phases may undergo significant geochemical changes over a short time scale.

In vitro study of matrix surface properties of porous granulated calcium phosphate ceramic materials made in Russia.

We performed in vitro screening of monophasic (hydroxyapatite, beta-tricalcium phosphate, carbonate-substituted hydroxyapatite with 0.59 and 5.9 wt% substitution with CO(3)(2-)) and biphasic (hydroxyapatite-tricalcium phosphate with various percentage of the components 80/20, 60/40, 20/80, silicon-substituted hydroxyapatite with 0.79 wt% SiO(2)) porous granulated ceramics composed of calcium phosphate powders synthesized by methods of heterophasic interaction of reagents and precipitation from aqueous solutions using MTT test and cultured human fibroblasts. Acute toxicity of materials (24-h incubation with cell culture) and matrix properties (3, 5, 7, 14, 18, 21, 28 days in culture) were evaluated. We selected a batch of materials obtained by precipitation from aqueous solutions, which were non-toxic and were characterized by good matrix properties (for cells). Biphasic ceramics with hydroxyapatite-tricalcium phosphate ratio of 80/20 exhibited best characteristics, and ceramics on the basis of silicon-substituted hydroxyapatite showed moderate characteristics.