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Set 3000gct x

Manufactured by Shimadzu
Sourced in Japan

The SET-3000GCT/X is a gas chromatography-time of flight mass spectrometry (GC-TOFMS) system produced by Shimadzu. It is designed for high-throughput and sensitive analysis of complex samples. The system combines gas chromatography separation with time-of-flight mass spectrometry detection, providing rapid and accurate identification and quantification of analytes.

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Lab products found in correlation

2 protocols using set 3000gct x

1

Quantitative [11C]raclopride PET Imaging with Eminence Scanner

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PET studies with [11C]raclopride were performed using an Eminence SET-3000GCT/X (Shimadzu Corp., Kyoto, Japan). This scanner provides 99 planes with a 26-cm axial field of view, and the intrinsic spatial resolution was 3.4 mm in-plane and 5.0 mm full-width at half maximum (FWHM) axially (25 (link)). A 10-min transmission scan was acquired before an emission scan using a 137Cs line source for subsequent attenuation correction. [11C]raclopride was administered by the dual-bolus method or bolus-infusion method, and emission data were acquired in three-dimensional mode. The list-mode data were rebound to sinograms and reconstructed by filtered back-projection using a Gaussian filter (cutoff frequency, 0.3 cycle/pixel). The reconstructed in-plane resolution was 7.5 mm in FWHM and the voxel size of the reconstructed images was 2.0 × 2.0 × 2.6 mm. The head movement of each frame was corrected by frame-by-frame image realignment with attenuation correction using a resliced μ-map, as reported previously (26 (link)).
T1-weighted magnetic resonance (MR) images were acquired with a GE 3.0-T Excite system (slice thickness 1.0 mm; matrix, 256 × 256; field of view, 25 × 25 cm).
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2

Multimodal Brain Imaging of Dopamine Receptors

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All subjects underwent a PET scan with [11C]raclopride, a D2/3 receptor radioligand. Among them, 17 individuals (age, 22 ± 0.9 years) also completed a PET scan with [18F]FE‐PE2I, a DAT radioligand. Injection doses of [11C]raclopride and [18F]FE‐PE2I were 222.1 ± 15.5 MBq and 185.3 ± 20.7 MBq, respectively, and molar activities of [11C]raclopride and [18F]FE‐PE2I were 210.0 ± 61.7 GBq/μmol and 410.5 ± 319.1 GBq/μmol, respectively. With regard to the 17 subjects undergoing both the PET scans with [11C]raclopride and [18F]FE‐PE2I, [18F]FE‐PE2I PET scan was begun 2 hr after the start of [11C]raclopride PET. PET images were acquired using a PET camera (SET‐3000GCT/X, Shimadzu, Kyoto, Japan), with the imaging session consisting of 35 frames of increasing duration from 30 s to 5 min over 60 min for [11C]raclopride and 38 frames over 90 min for [18F]FE‐PE2I. Scatter correction was performed by a hybrid scatter correction method based on acquisition with dual‐energy window setting (Ishikawa et al., 2005 ). A 4‐min transmission scan using a 137Cs line source was obtained to correct for attenuation.
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