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Trilogy tx

Manufactured by Agilent Technologies
Sourced in United States

The Trilogy Tx is a laboratory instrument designed for spectroscopic analysis. It combines multiple analytical techniques, including atomic absorption, graphite furnace, and flame atomic absorption, to provide a comprehensive analytical solution for a wide range of sample types and applications.

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Lab products found in correlation

2 protocols using trilogy tx

1

Dosimetric Evaluation of IMRT and VMAT

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The diode detector array ArcCHECK was used for measurement of the real dose distribution of IMRT and VMAT. After acquiring a CT image of the ArcCHECK, virtual treatment plans were prepared for head-neck, lung and prostate cases based on the CT images. In each cancer cases, the IMRT and RapidArc (Varian, Palo Alto, CA, USA) plans were made using photons of 6 MV and 10 MV, respectively, and 12 plans were prepared. The virtual tumor target and OARs were contoured as shown in Fig 1. All of the plans were created using an Eclipse (Varian, Palo Alto, CA, USA) planning system and prepared according to the dose prescription, as shown in Table 1. A clinical linear accelerator (LINAC), Trilogy Tx (Varian, Palo Alto, CA, USA), was used in this study.
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2

Optimized kV-CBCT Imaging Protocol

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We acquired data from the OBI system of Trilogy Tx (Varian Medical Systems). The OBI system has two robotic arms to carry a kilo-voltage X-ray source and a flat panel detector positioned orthogonally to the mega-voltage X-ray source for treatment.
The scanning parameters used in this experiment are summarized in Table 1. It is important to note that we blocked 0.5 cm using a lead blade on the opposite side of copper filter to remove off-axis marginal data from the projections, as discussed in Section I. The dimensions of the intensity-weighting (IW) copper filter are 10 cm × 5.5 cm × 0.6 cm, and it was utilized instead of a half-fan bowtie filter. We selected 6 mm as an appropriate thickness of a copper filter that can achieve substantially reduced radiation exposure (approximately 90%) based on previous work by Cho et al. [11 (link)]. A dose reduction assessment is described in Section II-3.
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