Elucidating the Mechanism of Efficient Eu(III) and Yb(III) Sensitisation from a Re(I) Tetrazolato Triangular Assembly.

The reaction of Re(CO)5Br with deprotonated 1H-(5-(2,2':6',2''-terpyridine)pyrid-2-yl)tetrazole yields a triangular assembly formed by tricarbonyl Re(I) vertices. Photophysical measurements reveal blue-green emission with a maximum at 520 nm, 32 % quantum yield, and 2430 ns long-lived excited state decay lifetime in deaerated dichloromethane solution. Coordination of lanthanoid ions to the terpyridine units red-shifts the emission to 570 nm and also reveals efficient (90 %) and fast sensitisation of both Eu(III) and Yb(III) at room temperature, with a similar rate constant kET on the order of 107 s-1. Efficient sensitisation of Eu(III) from Re(I) is unprecedented, especially when considering the close proximity in energy between the donor and acceptor excited states. On the other hand, comparative measurements at 77 K reveal that energy transfer to Yb(III) is two orders of magnitude slower than that to Eu(III). A two-step mechanism of sensitisation is therefore proposed, whereby the rate-determining step is a thermally activated energy transfer step between the Re(I) centre and the terpyridine functionality, followed by rapid energy transfer to the respective Ln(III) excited states. At 77 K, the direct Re(I) to Eu(III) energy transfer seems to proceed via a ligand-mediated superexchange Dexter-type mechanism.

Alkali Silicates Codoped with NIR-Emitting RE (Nd3+ and Yb3+) Ions for Thermometry Applications.

In the present study, the synthesis of BaSrSiO4 co-doped Yb3+ and Nd3+ nanophosphors (NPs) was successfully achieved through the conventional sol-gel method, as confirmed by X-ray diffraction and SEM analysis, verifying the formation of pure NPs. The FTIR and Raman spectra analysis confirm the formation of silicates, as different modes and vibrations of Si-O and Si-O-Si were seen at 800-1000 cm-1. The energy transfer (ET) mechanism between Nd3+ and Yb3+ ions was seen as the emission spectra showed a rise in intensity of one over another. PLE emission spectra showed transitions at 2F7/2-2F5/2 for Yb3+ and from 4F3/2 to (4I9/2, 4I11/2, and 4I13/2) for Nd3+ when excited at 785 nm. All the samples record low activation energy, which shows that the rate of reaction will be higher in all the samples, and it will be highest for 1 mol% Nd3+ and 1 mol% Yb3+. An increasing value of τ was seen with increasing Yb3+ concentration, which confirms the increase in the population of trap centers. The positron annihilation lifetime (PAL) curve showed that 1 mol% Yb3+ and 2 mol Nd3+ have single vacancies or shallower positron traps, whereas 3 mol% Yb3+ and 2 mol% Nd3+ have larger defects like surface oxygen vacancy clusters. The other two samples have balance vacancies, which makes them best for thermometry applications. The fluorescence intensity ratio (FIR) was calculated to get sensitivity for thermometry application. 2.13% K-1 sensitivity achieved at 303-333 K temperature.

Similarities and Differences in Benzene Reduction with Ca, Sr, Yb and Sm: Strong Evidence for Tetra-Anionic Benzene.

Inverse sandwich complexes of Yb and Sm stabilized by a bulky ß-diketiminate (BDI) ligand have been prepared: (BDI)Ln(η6,η6-C6H6)Ln(BDI); Ln=lanthanide. Coordinated benzene ligands can be neutral, di-anionic or, often controversially discussed, even tetra-anionic. The formal charge on benzene is correlated to assignment of the metal oxidation state which generally poses a problem. Herein, we take advantage of the structural similarities found when comparing CaII with YbII, and SrII with SmII complexes. In this work, we found an excellent overlap of the Ca/Yb inverse sandwich structures but a striking difference for the Sr/Sm pair. The much shorter Sm-N and Sm-C6H6 distances are strong evidence for a SmIII-benzene-4-SmIII assignment. This was further supported by NMR spectroscopy, magnetic susceptibility, reactivity and comprehensive computational investigation.

