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Elan drc e system

Manufactured by PerkinElmer
Sourced in United States, Canada

The Elan DRC-e system is an inductively coupled plasma mass spectrometer (ICP-MS) designed for elemental analysis. It provides high-performance multi-element detection and quantification capabilities.

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2 protocols using elan drc e system

1

Trace Element Analysis of Guangxi Rice

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Rice from Guangxi Province, one of China’s major grain-producing areas, was selected as the object of our study.
Pepsin (catalogue No. 64007137) and pancreatin (catalogue No. 64006737) were purchased from Sinopharm Chemical Reagent Co., Ltd., China, and bile extract (porcine; catalogue No. B822609) was purchased from Macklin, Shanghai, China. All the organic acids used, including citric acid, malic acid, lactic acid and acetic acid, were of analytical purity.
Dietary supplements (vitamin B6 (VB6), vitamin C (VC), vitamin E (VE), folic acid (VB9), niacin (VB3), copper (Cu), methionine (Met) and coenzyme Q10 (Q10) and procyanidins (OPC) were of an excellent level of purity and were purchased from Macklin reagent company.
High-purity deionized water from a Milli-Q Plus system (Millipore, Bedford, MA, USA) was used for dilutions and washes. Element concentrations were determined by inductively coupled plasma optical emission spectrometry (ICP-MS) on an Elan DRC-e system (PerkinElmer, Massachusetts, USA), whose limits of detection (LODs) were 0.1–1 ng g−1 for Se and Zn and less than 0.1 ng g−1 for Cd.
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2

Quantifying Cellular Metal Ions by ICP-MS

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The content of metal ions in AT‐MSCs was determined by inductively coupled plasma mass spectrometry (ICP‐MS). Samples were transferred by concentrated nitric acid into teflon vessels for microwave decomposition (Uniclever BMI−Z, Plazmatronics, Poland). A mixture of 3 mL nitric acid and 1 mL hydrofluoric acid (both Suprapur, Merck, Darmstadt, Germany) was used for sample decomposition. The decomposed samples were transferred to a 50 mL volumetric flask and after appropriate dilution spiked with an internal standard solution (100Rh). Both the calibration solutions and the IS solution were prepared from solutions at a concentration of 1.000±0.002 g/L (Merck). Distilled and demineralized water (conductivity <0.1 μS/cm) (Millipore, Bedford, MA, USA) was used to prepare all solutions.
ICP‐MS measurements were performed using an Elan DRC‐e system (PerkinElmer, Concord, Canada) equipped with a concentric PTFE nebulizer, a cyclonic spray chamber, a high‐efficiency quartz torch, a dynamic reaction cell (DRC) for the elimination of spectral interferences and the Gilson 212 peristaltic pump. Monitored nuclides included 57Fe, 66Zn and 55Mn.
Measurement conditions were: Plasma power 1 100 W, sample uptake 1.2 mL/min, nebulizer Air Flow 0.75 L/min, plasma Air Flow 11 L/min, auxiliary Air Flow 1 L/min, dwell time 50 ms per nuclide, sweeps/reading 10, total acquisition time 20 s.
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