Abstract
Abstract
This method for determining aluminum in serum and urine is essentially free from matrix interference and gives a linear response with concentration to at least 500 micrograms/l. Use of a stabilized temperature platform (L'vov platform, Perkin-Elmer Corp.) to approach a "steady-state" temperature, addition of matrix modifiers [especially Mg(NO3)2], and the use of peak area integration all helped substantially diminish spectral interference. With the platform furnace, serum protein concentrations as great as 260 g/L did not interfere with the determination of Al. The within- and between-assay precision (CV) was less than or equal to 3.5% and less than or equal to 7.4%, respectively. Analytical recovery of Al added to serum ranged between 95 and 101% throughout the linear calibration range (to 500 micrograms/L), either when measured directly from the standard curve or by the method of standard additions. The reference interval for Al in 28 healthy subjects was 2-14 micrograms/L (mean 6.5, SD 4.1 micrograms/L), and for 130 patients on hemodialysis, 20-550 micrograms/L (mean 87.5, SD 62.5 micrograms/L).
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Cited by
46 articles.
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1. Impact of aluminum exposure on lung;Toxicology and Industrial Health;2012-12-20
2. Aluminium [Biomonitoring Methods, 1999];The MAK-Collection for Occupational Health and Safety;2012-01-31
3. Aluminium [Biomonitoring Methods in German language, 1999];The MAK-Collection for Occupational Health and Safety;2012-01-31
4. Acetate inhibition of chick bone cell proliferation and bone growth in vitro;Journal of Bone and Mineral Research;2009-12-03
5. Aluminum: Its Measurement and Metabolism;Seminars in Dialysis;2007-10-01