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Varian 600cd

Manufactured by Agilent Technologies
Sourced in United States

The Varian 600CD is a laboratory instrument designed for chromatographic analysis. It functions as a gas chromatograph, providing the capability to separate and identify the components of a complex mixture. The core purpose of the Varian 600CD is to facilitate analytical testing and quantification of various chemical samples.

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4 protocols using varian 600cd

1

Murine Tumor Radiotherapy Protocol

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Radiotherapy was performed using a Varian 600CD (Varian Medical Systems, Palo Alto, CA) linear accelerator with 6 MV X-ray photon beams. Five separated radiation fields with a size of 2 cm × 2 cm each on the isocenter plane (source to the isocenter plane is 100 cm) were simultaneously formed by utilizing the jaw collimator and the multileaf collimator (MLC). The gantry and collimation angles were 0 degrees to guarantee the beam incident vertically downward. The tumor-bearing mice were anesthetized and placed in customized controlling devices, and they were placed on a 10cm thick solid water phantom with a source-to-tumor distance of 100 cm. To ensure an adequate dose, the tumor of each mouse was placed within 1 cm × 1 cm of the center of each radiation field while the rest of the body was placed away from the radiation fields as far as possible, and a 1.5 cm thick phantom for dose build-up was placed above the mice. Single fraction radiotherapy of 20 Gy dose treatment was applied with a 5 Gy/min absorbed dose rate. All experiments were carried out under the supervision of medical physicists and engineers. A schematic summary of the device and regimen was shown in Figure S7B.
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2

Intensity Modulated Radiation Therapy for Cancer

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All patients were treated with the intensity modulated radiation therapy technique randomly using the Varian-600CD (Varian Medical Systems, Palo Alto, CA, USA) or Helical TomoTherapy (Accuray Inc., Sunnyvale, CA, USA) linac with a prescribed dose of 70 to 80 Gy in 33 to 36 fractions. The treatment plans were designed on Pinnacle3 9.0 treatment planning systems (Philips, Fitchburg, WI, USA) or TomoTherapy Planning System (Accuray Inc., Madison, WI, USA) using computed tomography datasets with a 3-mm slice thickness. The beam energy for all plans was 6 megavolt, and the ultimate goal of optimization for an individual patient plan was that the dose to organs at risk (OARs) can be kept as low as possible while maintaining optimal target coverage and dose uniformity to the target. Twelve of 20 patients received RT concurrent with chemotherapy, depending on their grade of disease.
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3

Irradiation of CD133+ Cells and Tumor-Bearing Mice

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Single cell suspension or monolayer culture for CD133+ cells were irradiated in medium with Varian 600 CD X-ray linear accelerator (Varian Medical Systems, Inc., Palo Alto, CA, USA) at a dose rate of 1, 2, or 3 Gy/min exposed at room temperature. Tumor-bearing mice receive whole brain X-ray radiation for 6 consecutive days at 3 Gy/day under anesthesia, and then tumors were measured by bioluminescence images.
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4

Radiation-Induced Pulmonary Fibrosis in Mice

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Twenty WT mice were randomly divided into two groups: the WT control (WT + Con) group and the WT radiation (WT +RT) group. Twenty AR-knockout mice were randomly divided into two groups: KO + Con group and KO + RT group. Mice were fixed in the prone position in a self-made fixing device and covered a 10-mm bolus material on the surface after being anaesthetized with 10% chloral hydrate (i.p., 400 mg/kg; Sigma, St. Louis, MO, USA). A 6 MV X-ray accelerator (Varian 600C/D, VARIAN Medical System, Palo Alto, CA, USA) was used to replicate the mouse model of RIPF with a single wholechest radiation of 15 Gy, a radiation area of about 3.5 cm × 4.0 cm (from the upper to the two axillary pits and the lower to the xiphoid process of sterna, and the rest was shielded by 10 cm thick lead brick), a source target distance of 100 cm, and a dose rate of 500 cGy/min. Normal control mice were anesthetized without chest radiation. Mice were killed 16 weeks after radiation and lung tissues were collected for follow-up experiments.
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