Briefly, to prepare the analysis, the decomposition of the organic matrix was achieved by heating it for 10 h at 90 °C after adding 0.8 mL HNO3 and 0.4 mL H2O2 to 1 mL of plasma sample. The samples were then dried at 200 °C on a hot plate. Sample reconstitution was carried out by adding 0.5 mL of nitric acid, 10 μL of indium (10 mg/L) as an internal standard and ultrapure water to bring the solution to 10 mL. Reagent blanks, element standards and certified reference materials (Seronorm, lot 0511545 Sero AS Billingstand, Norway) were prepared identically and used for accuracy testing. Before the analysis, the commercial control materials were diluted according to the manufacturer’s recommendations. Digested solutions were analyzed by an ICP-MS Nexionmodel 300D (PerkinElmer, Inc., Shelton, CT, USA). Samples were analyzed in triplicate. The values of each standard material (10 μg/L) used for quality controls were in agreement with intra and inter-assay coefficient variations of less than 5%.
Nexion model 300d
The Nexion model 300D is an inductively coupled plasma mass spectrometer (ICP-MS) instrument designed for elemental analysis. It provides sensitive and accurate detection of a wide range of elements in various sample types.
Lab products found in correlation
9 protocols using nexion model 300d
Trace Elements Analysis by ICP-MS
Briefly, to prepare the analysis, the decomposition of the organic matrix was achieved by heating it for 10 h at 90 °C after adding 0.8 mL HNO3 and 0.4 mL H2O2 to 1 mL of plasma sample. The samples were then dried at 200 °C on a hot plate. Sample reconstitution was carried out by adding 0.5 mL of nitric acid, 10 μL of indium (10 mg/L) as an internal standard and ultrapure water to bring the solution to 10 mL. Reagent blanks, element standards and certified reference materials (Seronorm, lot 0511545 Sero AS Billingstand, Norway) were prepared identically and used for accuracy testing. Before the analysis, the commercial control materials were diluted according to the manufacturer’s recommendations. Digested solutions were analyzed by an ICP-MS Nexionmodel 300D (PerkinElmer, Inc., Shelton, CT, USA). Samples were analyzed in triplicate. The values of each standard material (10 μg/L) used for quality controls were in agreement with intra and inter-assay coefficient variations of less than 5%.
Multi-elemental Analysis via ICP-MS
Serum Elemental Analysis by ICP-MS
ICP-MS Analysis of Elemental Samples
Trace Mineral Analysis and Hormonal Quantification
The decomposition of the organic matrix was achieved by heating it for 10 h at 90 °C after adding 0.8 mL HNO3 and 0.4 mL H2O2 to 2 mL of plasma samples. The samples were then dried at 200 °C on a hot plate. Sample reconstitution was carried out by adding 0.5 mL of nitric acid, 10 μL of indium (In) (10 mg/L) as an internal standard, and ultrapure water to complete 10 mL. Digested solutions were analyzed with an ICP-MS Nexion model 300D (PerkinElmer, Inc., Shelton, CT, USA). Three replicates were analyzed per sample. The values of the standard materials of each element (10 μg/L) used for quality controls were in accordance with intra and inter-assay coefficient variations of less than 5%.
The hormone quantification was conducted using enzyme-linked immunosorbent assay (ELISA) with an ER-500 (Sinnowa, Germany), using the commercial tests for insulin, cortisol, testosterone, and luteinizing hormone from CisRadioquímica, SA (Madrid, Spain). Hormonal analyses were performed in duplicate by the same technician. Coefficients of variation (between and within) were less than 10% for all biochemical analyses.
Multi-Element Analysis by ICP-MS
Quantitative Elemental Analysis by ICP-MS
Multi-Element Analysis by ICP-MS
Inorganic Elemental Analysis by ICP-MS
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