Issue 18, 2018

Non-chromatographic separation and determination of thimerosal and inorganic mercury in vaccines by Fe3+-induced degradation with cold vapor atomic fluorescence spectrometry

Abstract

An effective, rapid and inexpensive method without chromatographic separation was proposed for the determination of thimerosal (THM) and inorganic mercury (IHg) in vaccine samples, based on Fe3+-induced degradation of THM in a commercially available atomic fluorescence spectrometer (AFS). In the proposed method, inorganic mercury was measured at a low concentration of KBH4 (0.005%, m/v) in the absence of Fe3+, while the total mercury (THg) was determined by measuring the same fluorescence signals of IHg and THM, which was effectively degraded and reduced in the presence of 10 mg L−1 Fe3+ and a relatively high concentration of KBH4 (1.0%, m/v). Then, the concentration of THM can be obtained by subtracting IHg concentration determined in the absence of Fe3+ from THg concentration in the presence of Fe3+. The parameters influencing mercury determination were optimized in detail, including Fe3+ concentration, the concentration of the KBH4 reductant and HCl carrier, and the carrier gas flow rate. Under the optimized conditions, the limits of detection for THM and IHg were 0.03 μg L−1 and 0.02 μg L−1, respectively. Spiked commercial vaccine samples including hepatitis-B and rabies vaccines were analyzed. Satisfactory recoveries were obtained for both THM and IHg.

Graphical abstract: Non-chromatographic separation and determination of thimerosal and inorganic mercury in vaccines by Fe3+-induced degradation with cold vapor atomic fluorescence spectrometry

Article information

Article type
Paper
Submitted
05 Feb 2018
Accepted
18 Apr 2018
First published
19 Apr 2018

Anal. Methods, 2018,10, 2144-2150

Non-chromatographic separation and determination of thimerosal and inorganic mercury in vaccines by Fe3+-induced degradation with cold vapor atomic fluorescence spectrometry

Q. Xu, Z. Wang, L. Jin, P. Liu, Y. Tian, S. Zhang and C. Zhang, Anal. Methods, 2018, 10, 2144 DOI: 10.1039/C8AY00284C

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