数字农科院2.0

Direct Determination Of Ultratrace Arsenic In Blood Samples Using An In-Situ Dielectric Barrier Discharge Trap Coupled With Atomic Fluorescence Spectrometry

文献类型： 外文期刊

作者： Liu, MT; Mao, XF; Liu, JX; Ding, L; Na, X; Chen, GY; Qian, YZ

作者机构：

期刊名称： ATOMIC SPECTROSCOPY

ISSN： 0195-5373

年卷期： 2019 年 40 卷 3 期

页码：

收录情况： JCR（2021版）

摘要： A novel direct sampling hydride generation (HG) system was utilized and is first reported to introduce a blood sample into a in-situ dielectric barrier discharge atomic fluorescence spectrometer (DBD-AFS) for ultratrace determination of arsenic based on the gas phase enrichment (GPE) principle. The in-situ DBD unit was fitted with three concentric quartz tubes to replace the conventional atomizer in the AFS. Followed by a simple disruption for 2 minutes and centrifugation for 8 minutes of the blood sample in 3% HNO3 (v:v) extractant, the arsenic extraction and protein precipitation can be achieved up to 40 multiple dilutions. A supernatant consisting of 5% HCl (v:v) and 5 g/L KBH4 in 1.5 g/L KOH was introduced into the HG-in-situ DBD-AFS. Then, arsenic generating from the HG was trapped using 11 kV DBD at 110 mL/min air, swept for 190 seconds at 500 mL/min Ar, and released with 13 kV at 180 mL/min H-2. Under the optimal conditions, the linear regression coefficient (R-2) was 0.996 ranging from 0.05 to 300 mu g/L. The method detection limit (LOD) obtained was 7 pg arsenic, with a 3.9% precision using 11 repeated measurements for real blood samples. The spiked recoveries for the real blood samples were 96-107%. Furthermore, it was found that the arsenic concentrations measured by the proposed method were not significantly different (P > 0.05) from using microwave digestion in ECP-MS. The complete analysis, including sample pre-treatment, was performed within 15 minutes. The results show that the proposed method offers a fast and reliable analysis of ultratrace levels of arsenic in real blood samples.

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