𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Determination of chromium and nickel in human blood by means of inductively coupled plasma mass spectrometry

✍ Scribed by A. Alimonti; F. Petrucci; B. Santucci; A. Cristaudo; S. Caroli


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
584 KB
Volume
306
Category
Article
ISSN
0003-2670

No coin nor oath required. For personal study only.

✦ Synopsis


The suitability of inductively coupled plasma mass spectrometry (ICP-MS) for the determination Cr and Ni in human whole blood was investigated. Strict criteria for blood sampling and sample treatment were set to avoid contamination or loss of analytes. A wide concentration interval of analytes was obtained by collecting specimens from subjects with a history of exposure to one of the two elements or both. A dynamic range of more than three orders of magnitude was achieved with operative detection limits of 0.03 and 0.04 pg/l in the analytical solution for Cr and Ni, respectively. At 1.0 pg/l and 0.5 pg/l concentration levels for Cr and Ni, respectively, the instrumental precision, as relative standard deviation (R.S.D.), was 2.6% and 3.8%, while for reproducibility of the entire analytical cycle of analysis, including sample pretreatment, values of 4.8% and 5.5% were obtained. The accuracy of the method was verified by using the serum NIST 909 reference material for Cr and an in-house standard for Ni with mean recovery percentages of 95.0% and 105%, respectively. These performance characteristics were obtained by careful evaluation and correction of the interferences at the masses used for determination. For the "*Cr isotope the presence of 4nAr12C, due to the high concentration of C in the organic matter, exerted a dramatic influence. This was overcome only by reduction of the C content of the sample performing a full digestion cycle in a microwave oven and by a suitable correction equation. For Ni measurements, mass 60 gave satisfactory results because of very scarce influence of the main potential interferent ions, i.e., 44Ca'60 and 37C123Na.


πŸ“œ SIMILAR VOLUMES


Determination of Mercury by Inductively
✍ B. Passariello; M. Barbaro; S. Quaresima; A. Casciello; A. Marabini πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 78 KB

To control the amount of mercury polluting our environment, mercury has to be monitored in all areas of modern life. This requires fast and easy-to-use methods that permit the determination of mercury at levels of micrograms per liter. Up to now mercury ultratrace determination has required preconce

Determination of uranium by flow injecti
✍ Joseph H. Aldstadt; Jacqueline M. Kuo; Lesa L. Smith; Mitchell D. Erickson πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 735 KB

A flow injection (FI) system for the on-line determination of uranium in environmental samples has been characterized and tested. The simple FI manifold uses off-the-shelf components to precisely manipulate the carrier, sample, eluent, and washing streams through a column separation module. The sepa

Determination of trace metals in potassi
✍ Naoko Shibata; Noriko Fudagawa; Masaaki Kubota πŸ“‚ Article πŸ“… 1992 πŸ› Elsevier Science 🌐 English βš– 788 KB

Metal lmpurltles contamed m high-punty potassmm hydrogenphthalate reagents were determmed by mductwely coupled plasma mass spectrometry (ICP-MS) with sample mtroductlon by electrothermal vaponzatlon (ETV) The lmpurltles were separated from the matrur constituents by Ion-exchange separation usmg Chel