Yb2+-Doped Silicate Glasses as Optical Sensor Materials for Cryogenic Thermometry.

Optical sensors constitute attractive alternatives to resistive probes for the sensing and monitoring of temperature (T). In this work, we investigated, in the range from 2 to 300 K, the thermal behavior of Yb2+ ion photoluminescence (PL) in glass hosts for cryogenic thermometry. To that end, two kinds of Yb2+-doped preforms, with aluminosilicate and aluminophosphosilicate core glasses, were made using the modified chemical vapor deposition (MCVD) technique. The obtained preforms were then elongated, at about 2000 °C, to canes with an Yb2+-doped core of about 500 µm. Under UV excitation and independently of the core composition, all samples of preforms and their corresponding canes presented a wide visible emission band attributed to Yb2+ ions. Furthermore, PL kinetics measurements, recorded at two emission wavelengths (502 and 582 nm) under 355 nm pulsed excitation, showed an increase, at very low T, followed by a decrease in lifetime until room temperature (RT). A modified two-level model was proposed to interpret such a decay time dependence versus T. Based on the fit of lifetime data with this model, the absolute (Sa) and relative (Sr) sensitivities were determined for each sample. For both the preform and its corresponding cane, the aluminophosphosilicate glass composition featured the highest performances in the cryogenic domain, with values exceeding 28.3 µsK-1 and 94.4% K-1 at 30 K for Sa and Sr, respectively. The aluminophosphosilicate preform also exhibited the wider T operating range of 10-300 K. Our results show that Yb2+-doped silicate glasses are promising sensing materials for optical thermometry applications in the cryogenic domain.

Spectroscopic analysis of N-intrashell transitions in Rb-like to Ni-like Yb ions.

Extreme ultraviolet spectra of highly-charged ytterbium ions produced in an electron beam ion trap at the National Institute of Standards and Technology were observed with a flat-field grazing incidence spectrometer in the wavelength region of about 4 nm-20 nm. The measured spectra were interpreted through detailed analysis by collisional-radiative modeling of the non-Maxwellian EBIT plasma. Seventy-nine new spectral lines due to intrashell (Δn = 0, n = 4) electric-dipole, magnetic-dipole, and electric-quadrupole transitions were identified in Rb-like Yb33+ through Ni-like Yb42+ ions. The effects of strong configuration interaction within the n = 4 complex on the measured spectra are discussed for a number of ionization stages.

Investigating Laser Ablation Process Parameters for the Fabrication of Customized Microneedle Arrays for Therapeutic Applications.

Microneedles are an innovation in the field of medicine that have the potential to revolutionize drug delivery, diagnostics, and cosmetic treatments. This innovation provides a minimally invasive means to deliver drugs, vaccines, and other therapeutic substances into the skin. This research investigates the design and manufacture of customized microneedle arrays using laser ablation. Laser ablation was performed using an ytterbium laser on a polymethyl methacrylate (PMMA) substrate to create a mold for casting polydimethylsiloxane (PDMS) microneedles. An experimental design was conducted to evaluate the effect of process parameters including laser pulse power, pulse width, pulse repetition, interval between pulses, and laser profile on the desired geometry of the microneedles. The analysis of variance (ANOVA) model showed that lasing interval, laser power, and pulse width had the highest influence on the output metrics (diameter and height) of the microneedle. The microneedle dimensions showed an increase with higher pulse width and vice versa with an increase in pulse interval. A response surface model indicated that the laser pulse width and interval (independent variables) significantly affect the response diameter and height (dependent variable). A predictive model was generated to predict the microneedle topology and aspect ratio varying from 0.8 to 1.5 based on the variation in critical input process parameters. This research lays the foundation for the design and fabrication of customized microneedles based on variations in specific input parameters for therapeutic applications in dermal sensors, drug delivery, and vaccine delivery.

Theoretical investigations on the laser isotope separation of 175Yb for medical applications.

