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1.
J Appl Oral Sci ; 30: e20220227, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36753069

RESUMO

BACKGROUND: To evaluate the release of bisphenol-A glycidyl methacrylate (BisGMA), triethylene glycol dimethacrylate (TEGDMA), bisphenol A (BPA), and phthalates of the composite resin used in the bonding of spurs applied in the treatment of children with anterior open bite and its effects on human keratinocytes. METHODOLOGY: Saliva samples of 22 children were collected before spur attachment (baseline) and 30 minutes (min) and 24 hours (h) after spur bonding. Analysis was performed using high-performance liquid chromatography (HPLC) coupled to tandem mass spectrometry (HPLC-MS/MS) and gas chromatography coupled to mass spectrometry (GC-MS). Standardized resin increments were added to three different dilutions of the cell culture medium. Keratinocytes (HaCaT) were cultivated in the conditioned media and evaluated for cell viability (MTT) and cell scratch assay. RESULTS: The levels of BisGMA (1.74±0.27 µg/mL), TEGDMA (2.29±0.36 µg/mL), and BPA (3.264±0.88 µg/L) in the saliva after 30 min, in comparison to baseline (0±0 µg/mL, 0±0 µg/mL, and 1.15±0.21 µg/L, respectively), presented higher numbers. After 24 h, the levels of the monomers were similar to the baseline. Phthalates showed no significant difference among groups. HaCat cells showed increased viability and reduced cell migration over time after exposure to methacrylate-based resin composites. CONCLUSION: Resin composites, used to attach spurs in children with anterior open bite during orthodontic treatment, release monomers after polymerization and can influence the behavior of human keratinocytes, even at very low concentrations. Orthodontists should be aware of the risks of the resinous compounds release and preventive procedures should be held to reduce patient exposure.


Assuntos
Mordida Aberta , Saliva , Criança , Humanos , Saliva/química , Espectrometria de Massas em Tandem , Ácidos Polimetacrílicos/química , Resinas Compostas/química , Bis-Fenol A-Glicidil Metacrilato/química , Metacrilatos/química , Polietilenoglicóis/química , Teste de Materiais
2.
J. appl. oral sci ; J. appl. oral sci;30: e20220227, 2022. tab, graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1421892

RESUMO

Abstract To evaluate the release of bisphenol-A glycidyl methacrylate (BisGMA), triethylene glycol dimethacrylate (TEGDMA), bisphenol A (BPA), and phthalates of the composite resin used in the bonding of spurs applied in the treatment of children with anterior open bite and its effects on human keratinocytes. Methodology Saliva samples of 22 children were collected before spur attachment (baseline) and 30 minutes (min) and 24 hours (h) after spur bonding. Analysis was performed using high-performance liquid chromatography (HPLC) coupled to tandem mass spectrometry (HPLC-MS/MS) and gas chromatography coupled to mass spectrometry (GC-MS). Standardized resin increments were added to three different dilutions of the cell culture medium. Keratinocytes (HaCaT) were cultivated in the conditioned media and evaluated for cell viability (MTT) and cell scratch assay. Results The levels of BisGMA (1.74±0.27 μg/mL), TEGDMA (2.29±0.36 μg/mL), and BPA (3.264±0.88 μg/L) in the saliva after 30 min, in comparison to baseline (0±0 μg/mL, 0±0 μg/mL, and 1.15±0.21 μg/L, respectively), presented higher numbers. After 24 h, the levels of the monomers were similar to the baseline. Phthalates showed no significant difference among groups. HaCat cells showed increased viability and reduced cell migration over time after exposure to methacrylate-based resin composites. Conclusion Resin composites, used to attach spurs in children with anterior open bite during orthodontic treatment, release monomers after polymerization and can influence the behavior of human keratinocytes, even at very low concentrations. Orthodontists should be aware of the risks of the resinous compounds release and preventive procedures should be held to reduce patient exposure.

