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1.
Langmuir ; 28(36): 13066-71, 2012 Sep 11.
Artigo em Inglês | MEDLINE | ID: mdl-22920917

RESUMO

Poly(ortho-phenylenediamine) synthesis enabled by the catalytic oxidase-like activity of nanoceria was accomplished for applications in electronics, medicine, and biotechnology. The polymer shows unique morphology, conductivity, and photoluminescence based on pH of the solution during synthesis. The various poly(ortho-phenylenediamine) preparations were characterized by UV-visible spectroscopy, scanning electron microscopy, fluorescence spectroscopy, fluorescence microscopy, high-pressure liquid chromatography, and cyclic voltammetry. Poly(ortho-phenylenediamine) synthesized at pH 1.0 by nanoceria was selected to be extensively studied on the basis of the fast synthetic kinetics and the resulting conductive and photoluminescent properties for various applications.


Assuntos
Cério/química , Luminescência , Fenilenodiaminas/síntese química , Condutividade Elétrica , Concentração de Íons de Hidrogênio , Tamanho da Partícula , Fenilenodiaminas/química
2.
Cancers (Basel) ; 14(21)2022 Oct 25.
Artigo em Inglês | MEDLINE | ID: mdl-36358642

RESUMO

Metabolic tumor volume (MTV) is a robust prognostic biomarker in diffuse large B-cell lymphoma (DLBCL). The available semiautomatic software for calculating MTV requires manual input limiting its routine application in clinical research. Our objective was to develop a fully automated method (AM) for calculating MTV and to validate the method by comparing its results with those from two nuclear medicine (NM) readers. The automated method designed for this study employed a deep convolutional neural network to segment normal physiologic structures from the computed tomography (CT) scans that demonstrate intense avidity on positron emission tomography (PET) scans. The study cohort consisted of 100 patients with newly diagnosed DLBCL who were randomly selected from the Alliance/CALGB 50,303 (NCT00118209) trial. We observed high concordance in MTV calculations between the AM and readers with Pearson's correlation coefficients and interclass correlations comparing reader 1 to AM of 0.9814 (p < 0.0001) and 0.98 (p < 0.001; 95%CI = 0.96 to 0.99), respectively; and comparing reader 2 to AM of 0.9818 (p < 0.0001) and 0.98 (p < 0.0001; 95%CI = 0.96 to 0.99), respectively. The Bland-Altman plots showed only relatively small systematic errors between the proposed method and readers for both MTV and maximum standardized uptake value (SUVmax). This approach may possess the potential to integrate PET-based biomarkers in clinical trials.

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