Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Phys Med Biol ; 58(14): 4865-79, 2013 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-23787497

RESUMO

The purpose of this paper was to investigate the effect of photon flux on the recorded energy spectrum and images produced with a photon-counting detector. We used a photon-counting cadmium telluride (CdTe) x-ray detector (model PID350, Oy Ajat, Finland). The CdTe array was composed of 16 384 pixels, each 0.35 × 0.35 × 0.75 mm(3) in dimension. The photon flux is controlled by an additional aluminum filter (1, 10, 20, 30 and 40 mm). Images were acquired at three different tube voltages (50, 70 and 90 kVp) with various thicknesses of photon flux control (PFC) filters. The data acquisition time was changed to acquire an approximately equal number of counts within the selected energy window between different thicknesses of PFC filters at the same tube voltage. A phantom was manufactured to evaluate the photon flux effect on the image. The phantom was made from polymethyl methacrylate and four concentrations of iodine. The photon flux effect on the image was evaluated by the signal-difference-to-noise ratio (SDNR) between iodine and the background material. The changes of photon flux affected the recorded energy spectra and image. The thickness of the PFC filter that showed the maximum SDNR differed according to the tube voltage. The 10 mm PFC filter showed the highest SDNR at 50 and 70 kVp, while the 30 mm PFC filter exhibited the highest SDNR at 90 kVp. The SDNR was improved up to, on average, 30-fold in optimal photon flux conditions which acquired a spectrum including the lowest electronic noise with no pulse pile-up effect. The results of this study showed that the photon flux affected not only the acquired energy spectrum but also the image. Based on these results, the spectral distortion correction should be considered in connection with the image that is the ultimate purpose of medical imaging.


Assuntos
Fótons , Tomografia Computadorizada por Raios X/métodos , Compostos de Cádmio , Imagens de Fantasmas , Telúrio
2.
Bioorg Med Chem Lett ; 11(12): 1599-603, 2001 Jun 18.
Artigo em Inglês | MEDLINE | ID: mdl-11412989

RESUMO

The 5-HT(3) receptor binding affinities of nine pairs of aryl-substituted arylguanidines and arylbiguanides were examined and the results suggest the likelihood that both classes of agents utilize common receptor binding features. The effects of structural modification were also examined using CoMFA. 1-(3,4,5-Trichlorophenyl)guanidine (5-HT(3) K(i)=0.7 nM) was identified as a very high-affinity arylguanidine. The structures of the high-affinity arylguanidines are inconsistent with current 5-HT(3) pharmacophore models.


Assuntos
Guanidinas/metabolismo , Receptores de Serotonina/metabolismo , Animais , Guanidinas/química , Células Híbridas , Camundongos , Modelos Moleculares , Ligação Proteica , Ensaio Radioligante , Ratos , Receptores de Serotonina/química , Receptores 5-HT3 de Serotonina , Antagonistas da Serotonina/química , Antagonistas da Serotonina/metabolismo , Agonistas do Receptor de Serotonina/química , Agonistas do Receptor de Serotonina/metabolismo , Relação Estrutura-Atividade , Especificidade por Substrato , Células Tumorais Cultivadas
3.
Mol Cells ; 8(1): 96-100, 1998 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-9571638

RESUMO

The accurate function of C5 protein, the protein component of Escherichia coli RNase P, is uncertain in vivo. A controllable expression system for C5 protein was constructed which can be used to investigate effects of C5 protein on various cellular functions including biosynthesis of RNase P in vivo. The semisynthetic rnpA gene encoding C5 protein was fused to the tac promoter of the pKK223-3 expression vector. This tac promoter expression system produced a high level of C5 protein upon induction with isopropyl-beta-D-thiogalacto-pyranoside. When the overexpressed C5 protein was purified and used for reconstitution of RNase P, the reconstituted enzyme was active. The N-terminal amino acid of the overexpressed C5 protein was leucine specified by the second codon of the rnpA gene. The more controllable expression system was constructed by introducing the lacIq gene into the vector sequence itself.


Assuntos
Proteínas de Bactérias/biossíntese , Endorribonucleases/biossíntese , Proteínas de Escherichia coli , Regiões Promotoras Genéticas/genética , RNA Catalítico/biossíntese , Proteínas de Bactérias/genética , Proteínas de Bactérias/fisiologia , Sequência de Bases , Endorribonucleases/efeitos dos fármacos , Endorribonucleases/genética , Escherichia coli/enzimologia , Escherichia coli/genética , Isopropiltiogalactosídeo/farmacologia , Dados de Sequência Molecular , Plasmídeos/genética , Regiões Promotoras Genéticas/efeitos dos fármacos , RNA Catalítico/efeitos dos fármacos , RNA Catalítico/genética , Ribonuclease P
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA