Advancements in sample preparation for performing elemental analysis are coming from the dissemination of microwave-assisted procedures, but there is still room for improvements by looking for fast and easily applicable procedures. In the present study, the open-vessel digestion sample treatment (19–21 °C or 95 °C) was compared with closed-vessel microwave-assisted digestion (180 °C). Detection and quantification limits, accuracy, precision, residual carbon content, and residual acidity were quantified with certified and in-field hair samples. Human hair samples (0.02 g) were digested with HNO3/H2O2 (2:1) in an open vessel heated to 95 °C. The residual carbon content ˂87 ± 6 mg L-1 and a residual acidity ˂0.86 ± 0.10 mol L-1 in the final digested samples. The elements (Al, As, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Ga, K, La, Li, Mg, Mn, Mo, Na, Nb, Ni, P, Pb, Rb, Sb, Se, Si, Sn, Sr, Te, Ti, Tl, U, V, W, Zn, and Zr) were determined with quadrupole inductively coupled plasma mass spectrometry equipped with a collision-reaction interface. A detection limit (0.00002–30 mg kg-1), precision (repeatability <11% and intermediate precision <13%), trueness bias (-4–9%), and recovery (90–110% for all the elements except for Cr = 65% and Fe = 79%) were observed. The results indicate that the proposed method is suitable for routine multi-elemental analysis in human hair studies.

A new rapid treatment of human hair for elemental determination by inductively coupled mass spectrometry

Migliara, Giuseppe;
2020-01-01

Abstract

Advancements in sample preparation for performing elemental analysis are coming from the dissemination of microwave-assisted procedures, but there is still room for improvements by looking for fast and easily applicable procedures. In the present study, the open-vessel digestion sample treatment (19–21 °C or 95 °C) was compared with closed-vessel microwave-assisted digestion (180 °C). Detection and quantification limits, accuracy, precision, residual carbon content, and residual acidity were quantified with certified and in-field hair samples. Human hair samples (0.02 g) were digested with HNO3/H2O2 (2:1) in an open vessel heated to 95 °C. The residual carbon content ˂87 ± 6 mg L-1 and a residual acidity ˂0.86 ± 0.10 mol L-1 in the final digested samples. The elements (Al, As, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Ga, K, La, Li, Mg, Mn, Mo, Na, Nb, Ni, P, Pb, Rb, Sb, Se, Si, Sn, Sr, Te, Ti, Tl, U, V, W, Zn, and Zr) were determined with quadrupole inductively coupled plasma mass spectrometry equipped with a collision-reaction interface. A detection limit (0.00002–30 mg kg-1), precision (repeatability <11% and intermediate precision <13%), trueness bias (-4–9%), and recovery (90–110% for all the elements except for Cr = 65% and Fe = 79%) were observed. The results indicate that the proposed method is suitable for routine multi-elemental analysis in human hair studies.
2020
human hair analysis
validation
sample preparation
spectroanalytical techniques
human biomonitoring
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14085/21850
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