[Physical Properties of Small Focal Spot Imaging with Deep Learning Reconstruction in Chest-abdominal Plain CT].

PURPOSE: The aim of this study was to compare the physical properties of small focal spot imaging with deep learning reconstruction (DLR) and small or large focal spot imaging with hybrid iterative reconstruction (IR) in chest-abdominal plain computed tomography. METHOD: In small focal spot imaging using DLR and hybrid IR, tube currents were set at 350 mA. For the large focal spot imaging using hybrid IR, the tube current was set at 360, 400, 450, and 500 mA. The spatial frequencies with 50% task transfer function (TTF) for delrin and acrylic were calculated to compare spatial resolution properties for lung and soft tissue in the chest. Additionally, the low-contrast object-specific contrast-to-noise ratio (CNRLO) was measured as noise property was measured for a 7-mm module with a CT value contrast of 10 HU in the abdomen. RESULT: Spatial frequencies with 50% TTF for delrin and acrylic were found to be greater in small focal spot imaging using DLR compared to those in small and large focal spot imaging using hybrid IR. Moreover, the CNRLO obtained from small focal spot imaging with DLR was also nearly equivalent to that of large focal spot imaging with hybrid IR at tube currents of 450 and 500 mA. CONCLUSION: In chest-abdominal plain computed tomography, small focal spot imaging with DLR has been demonstrated to exhibit greater spatial resolution properties compared to small and large focal spot imaging with hybrid IR, with equivalent or better noise performance.

[Contrast-enhancement Effects of Dual-peak Contrast Medium Injection Method Using Bolus-tracking Technique in Coronary and Aorta CT Angiography].

OBJECTIVE: We compared the contrast-enhancement effects of the coronary arterial phase and the aortic phase in coronary and aorta computed tomography angiography (CA-CTA) using the bolus-tracking technique-based single-peak contrast medium injection (BT-SPI) method and the bolus-tracking technique-based dual-peak contrast medium injection (BT-DPI) method. METHOD: CA-CTA images were acquired from 30 patients, using BT-SPI and BT-DPI. Regions of interest were selected in the right ventricle and ascending aorta during the coronary arterial phase, and in the aorta during the aortic phase to obtain mean CT values. The mean CT values were used to compare the contrast-enhancement effects of BT-SPI and BT-DPI. RESULTS: The mean CT value of the right ventricle during the coronary arterial phase obtained using BT-SPI (320 Hounsfield unit [HU]) and BT-DPI (83 HU) was significantly different (p<0.05). Using BT-SPI and BT-DPI, the mean CT values of the ascending aorta during the coronary arterial phase were 361 HU and 379 HU, respectively, and those of the aorta during the aortic phase were 436 HU and 437 HU, respectively. The difference in the mean CT values for the aorta between BT-SPI and BT-DPI during the coronary arterial and aortic phases was insignificant. CONCLUSION: The retention of the contrast medium in the right ventricle during the coronary arterial phase using BT-DPI was lower than that using BT-SPI. BT-DPI showed substantial contrast-enhancement effects in both the coronary arterial and aortic phases.

Ring cleavage and successive aldol reaction of 3-[(trialkylsilyl)methyl]cyclobutanones.

3-[(Trialkylsilyl)methyl]cyclobutanones reacted with aldehydes by activation with titanium(IV) chloride to give acyclic ß,γ-unsaturated ß'-hydroxyketones.

Titanium(IV) chloride-mediated carbon-carbon bond-forming reaction between 3,3-dialkylcyclobutanones and aldehydes.

Treatment of 3,3-dialkylcyclobutanones with titanium(IV) chloride in the presence of aldehyde gave beta'-chloro-beta-hydroxy ketones in high yields. It was speculated that ring cleavage of the cyclobutanone ring with titanium(IV) chloride gave trichlorotitanium enolate having a tertiary alkyl chloride moiety and then aldol reaction of the titanium enolate proceeded. A trialkylsilylmethyl group at the 2-position of cyclobutanone facilitated the ring cleavage. Synthesis of substituted cyclopentenone from an obtained product is also described.