The possibility of laser isotope separation of 175Yb from irradiated natural Yb has been investigated. The optimum process parameters such as powers and bandwidths of the lasers, Doppler broadening and the number density of the atoms have been derived through density matrix calculations. It has been shown that it is possible to produce 175Yb (>42% enriched) at a production rate of 62 µg/hour (or 1.5 mg/day). This corresponds to the production rate of 1350 patient doses (of 7.4 GBq each) per day. The radionuclidic purity of the isotopic mixture is expected to be 99.9999%. The method is highly suitable for the countries having only low-flux nuclear reactors.

A re-activation model for 169Yb intensity modulated brachytherapy sources accounting for spatiotemporal isotopic composition.

BACKGROUND: Intensity modulated brachytherapy based on partially shielded intracavitary and interstitial applicators is possible with a cost-effective 169Yb production method. 169Yb is a traditionally expensive isotope suitable for this purpose, with an average γ-ray energy of 93 keV. Re-activating a single 169Yb source multiple times in a nuclear reactor between clinical uses was shown to theoretically reduce cost by approximately 75% relative to conventional single-activation sources. With re-activation, substantial spatiotemporal variation in isotopic source composition is expected between activations via 168Yb burnup and 169Yb decay, resulting in time dependent neutron transmission, precursor usage, and reactor time needed per re-activation. PURPOSE: To introduce a generalized model of radioactive source production that accounts for spatiotemporal variation in isotopic source composition to improve the efficiency estimate of the 169Yb production process, with and without re-activation. METHODS AND MATERIALS: A time-dependent thermal neutron transport, isotope transmutation, and decay model was developed. Thermal neutron flux within partitioned sub-volumes of a cylindrical active source was calculated by raytracing through the spatiotemporal dependent isotopic composition throughout the source, accounting for thermal neutron attenuation along each ray. The model was benchmarked, generalized, and applied to a variety of active source dimensions with radii ranging from 0.4 to 1.0 mm, lengths from 2.5 to 10.5 mm, and volumes from 0.31 to 7.85 mm3, at thermal neutron fluxes from 1 × 1014 to 1 × 1015 n cm-2 s-1. The 168Yb-Yb2O3 density was 8.5 g cm-3 with 82% 168Yb-enrichment. As an example, a reference re-activatable 169Yb active source (RRS) constructed of 82%-enriched 168Yb-Yb2O3 precursor was modeled, with 0.6 mm diameter, 10.5 mm length, 3 mm3 volume, 8.5 g cm-3 density, and a thermal neutron activation flux of 4 × 1014 neutrons cm-2 s-1. RESULTS: The average clinical 169Yb activity for a 0.99 versus 0.31 mm3 source dropped from 20.1 to 7.5 Ci for a 4 × 1014 n cm-2 s-1 activation flux and from 20.9 to 8.7 Ci for a 1 × 1015 n cm-2 s-1 activation flux. For thermal neutron fluxes ≥2 × 1014 n cm-2 s-1, total precursor and reactor time per clinic-year were maximized at a source volume of 0.99 mm3 and reached a near minimum at 3 mm3. When the spatiotemporal isotopic composition effect was accounted for, average thermal neutron transmission increased over RRS lifetime from 23.6% to 55.9%. A 28% reduction (42.5 days to 30.6 days) in the reactor time needed per clinic-year for the RRS is predicted relative to a model that does not account for spatiotemporal isotopic composition effects. CONCLUSIONS: Accounting for spatiotemporal isotopic composition effects within the RRS results in a 28% reduction in the reactor time per clinic-year relative to the case in which such changes are not accounted for. Smaller volume sources had a disadvantage in that average clinical 169Yb activity decreased substantially below 20 Ci for source volumes under 1 mm3. Increasing source volume above 3 mm3 adds little value in precursor and reactor time savings and has a geometric disadvantage.

Novel Bidirectional Output Ytterbium-Doped High Power Fiber Lasers: From Continuous to Quasi-Continuous.