3.
Rev. bras. farmacogn ; 28(1): 21-26, Jan.-Feb. 2018. tab, graf
Artigo em Inglês | LILACS | ID: biblio-898747

RESUMO

ABSTRACT The aim of this paper is to provide an overview on the chemical composition of triterpenes in widespread used folk medicine species, through the development and validation of eleven compounds using HPLC-UV detection. The compounds were separated using isocratic elution, on a reverse phase column (Kinetex C18, 250 mm × 4.6 mm, 5 µm) with mobile phase consisted of acetonitrile:tetrahydrofuran (90:10, v/v), flow-rate of 0.5 ml/min and detection in 210 nm. Diverse validation parameters were successfully evaluated. The samples of Bauhinia variegata L., B. variegata var. candida Voigt, Fabaceae, Cecropia palmata Willd. and C. obtusa Trécul, Urticaceae, collected in 2012, 2013 and 2014 from Amazon were treated with two different solvents (ethyl acetate and chloroform) and analyzed by the proposed method. Stigmasterol, lupeol, β-sitosterol, β-amirin and α-amirin were found in all the studied plants. Highlighting the presence of oleanolic acid, maslinic acid in C. obtusa and C. palmata extracts, erythrodiol only in C. palmata, stigmasteol in B. variegata and α-amirin in B. variegata var. candida. Overall, ethyl acetate showed better performance as the extractor solvent than chloroform. Moreover, it could be used for the quality control of medicinal plants and to assess potential marker compounds.

4.
Spectrochim Acta A Mol Biomol Spectrosc ; 173: 749-756, 2017 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-27794240

RESUMO

A novel method was developed to determine low molecular weight polycyclic aromatic hydrocarbons in aqueous leachates from soils and sediments using a salting-out assisted liquid-liquid extraction, synchronous fluorescence spectrometry and a multivariate calibration technique. Several experimental parameters were controlled and the optimum conditions were: sodium carbonate as the salting-out agent at concentration of 2molL-1, 3mL of acetonitrile as extraction solvent, 6mL of aqueous leachate, vortexing for 5min and centrifuging at 4000rpm for 5min. The partial least squares calibration was optimized to the lowest values of root mean squared error and five latent variables were chosen for each of the targeted compounds. The regression coefficients for the true versus predicted concentrations were higher than 0.99. Figures of merit for the multivariate method were calculated, namely sensitivity, multivariate detection limit and multivariate quantification limit. The selectivity was also evaluated and other polycyclic aromatic hydrocarbons did not interfere in the analysis. Likewise, high performance liquid chromatography was used as a comparative methodology, and the regression analysis between the methods showed no statistical difference (t-test). The proposed methodology was applied to soils and sediments of a Brazilian river and the recoveries ranged from 74.3% to 105.8%. Overall, the proposed methodology was suitable for the targeted compounds, showing that the extraction method can be applied to spectrofluorometric analysis and that the multivariate calibration is also suitable for these compounds in leachates from real samples.

5.
Clin Chim Acta ; 428: 9-13, 2014 Jan 20.
Artigo em Inglês | MEDLINE | ID: mdl-24183841

RESUMO

BACKGROUND: Nursing children are exposed to dietary aluminum (in breast milk and/or infant formulas) and through aluminum-adjuvanted vaccines (AAVs). We studied total hair-Al concentrations of nursing children that had been immunized with hepatitis B, DTP, and meningococcal vaccines. METHODS: We studied the hair of 37 young children (aged 26 to 824 days) who were exposed to cumulative doses of Al ranging from 0.63 to 6.88 mg from AAVs. Graphite furnace atomic absorption spectrometry was used to reliably measure total Al concentrations in hair samples. RESULTS: The analytical method proved sensitive enough to quantify Al in the hair of nursing children. At current levels of exposure it is possible to determine total Al in hair sample of 1.65 mg. Cumulative doses of AAV in children ranged from 0.63 to 6.88 mg Al. Median hair-Al was 47.7 µg g⁻¹ (ranging from 12.2 to 221.9 µg g⁻¹). There was no statistically significant correlation between hair-Al concentration and age of child (r=-0.049; p=0.774), total exposure from vaccine (r=-0.078; p=0.643), or the time elapsed after the last AAVs (r=0.015; p=0.931). CONCLUSION: Aluminum in children's hair can be reliably measured but we are still uncertain how representative it can be of the Al body burden.


Assuntos
Adjuvantes Imunológicos/análise , Adjuvantes Imunológicos/química , Alumínio/análise , Cabelo/química , Adjuvantes Imunológicos/administração & dosagem , Brasil , Pré-Escolar , Vacina contra Difteria, Tétano e Coqueluche/administração & dosagem , Vacina contra Difteria, Tétano e Coqueluche/química , Feminino , Vacinas contra Hepatite B/administração & dosagem , Vacinas contra Hepatite B/química , Humanos , Lactente , Recém-Nascido , Masculino , Vacinas Meningocócicas/administração & dosagem , Vacinas Meningocócicas/química , Vacinação
6.
J Periodontol ; 82(9): 1339-52, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21342001

