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Thermo x series quadrupole icp ms

Manufactured by Thermo Fisher Scientific

The Thermo X-Series Quadrupole ICP-MS is a versatile analytical instrument used for the detection and quantification of trace elements in a wide range of sample types. It utilizes inductively coupled plasma as the ion source and a quadrupole mass analyzer for element-specific detection and analysis.

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3 protocols using thermo x series quadrupole icp ms

1

Platinum Content Determination in Samples

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Samples were dissolved in 0.5 mL nitric acid (65%) with a hot plate at 100 °C during 12 h. The solution digest was diluted in ultrapure water to 10 mL, obtained from a MilliQ apparatus. The Pt content was measured by a Thermo X-Series Quadrupole ICP-MS (Thermo Scientific) equipped with Ni cones and a glass concentric nebulizer (Meinhard, 1.0 mL min-1) refrigerated with a Peltier system. Indium (115In) at a concentration of 10 μg L-1 was used as internal standard. Standards were prepared from standard ICP-MS 71 A (Inorganic Venture) with a final concentration of 5.0% nitric acid.
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2

Ruthenium and Boron Cellular Uptake

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For the cellular uptake experiments, A375 human melanoma cells (ca. 1 × 106 cells/5 mL) were seeded into t25 flasks and allowed to adhere overnight in a 5% CO2 incubator at 37 °C. Cells settled for 24 h, followed by the addition of RuCB1 and RuCB2, at a concentration equivalent to their IC50 values found for 24 h challenge at 37 °C. After incubation, cells were washed with ice-cold PBS and treated in order to obtain a cellular pellet. The cytosol, membranes/particulate, cytoskeletal and nuclear fractions were extracted using a FractionPREP™ (BioVision, USA) cell fractionation kit according to the manufacturer's protocol. The Ru (102Ru) and B (10B) content in each fraction was measured by a Thermo X-Series Quadrupole ICPMS (Thermo Scientific) after digestion of the samples and using a procedure similar to a previously described.76 (link)
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3

Cellular Uptake and Fractionation of Ruthenium Complexes

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For the cellular uptake experiments, MCF7 cells (ca. 10 6 cells/ 5 mL medium) were exposed to the complexes at a concentration equivalent to their IC 50 values found for 24 h challenge, 37 C. After incubation cells were then washed with ice-cold PBS and treated in order to obtain a cellular pellet [67] . The cytosol, membrane/particulate, cytoskeletal and nuclear fractions were extracted using a FractionPREPTM, cell fractionation kit (BioVision, USA) and performed according to the manufacturer's protocol. The Ru ( 101 Ru) content in each fraction was measured by a Thermo X-Series Quadrupole ICP-MS (Thermo Scientific) after digestion of the samples and using the same procedure previously described [67] .
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