Traditional ytterbium-doped high-power fiber lasers generally use a unidirectional output structure. To reduce the cost and improve the efficiency of the fiber laser, we propose a bidirectional output fiber laser (BOFL). The BOFL has many advantages over that of the traditional unidirectional output fiber laser (UOFL) and has a wide application in the industrial field. In theory, the model of the BOFL is established, and a comparison of the nonlinear effect in the traditional UOFL and the BOFL is studied. Experimentally, high-power continuous wave (CW) and quasi-continuous wave (QCW) BOFLs are demonstrated. In the continuous laser, we first combine the BOFL with the oscillating amplifying integrated structure, and a near-single-mode bidirectional 2 × 4 kW output with a total power of above 8 kW is demonstrated. Then, with the simple BOFL, a CW bidirectional 2 × 5 kW output with a total power of above 10 kW is demonstrated. By means of pump source modulation, a QCW BOFL is developed, and the output of a near-single mode QCW laser with a peak output of 2 × 4.5 kW with a total peak power of more than 9 kW is realized. Both CW and QCW output BOFL are the highest powers reported at present.

Radiopacity and physical properties evaluation of infiltrants with Barium and Ytterbium addition

Abstract Radiopaque properties in the infiltrant should be interesting for clinicians to feel more confident to indicate this treatment. Thus, the aim of this study was to evaluate the effect of the incorporation of barium and ytterbium particles on the physical properties of resin infiltrants. Groups were divided according to the addition of ytterbium oxide (Y) alone (30 or 40%) or Y with barium (YB) (15/15% or 20/20% respectively) in the Icon commercial infiltrant and in the experimental infiltrant base. Digital radiography (n=5), Microradiography (n=5), Microtomography (n=3), degree of conversion (n=5), water sorption (n=16), solubility (n=16), contact angle (n=16), flexural strength (n=16), elastic modulus (n=16) and Energy dispersive X-ray Spectroscopy (n=10) were performed. Analyses were performed using the R program, with a significance level of 5%, and microradiography and Microtomography analyses were evaluated qualitatively. In groups with 30 or 40% of ytterbium, radiopacity was higher or equal to enamel. Microradiography and Microtomography appear to have more radiopacity in groups with 40% (Y). Among the groups with no particle addition, those of the experimental infiltrant presented a higher degree of conversion than those of Icon®. In most groups, there was solubility below the ISO-recommended levels. The addition of particles resulted in higher viscosity. Groups with Icon had higher flexural strength and elastic modulus than groups with experimental infiltrant. The addition of 40% (Y) improved polymerization, had low solubility, and had greater radiopacity than enamel, however negatively affected the viscosity increasing then. Experimental groups with the base showed a higher water sorption than Icon groups.

Resumo O objetivo desse estudo foi avaliar o efeito da incorporação de partículas de Bário e Itérbio nas propriedades físicas de infiltrantes resinosos. Os grupos foram divididos de acordo com a adição de Itérbio puro (30 ou 40%) ou Itérbio com Bário (15/15% ou 20/20% respectivamente) no infiltrante comercial Icon e no Infiltrante experimental base. Foram realizados os testes de: radiografia digital (n=5), microradiografia Transversa (n=5), microtomografia (n=3), grau de conversão (n=5), sorção (n=16), solubilidade (n=16), ângulo de contato (n=16), resistência flexural (n=16), modulo de elasticidade (n=16) e Espectroscopia por energia dispersiva (n=10). As análises foram realizadas utilizando o programa R, com nível de significância de 5%, e os testes de microradiografia e microtomografia foram analisados qualitativamente. Nos grupos com 30 ou 40% de Itérbio, a radiopacidade foi maior ou igual ao esmalte dentário. Na microradiografia e microtomografia parece ter maior radiopacidade nos grupos com 40% de itérbio. Dentre os grupos sem adição de partículas, os do infiltrante experimental apresentaram maior grau de conversão do que os do Icon e o grupo controle experimental e com 40% de itérbio apresentaram os melhores resultados. Na maioria dos grupos, a solubilidade foi abaixo dos níveis recomendados pela ISO. A adição de particulas resultou em maior viscosidade. Os grupos com Icon apresentaram maior resistência flexural e modulo de elasticidade do que os grupos com infiltrante experimental e a quantidade de partícula aumentou a resistência e o módulo de elasticidade. A adição de 40% de itérbio melhorou a polimerização, apresentou baixa solubilidade e maior radiopacidade do que o esmalte, porém afetou negativamente a viscosidade, aumentando-a.

