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G2500 1kg

Manufactured by Merck Group
Sourced in United States

G2500-1KG is a laboratory equipment product offered by Merck Group. It is a powdered substance with a mass of 1 kilogram. The core function of this product is to serve as a chemical reagent or ingredient used in various laboratory procedures and experiments. No further details about its intended use or application are provided.

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5 protocols using g2500 1kg

1

Fabrication of Gelatin Phantom for Optical Studies

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A 10% homogeneous gelatin phantom with 10 mm thickness was fabricated by using gelatin powder (gel strength 300 type A, G2500–1KG, Sigma-Aldrich, St. Louis, MO, USA) mixed with 1 g titanium dioxide (TiO2) to provide optical scattering. A total volume of 100 mL of tap water in a 500 mL beaker was heated to 70 °C. The 10% v/v gelatin powder and 1 g TiO2 were added with stirring to the beaker for approximately 5 minutes to homogenize the solution. The mixed solution was placed in a de-gassing chamber to remove small bubbles in the fluid. After that, the mixed solution was poured into a regular Petri dish (85 mm × 10 mm) and placed in a 4 °C refrigerator for fast congealing.
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2

Intralipid-Gelatin Phantom for Optical Imaging

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The intralipid-gelatin phantom was made from intralipid (Intralipid 20%, Fresenius Kabi, Sweden), porcine skin gelatin (10% by weight, G2500-1kG, Sigma-Aldrich, USA), and deionized water (42 (link)). With a lipid concentration of 1.5 g ml−1, the reduced scattering coefficient μs was ~10 cm−1. Acrylic spacers with a thickness of 0.15 cm were sandwiched between two acrylic sheets to accurately control the thickness of the intralipid-gelatin phantom to be 0.15 cm (equivalent to 1.5 lt , where lt denotes the transport mean free path).
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3

Fabrication of Intralipid-Gelatin Phantom

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The intralipid-gelatin phantom was made from intralipid (Intralipid 20%, Fresenius Kabi, Sweden), porcine skin gelatin (10% by weight, G2500–1kG, Sigma-Aldrich, USA) and de-ionized water34 . With a lipid concentration of 1.5 g mL–1, the reduced scattering coefficient μs was ~10 cm–1. Acrylic spacers with a thickness of 1 mm were sandwiched between two acrylic sheets to accurately control the thickness of the intralipid-gelatin phantom to be 1 mm.
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4

Fabrication of Vascular Tissue Phantoms

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Blood vessel phantoms were composed of silicon tubing (11–189-15H, Fisher Scientific) with an inner and outer diameter of 1.98 mm and 3.18 mm, respectively. Phantom skin tissue consisted of an 18% gelatin concentration derived from porcine skin (G2500–1KG, Sigma Life Science). The gelatin solution underwent four heating cycles (5 seconds each) in a 1200 W microwave, and was then placed in a 10 × 20 × 1.5 cm 3D-printed box, containing the silicon tubing in order to solidify. The phantom vessels were placed at a depth of 2 mm, measured from the gelatin surface to the outer wall of the tubing. More details associated with the fabrication of tissue phantoms can be found in Chen et al.30 (link). The BMF solution was pumped through the blood vessel phantoms via a peristaltic pump (12 V, #1150, Adafruit Industries) at a rate of 35 ml/min, approximating the resting venous flow rate of healthy adults.
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5

Intralipid-Gelatin Phantom for Optical Imaging

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The intralipid–gelatin phantom was made from intralipid (Intralipid 20%, Fresenius Kabi, Sweden), porcine skin gelatin (10% by weight, no. G2500-1kG, gel strength 300, Sigma-Aldrich, USA) and de-ionized water51 with a lipid concentration of 1.5 g ml−1. The reduced scattering coefficient μS’ was measured by a home-built oblique incidence reflectometer52 (link) to be 9.8 cm−1.
Acrylic spacers with a thickness of 1.5 mm were sandwiched between two acrylic sheets to accurately control the thickness of the intralipid–gelatin phantom to be 1.5 mm (equivalent to 1.5lt ). The clear gelatin-gel layer was made from porcine skin gelatin (10% by weight) and de-ionized water. The optical absorptive target (3.9 mm 1.3 × mm 20.0 × mm along the x, y and z directions) was made from black ink, gelatin and distilled water. The absorption coefficient of the target was 0.80 cm−1, as measured by a spectrophotometer (Cary Eclipse, Varian, USA). The diffuser (DG20-120, Thorlabs, USA) was embedded inside the gelatin gel to position it closer to the absorptive target (distance = 8.0 mm) and the intralipid–gelatin layer (distance = 22.1 mm) without blocking the ultrasonic waves.
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