RESUMO

BACKGROUND: The present study is designed as a proof-of-concept study to evaluate light/chemical hardening technology and a newly formulated polymethylmethacrylate, polyhydroxyethylmethacrylate, and calcium hydroxide (PPCH) plus polyanhydride (PA) (PPCH-PA) composite graft material as a bone substitute compared to positive and negative controls in a minipig model. METHODS: PPCH-PA (composite graft); PPCH alone (positive control), PA alone (positive control), and no graft (negative control) were compared. Four mandibular premolar teeth per quadrant were extracted; a total of 48 implants were placed into sockets in three minipigs. Abutments were placed protruding into the oral cavity 4 mm in height for immediate loading. Crestal areas and intrabony spaces were filled with PPCH-PA, PPCH, or PA using a three-phase delivery system in which all graft materials were hardened by a light cure. In the negative control group, implant sites were left untreated. At 12 weeks, block sections containing implants were obtained. Evaluations included periodontal probing, pullout-force load, and stability measurements to determine implant stability, radiographs to examine bone levels, and scanning electron microscopy (SEM)-energy-dispersed spectroscopy to determine bone-to-implant contact. RESULTS: Probing measurements did not reveal any pathologic pocket formation or bone loss. Radiographs revealed that immediate implant placement and loading resulted in bone at or slightly apical to the first thread of the implant in all groups at 12 weeks. Stability test values showed a relative clinical stability for all implants (range: -7 to +1); however, implants augmented with PPCH-PA exhibited a statistically significantly greater stability compared to all other groups (P <0.05). The newly formed bone in PPCH-PA-treated sites was well organized with less marrow spaces and well-distributed osteocytes. SEM revealed a tighter implant-socket interface in the PPCH-PA group compared to other groups with reduced microfissures and implant-bone interface fractures during pullout testing, whereas implants treated with PA or no graft showed ≈ 10-µm microfissures between the implant and bone with fractures of the intrathread bone. CONCLUSIONS: The newly formulated chemically hardened graft material PPCH-PA was useful in immediate implant placement after tooth extraction and resulted in greater stability and a well-organized implant-bone interface with immediate loading, especially in those areas where cancellous bone was present. The results of this proof-of-concept study warranted further research investigating different healing times and longer durations.


Assuntos
Substitutos Ósseos/uso terapêutico , Hidróxido de Cálcio/química , Implantes Dentários , Retenção em Prótese Dentária , Polianidridos/química , Polimetil Metacrilato/química , Processo Alveolar/diagnóstico por imagem , Aumento do Rebordo Alveolar/métodos , Animais , Substitutos Ósseos/efeitos da radiação , Hidróxido de Cálcio/efeitos da radiação , Carga Imediata em Implante Dentário , Masculino , Mandíbula/diagnóstico por imagem , Mandíbula/cirurgia , Teste de Materiais , Microscopia Eletrônica de Varredura , Modelos Animais , Osseointegração/fisiologia , Osteogênese/fisiologia , Bolsa Periodontal/classificação , Polianidridos/efeitos da radiação , Poli-Hidroxietil Metacrilato/química , Poli-Hidroxietil Metacrilato/efeitos da radiação , Polímeros/química , Polímeros/efeitos da radiação , Polimetil Metacrilato/efeitos da radiação , Distribuição Aleatória , Espectrometria por Raios X , Estresse Mecânico , Suínos , Porco Miniatura , Fatores de Tempo , Alvéolo Dental/cirurgia , Microtomografia por Raio-X
7.
Front Oral Biol ; 13: 74-79, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19828974

RESUMO

Amelogenins are the major proteins involved in tooth enamel formation. In the present study, we have cloned and sequenced four novel amelogenins from three amphibian species in order to analyze similarities and differences between mammalian and non-mammalian amelogenins. The newly sequenced amphibian amelogenin sequences were from a red-eyed tree frog (Litoria chloris) and a Mexican axolotl (Ambystoma mexicanum). We identified two amelogenin isoforms in the Eastern red-backed salamander (Plethodon cinereus). Sequence comparisons confirmed that non-mammalian amelogenins are overall shorter than their mammalian counterparts, contain less proline and less glutamine, and feature shorter polyproline tripeptide repeat stretches than mammalian amelogenins. We propose that unique sequence parameters of mammalian amelogenins might be a pre-requisite for complex mammalian enamel prism architecture.


Assuntos
Amelogenina/genética , Anfíbios/genética , Esmalte Dentário/ultraestrutura , Evolução Molecular , Ambystoma mexicanum/genética , Ambystoma mexicanum/metabolismo , Amelogenina/metabolismo , Sequência de Aminoácidos , Anfíbios/metabolismo , Animais , Anuros/genética , Anuros/metabolismo , Sequência de Bases , DNA Complementar/análise , Esmalte Dentário/metabolismo , Mamíferos , Dados de Sequência Molecular , RNA/isolamento & purificação , Homologia de Sequência
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