The effect of adding ytterbium trifluoride on the radiopacity, compressive strength, setting time and bioactivity of biodentine: an in vitro study / Efeito da adição de trifluoreto de itérbio na radiopacidade, resistência à compressão, tempo de presa e bioatividade da biodentina: estudo in vitro

Objective: This study aimed to evaluate the radiopacity, compressive strength, setting time and bioactivity of Biodentine after modification with Ytterbium Tri-Fluoride (YbF3) in three different concentrations. Material and Methods: Radiopacity was determined using the equivalence in millimeters of aluminum (mm Al) from digital radiographs. Compressive strength was evaluated using a universal testing machine. The initial and final setting times were evaluated using Gillmore needle. The bioactive potential was evaluated using the environmental scanning electron microscope (ESEM) connected with Energy Dispersive X-ray analysis (EDX) and X-ray Diffractometer (XRD) at three different time intervals. pH was measured using a pH-meter. Data were analyzed using one-way ANOVA followed by Tukey's post hoc tests (P≤ 0.05). Results: Radiopacity of Biodentine with 2.5%, 5% and 7.5% YbF3 was significantly higher than unmodified Biodentine (P ≤ 0.05). Unmodified Biodentine showed the highest mean compressive strength values compared to all other groups (p≤ 0.05). The addition of YbF3 to Biodentine has extended the final setting time except for the 2.5% YbF3 group that showed no significant difference compared to the control. All groups showed an alkaline pH at 28 days, ESEM coupled with EDX analysis showed evidence of dense globules of calcium phosphate on the surface indicating enhancement of bioactivity. Conclusion: 2.5% YbF3 can be a promising radiopacifying agent to Biodentine with improvement in radiopacity, bioactive potential and maintaining the setting time and compressive strength at acceptable level as indicated by the ISO standards (AU)

Objetivo: O estudo buscou avaliar a radiopacidade, resistência à compressão, tempo de presa e bioatividade da Biodentina modificada por Trifluoreto de itérbio (YbF3). Materiais e Métodos: YbF3 foi incorporado ao pó de Biodentina e dividido em 4 grupos (X0, X1, X2 e X3) de acordo com a concentração de YbF3; 0%, 2.5%, 5% e 7.5% do peso, respectivamente. Os espécimes foram preparados para cada experimento com um total de 40 espécimes para cada teste (n=10 por grupo). A radiopacidade foi determinada através do uso equivalente em milímetros de alumínio. A resistência a compressão foi avaliada através do uso de uma máquina de teste universal. O tempo inicial e final foi avaliado através de uma agulha de Gillmore. O potencial bioativo foi avaliado através do Microscópio Eletrônico de Varredura (ESEM), conectado com a análise de espectroscopia de raios X por energia dispersiva (EDX) e difração de raio X (DRX). O pH foi mensurado através do uso de um pHmetro. Os dados foram analisados pelo ANOVA seguido do Test Tukey. Resultados: A radiopacidade nos grupos X1, X2 e X3 foi significantemente maior do que no grupo X0. O grupo X0 mostrou a maior resistência à compressão comparado com os outros grupos. A adição de YbF3 a Biodentina excedeu o tempo final exceto pelo grupo X1, que não apresentou diferença estatística significante quando comparado com o grupo X0. Todos os grupos apresentaram um pH alcalino com 28 dias. ESEM com análise EDX mostrou evidência de densos glóbulos de fosfato de cálcio na superfície, indicando uma melhora na bioatividade. Conclusão: 2.5% YbF3 é um promissor radiopacificador para Biodentina, que aumentou a radiopacidade e potencial bioativo enquanto manteve o tempo definido e a resistência à compressão em níveis aceitáveis como indica a norma ISO.(AU)

