This is a GATE-simulation study of the Siemens Biograph DUO PET/CT system. It reports effects of changes in the thickness of the employed Lutetium Oxyorthosilicate(LSO) detectors. The PET/CT, a human body phantom and ...This is a GATE-simulation study of the Siemens Biograph DUO PET/CT system. It reports effects of changes in the thickness of the employed Lutetium Oxyorthosilicate(LSO) detectors. The PET/CT, a human body phantom and a cylindrical F-18 FDG source were simulated. Validation measurements were conducted. The results indicate that LSO thickness increase degrades spatial resolution, improves relative energy resolution from 9.0% to 11.3% and increases signal-to-noise-ratio from 0.81 to 1.17. Thicker LSO crystals present greater axial sensitivity so as the detection efficiency of PET would be significantly enhanced.展开更多
Arginine-glycine-aspartic acid （RGD） dendrimer-based nanopatterns on poly（L- lactic acid） were used as bioactive substrates to evaluate the impact of the RGD local surface density on the chondrogenic induction of ...Arginine-glycine-aspartic acid （RGD） dendrimer-based nanopatterns on poly（L- lactic acid） were used as bioactive substrates to evaluate the impact of the RGD local surface density on the chondrogenic induction of adult human mesenchymal stem cells. During chondrogenic commitment, active extracellular matrix （ECM） remodeling takes place, playing an instructive role in the differentiation process. Although three-dimensional environments such as pellet or micromass cultures are commonly used for in vitro chondrogenic differentiation, these cultures are rather limited with respect to their ability to interrogate cells in celI-ECM interactions. In the present study, the nanopatterns of the tunable RGD surface density were obtained as a function of the initial dendrimer concentration. The local RGD surface density was quantified through probability contour plots for the minimum interparticle distance, constructed from the corresponding atomic force microscopy images, and correlated with the cell adhesion and differentiation response. The results revealed that the local RGD surface density at the nanoscale acts as a regulator of chondrogenic commitment, and that intermediate adhesiveness of cells to the substrates favors mesenchymal cell condensation and early chondrogenic differentiation.展开更多
文摘This is a GATE-simulation study of the Siemens Biograph DUO PET/CT system. It reports effects of changes in the thickness of the employed Lutetium Oxyorthosilicate(LSO) detectors. The PET/CT, a human body phantom and a cylindrical F-18 FDG source were simulated. Validation measurements were conducted. The results indicate that LSO thickness increase degrades spatial resolution, improves relative energy resolution from 9.0% to 11.3% and increases signal-to-noise-ratio from 0.81 to 1.17. Thicker LSO crystals present greater axial sensitivity so as the detection efficiency of PET would be significantly enhanced.
文摘Arginine-glycine-aspartic acid （RGD） dendrimer-based nanopatterns on poly（L- lactic acid） were used as bioactive substrates to evaluate the impact of the RGD local surface density on the chondrogenic induction of adult human mesenchymal stem cells. During chondrogenic commitment, active extracellular matrix （ECM） remodeling takes place, playing an instructive role in the differentiation process. Although three-dimensional environments such as pellet or micromass cultures are commonly used for in vitro chondrogenic differentiation, these cultures are rather limited with respect to their ability to interrogate cells in celI-ECM interactions. In the present study, the nanopatterns of the tunable RGD surface density were obtained as a function of the initial dendrimer concentration. The local RGD surface density was quantified through probability contour plots for the minimum interparticle distance, constructed from the corresponding atomic force microscopy images, and correlated with the cell adhesion and differentiation response. The results revealed that the local RGD surface density at the nanoscale acts as a regulator of chondrogenic commitment, and that intermediate adhesiveness of cells to the substrates favors mesenchymal cell condensation and early chondrogenic differentiation.
