Sensitive method for analysis of strontium in human and animal plasma by graphite furnace atomic absorption spectrophotometry

1995 ◽  
Vol 41 (8) ◽  
pp. 1159-1163 ◽  
Author(s):  
R Barto ◽  
A J Sips ◽  
W J van der Vijgh ◽  
J C Netelenbos

Abstract For long-term pharmacokinetic studies in humans as well as in experimental animals, an analysis of strontium (Sr) with a low detection limit and high sensitivity is necessary. The data presented here describe the optimization of the furnace program and sample handling for measuring Sr in plasma by using graphite furnace atomic absorption spectrophotometry. The method was validated and applied to studies on the pharmacokinetics of SrCl2 in humans and rats. Calibration curves were linear up to 57.1 nmol/L. The limit of detection and lower limit of quantification were 0.21 and 0.57 nmol/L, respectively. Reciprocal sensitivity was 0.53 nmol/L Sr at A = 0.0044. The intraassay precision was 2.2%, 1.5%, and 1.1% (n = 6) at 4.57, 22.7, and 49.2 nmol/L Sr, respectively. At these concentrations, the interassay precision and recovery were 0.7%, 1.5%, and 1.8% and 100.4%, 99.1%, and 100.6% (n = 12), respectively. The endogenous Sr concentration in human plasma samples was 0.27 +/- 0.07 mumol/L (n = 18). Pharmacokinetic studies in a human volunteer and in rats demonstrated that this procedure was suited for measuring low Sr concentrations and was applicable to small sample volumes.

Author(s):  
Dong Kim Nguyen ◽  
Ngân Thi kim Lâm

<p><strong>Abstract: </strong>A Graphite Furnace - Atomic Absorption Spectrophotometry (GF-AAS) for the quantification of cadmium (Cd) and lead (Pb) in dried stevia leaves were developed and validated. The method was validated for some parameters, namely linearity and range, precision, accuracy, Limit of Detection (LoD) and Limit of Quantification (LoQ), according to International Conference on Harmonization (ICH). The developed method was linear over the concentration ranging 0 - 2 µg/L (Cd) and 0 – 20 µg/L (Pb). The correlation coefficient (r) obtained for two metal are higher than 0.995. Limit of detection (LOD) of Cd and Pb  was 0.12 µg/L, 0.33 µg/L. The recovery and repeatability in this method were good enough for determining these heavy metals in dried stevia leaves sample.The developed method has been applied successfully for determination of Cd and Pb levels in dried stevia leaves in Vietnam.</p><p class="Default"><strong>Keywords: Stevia, Atomic Absorption Spectrophotometera (AAS), recovery, detection limit, validation.</strong></p>


1985 ◽  
Vol 31 (2) ◽  
pp. 274-276 ◽  
Author(s):  
K F Hallis ◽  
N A Boon ◽  
C M Perkins ◽  
J K Aronson ◽  
D G Grahame-Smith

Abstract This method for determination of Rb+ in human plasma and erythrocytes by graphite-furnace atomic absorption spectrophotometry has a sensitivity of 29 nmol/L for plasma, 12 nmol/L for erythrocytes. The detection limit is 24 nmol/L for plasma, 4.8 nmol/L for erythrocytes. This assay is approximately 30-fold more sensitive than previously reported techniques involving atomic absorption spectrophotometry, enabling use of smaller samples. The rubidium signal is linear with concentration up to 1.2 mumol/L, and addition of other cations to the matrix produces only minor alterations in the Rb+ signal. We measured plasma and erythrocytic Rb+ concentrations in healthy subjects and in patients with untreated essential hypertension. In both, our values are similar to those previously reported for healthy individuals.


1997 ◽  
Vol 80 (6) ◽  
pp. 1287-1297 ◽  
Author(s):  
Paul A Brereton ◽  
Paul Robb ◽  
Christine M Sargent ◽  
Helen M Crews ◽  
Roger Wood ◽  
...  

Abstract An interlaboratory study of a graphite furnace atomic absorption spectrophotometry (GFAAS) method for the determination of lead in wine was conducted. Seventeen laboratories from France, United States, and the United Kingdom, using a variety of GFAAS instruments, took part in the study. The method incorporated a novel matrix-matching procedure to minimize matrix effects between standards and samples. Six wine test materials were prepared and sent to participants as 12 blind duplicate or split level samples. There was good agreement between results obtained from participants and target values (24–279 μg/L) obtained with an inductively coupled plasma-mass spectrometry method. The precision of the GFAAS method was well within the range predicted by the Horwitz equation for the 6 test materials analyzed. Repeatability standard deviations ranged from 3 to 17%. Reproducibility standard deviations were in the range of 10 to 30%. The method is recommended for use for official purposes.


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