Ytterbium oxide as radiopacifier of calcium silicate-based cements. physicochemical and biological properties

Abstract This study evaluated physicochemical properties, cytotoxicity and bioactivity of MTA Angelus (MTA), calcium silicate-based cement (CSC) and CSC with 30% Ytterbium oxide (CSC/Yb2O3). Setting time was evaluated using Gilmore needles. Compressive strength was evaluated in a mechanical machine. Radiopacity was evaluated using radiographs of materials and an aluminum scale. Solubility was evaluated after immersion in water. Cell viability was evaluated by means of MTT assay and neutral red staining, and the mineralization activity by using alkaline phosphatase activity and Alizarin Red staining. The data were submitted to ANOVA, Tukey and Bonferroni tests (5% significance). The bioactive potential was evaluated by scanning electron microscopy. The materials presented similar setting time. MTA showed the lowest compressive strength. MTA and CSC/Yb2O3 presented similar radiopacity. CSC/Yb2O3 showed low solubility. Saos-2 cell viability tests showed no cytotoxic effect, except to 1:1 dilution in NR assay which had lower cell viability when compared to the control. ALP at 1 and 7 days was similar to the control. MTA and CSC had greater ALP activity at 3 days when compared to control. All the materials present higher mineralized nodules when compared with the control. SEM analysis showed structures suggesting the presence of calcium phosphate on the surface of materials demonstrating bioactivity. Ytterbium oxide proved to be a properly radiopacifying agent for calcium silicate-based cement since it did not affected the physicochemical and biological properties besides preserving the bioactive potential of this material.

Resumo Este estudo avaliou as propriedades físico-químicas, citotoxicidade e bioatividade do MTA Angelus (MTA), cimento à base de silicato de cálcio (CSC) e CSC com 30% de óxido de itérbio (CSC/Yb2O3). O tempo de presa foi avaliado usando agulhas Gilmore. A resistência à compressão foi avaliada em uma máquina mecânica. A radiopacidade foi avaliada utilizando radiografias dos materiais e uma escala de alumínio. A solubilidade foi avaliada após imersão em água. A viabilidade celular foi avaliada por meio do ensaio MTT e coloração de vermelho neutro (NR), e a atividade de mineralização por meio da atividade da fosfatase alcalina e a coloração com Vermelho de Alizarina. Os dados foram submetidos aos testes ANOVA, Tukey e Bonferroni (5% de significância). O potencial bioativo foi avaliado por microscopia eletrônica de varredura. Os materiais apresentaram tempo de presa semelhante. O MTA mostrou menor resistência à compressão. MTA e CSC/Yb2O3 apresentaram radiopacidade semelhante. CSC/Yb2O3 apresentou menores valores de solubilidade. A viabilidade celular realizada pelos ensaios de MTT e NR não revelaram efeitos ctotóxicos em todas as diluições, exceto na diluição 1:1 no NR, o qual mostrou baixa viabilidade celular (p<0.05) em todos materiais testados quando comparado ao controle. A atividade de ALP em 1 e 7 dias foi similar ao controle (p>0.05). MTA e CSC tiveram significante aumento na atividade de ALP aos 3 dias quando comarados ao controle (p>0.05). Todos os materiais apresentaram grande produção de nódulos mineralizados quando comparados ao controle (P<0.05). A análise da SEM mostrou estruturas que sugerem a presença de depósitos de fosfato de cálcio na superfície dos materiais demonstrando bioatividade. O Yb2O3 mostrou ser um agente radiopacificador adequado em cimentos à base de silicato de cálcio uma vez que não afetou as propriedades físico-químicas e biológicas e ainda preservou o potencial bioativo desse material.

