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1.
ACS Omega ; 7(35): 30746-30755, 2022 Sep 06.
Artigo em Inglês | MEDLINE | ID: mdl-36092623

RESUMO

Biodiesel can be altered when exposed to air, light, temperature, and humidity. Other factors, such as microbial or inorganic agents, also interfere with the quality of the product. In the present work, the Rancimat method and mid-infrared spectroscopy associated with chemometry, were used to identify the oxidation process of biodiesel from different feedstocks and to evaluate the antioxidant activity of butylated hydroxytoluene. The study was carried out in four steps: preparation of biodiesel samples with and without the antioxidant agent, degradation of the samples under the effect of light and heating at 70 °C, measurements of the induction period, obtention of infrared spectra, and multivariate analysis. The Fourier transform mid-infrared spectroscopy was used in combination with multivariate analysis, using techniques such as principal component analysis (PCA) and hierarchical clustering analysis (HCA). The Rancimat results showed that babassu biodiesel has a higher resistance to oxidative degradation, while chicken biodiesel is the most susceptible to degradation; on the other hand, the antioxidant activity was more effective with chicken biodiesel, demonstrating that the antioxidant effect depends on the feedstock used in the production of biodiesel. The oxidative stability of babassu oil-, corn oil-, and chicken fat-based biodiesels decreased during storage both in the presence of light and at high temperature. Prior to PCA, all spectra were pre-processed with a combination of Savitzky-Golay smoothing filter with a 7-point window, baseline correction, and mean-centered data. The use of mid-infrared spectroscopy associated with PCA revealed the first two components to explain the greater variability of data, representing over 75% of total variation for all analyzed systems. In addition, it was able to separate the biodiesel samples according to the fatty acid profile of its feedstock, as well as the type of degradation to which it was subjected, the same being confirmed by HCA.

2.
Int J Biol Markers ; 24(4): 277-81, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-20108217

RESUMO

Epidermal growth factor (EGF) plays an important role in cancer. A functional single nucleotide polymorphism (SNP) in the 5'-untranslated region of the EGF gene (+61 A>G) may influence its expression and contribute to cancer predisposition and aggressiveness. Aiming to investigate the role of EGF +61 A>G in the susceptibility to glioma and its prognosis, we performed a case-control study with 165 patients and 200 healthy controls from Brazil. Comparisons of genotype distributions and allele frequencies did not reveal any significant differences between the groups. The mean overall survival was 9.2 months for A/A, 8.2 months for A/G, and 7.7 months for G/G. When survival curves were plotted we found that the +61G allele is associated with poor overall survival (p=0.023) but not with disease-free survival (p=0.527). Our data suggest that, although there is no association between the EGF +61 A>G genotype and glioma susceptibility, this SNP is associated with shorter overall survival of glioma patients in the Brazilian population. Nevertheless, future studies utilizing a larger series are essential for a definitive conclusion.


Assuntos
Fator de Crescimento Epidérmico/genética , Glioma/genética , Polimorfismo de Nucleotídeo Único , Adulto , Idoso , Fator de Crescimento Epidérmico/fisiologia , Feminino , Genótipo , Glioma/etiologia , Glioma/mortalidade , Humanos , Masculino , Pessoa de Meia-Idade , Prognóstico , Fatores de Risco
3.
J Neurooncol ; 90(3): 253-8, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18670736

RESUMO

Werner syndrome (WS) is a premature aging disorder characterized by early onset of symptoms related to normal aging and by a high predisposition to various types of cancer, including gliomas. WS is caused by inherited recessive mutations in the WRN gene, which encodes a helicase considered a caretaker of the genome. Aiming to study the role of WRN Cys1367Arg in glioma susceptibility and oncologic prognosis of patients, we investigated the genotype distribution of this single nucleotide polymorphism in 94 glioma patients and 100 healthy subjects. Comparisons of genotype distributions and allele frequencies did not reveal any significant difference between the groups. Overall and disease-free survival rates were calculated, but no statistically significant difference was observed. Our data suggest that WRN Cys1367Arg SNP is not involved either in susceptibility to developing gliomas or in patient survival, at least in the Brazilian population.


Assuntos
Arginina/genética , Cisteína/genética , Exodesoxirribonucleases/genética , Glioma/diagnóstico , Glioma/genética , Polimorfismo de Nucleotídeo Único/genética , RecQ Helicases/genética , Adulto , Brasil/epidemiologia , Estudos de Casos e Controles , Feminino , Seguimentos , Frequência do Gene , Genótipo , Glioma/epidemiologia , Glioma/mortalidade , Humanos , Masculino , Pessoa de Meia-Idade , Prognóstico , Risco , Análise de Sobrevida , Helicase da Síndrome de Werner
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