Microscopic description of low-lying properties in 168≤A≤170 Yb nuclei by the pseudo-SU(3) shell model / Descripción microscópica de las propiedades de baja energía de los núcleos 168≤A≤170 Yb usando el modelo pseudo-SU(3)

Abstract The rare-earth nuclei have well-known collective properties. The theoretical description of these nuclei represents a challenge to nuclear models, due to the enormous dimensions of the valence space, making the problem unmanageable. This leads us to use symmetry-based models, where it is possible to calculate in a free-truncation environment. In this work we present results for the energy spectrum and the electromagnetic properties in even-even Yb isotopes using the pseudo-SU(3) shell model. The model considers a Nilsson Hamiltonian that additionally includes the quadrupole-quadrupole and pairing interactions, systematically parameterized. The results show that the model considered is a powerful theoretical tool, allowing us to describe the normal parity sector of deformed rare earth nuclei.

Resumen Las propiedades colectivas de los núcleos de las tierras raras están muy bien determinadas. La descripción teórica de estos núcleos representa un desafío para cualquier modelo nuclear debido a las dimensiones excesivas del espacio de valencia, lo que vuelve el problema inmanejable. Esto nos lleva a emplear modelos basados en simetrías, donde es posible realizar cálculos sin truncamiento del espacio. En este trabajo se presentan resultados para el espectro energético y las propiedades electromagnéticas en isótopos para-par de iterbio, utilizando el modelo de capas pseudo-SU(3). El modelo considera el hamiltoniano de Nilsson, al que adicionalmente se le han incluido las interacciones cuadrupolo-cuadrupolo y de apareamiento, parametrizadas de forma sistemática. El resultado muestra que el modelo utilizado es una herramienta poderosa que permite describir el sector de paridad normal del espectro de núcleos deformados de las tierras raras.

Estudo comparativo da osseointegração de implantes manufaturados em Ti-cp ou Ti6Al4V com ou sem superfície modificada por ablação a laser: caracterização topográfica, análises biomecânica, histólogica e imunoistoquímica / Comparative study of osseointegration of implants manufactured in cp-Ti or Ti6Al4V with or without modified surface by laser beam: topographic characterization, biomechanical, histological and immunohistochemical analyzes

A proposição do trabalho foi avaliar o comportamento biológico e mecânico ao tecido ósseo periimplantar em implantes manufaturados em Ti-cp com superfícies usinada (CPMS) e modificada por LASER (CPLS) e implantes manufaturados em Ti6Al4V com superfícies usinada (ALLOYMS) e modificada por LASER (ALLOYLS). As superfícies foram analisadas por meio da microscopia eletrônica de varredura acoplado a espectroscopia por energia dispersiva de raios X (MEV-EDX) previamente a cirurgia experimental. Noventa e seis (2x4mm) implantes foram instalados em leitos cirúrgicos fresados nas tíbias direita e esquerda de 48 ratos Wistar machos, sendo um implante de cada material (metal) ou superfície instalado em cada tíbia. Análise biomecânica foi realizada por meio do torque de remoção dos implantes em todos os grupos nos períodos de 14, 21 e 42 dias pós-operatório e as tíbias foram seccionadas e processadas para análise histológica e imunoistoquímica. Posteriormente, foi realizada MEV-EDX dos implantes removidos por torque reverso em todos os períodos de análises. Os dados obtidos na análise biomecânica foram submetidos à análise estatística (p< 0,05). MEV-EDX antes da instalação dos implantes apresentou diferença entre as superfícies usinadas e modificadas por LASER, independente do metal do implante. O torque de remoção de ALLOYLS foi estatisticamente superior a CPLS, CPMS e ALLOYMS em 14 e 21 dias (p < 0,05), bem como CPLS foi estatisticamente superior a CPMS e ALLOYMS. Aos 42 dias CPLS e ALLOYLS apresentaram diferenças estatística quando comparados com CPMS e ALLOYMS (p< 0,05), porém não foi observada diferença entre CPLS e ALLOYLS (p = 0,07). O MEV-EDX dos implantes removidos por contra-torque evidenciou o recobrimento ósseo total das superfícies de CPLS e ALLOYLS, independe do período analisado e um aumento gradual de recobrimento ósseo nas superfícies de CPMS e ALLOYMS nos períodos de 14, 21 e 42 dias respectivamente, sendo que o CPLS aos 42 dias apresentou característica de tecido ósseo mais maturo. Na análise histológica qualitativa observa-se um tecido ósseo mais maturo, sugerindo aceleração do processo de reparo ósseo nos grupos CPLS e ALLOYLS. Para análise imunoistoquímica observou-se uma maior expressão de OPN (osteopontina) para os grupos ALLOYLS 14 e 21 dias pós-operatório, surgindo de maior ativação celular. Os implantes com modificação de superfície por ablação a LASER, independente do material manufaturado, proporcionaram importantes modificações físico-químicas na superfície, permitindo melhor embricamento mecânico com o tecido ósseo e aceleração do processo de osseointegração quando comparados com implantes com superfície usinada(AU)

This study aimed to evaluate the biological and mechanical behavior of peri-implant bone tissue in implants manufactured in cp-Ti with machined surfaces (CPMS) and modified by LASER (CPLS) and implants manufactured in Ti6Al4V with machined surfaces (ALLOYMS) and modified by LASER (ALLOYLS). The surfaces were analyzed using scanning electron microscopy coupled with X-ray dispersive energy spectroscopy (SEM-EDX) prior to experimental surgery. Ninety-six (2x4mm) implants were installed in surgical beds milled in the right and left tibias of 48 male Wistar rats, one implant of each material (metal) or surface installed in each tibia. Biomechanical analysis was performed using the implant removal torque in all groups in the periods of 14, 21 and 42 days postoperatively and the tibias were sectioned and processed for histological and immunohistochemical analysis. The data obtained in the biomechanical analysis were submitted to statistical analysis (p < 0.05). The SEM-EDX before the installation of the implants showed a difference between the surfaces machined and modified by LASER, regardless of the metal of the implant. The removal torque of ALLOYLS was statistically higher than CPLS, CPMS and ALLOYMS in 14 and 21 days (p < 0.05), as well as CPLS was statistically higher than CPMS and ALLOYMS. In 42 days CPLS and ALLOYLS showed statistical differences when compared to CPMS and ALLOYMS (p < 0.05), however no difference was observed between CPLS and ALLOYLS (p = 0.07). The SEM-EDX of the implants removed by removal torque showed the total bone coverage of the surfaces of CPLS and ALLOYLS, regardless of the analyzed period and a gradual increase in bone coverage on the surfaces of CPMS and ALLOYMS in the periods of 14, 21 and 42 days respectively, CPLS in 42 days showed a mature bone tissue. In the qualitative histological analysis, a mature bone can be observed, suggesting an acceleration of the repair process in the CPLS and ALLOYLS groups. For immunohistochemical analysis, a higher expression of OPN (osteopontin) was observed for the ALLOYLS groups in 14 and 21 days, arising from higher cellular activation. The implants with surface modification by LASER beam, regardless of the material manufactured, provided important physical-chemical modifications on the surface, allowing better mechanical resistance with bone tissue and acceleration of the osseointegration process when compared to implants with machined surfasse(AU)

Influence of radiopaque fillers on physicochemical properties of a model epoxy resin-based root canal sealer

Objective: To verify the influence of radiopaque fillers on an epoxy resin-based sealer. Material and Methods: Experimental sealers were formulated by adding 20%, 40%, 60%, 80%, 100% and 120% of calcium tungstate, ytterbium trifluoride or barium sulphate by weight to an epoxy-resin-base. Setting time, flow, film thickness, radiopacity, sorption, solubility, pH and push-out bond strength were evaluated. Results: The setting time ranged from 373 to 612.66 min, the flow varied from 13.81±0.49 to 22.49±0.37 mm, and the film thickness ranged from 16.67±5.77 to 33.33±11.54 µm. The lowest pH was 5.47±0.53, and the highest was 6.99±0.03. Radiopacity varied from 0.38±0.04 to 2.57±0.21 mmAl and increased with the amount of filler. Calcium tungstate sealers had a higher sorption and solubility than other sealers. There was no significant difference in the push-out bond strength among the fillers at the 120% concentration. CONCLUSION: The inorganic fillers evaluated and their concentrations affect the physicochemical properties of an epoxy resin-based root canal sealer. .