Signal amplification strategies for clinical biomarker quantification using elemental mass spectrometry

Author(s):  
Andrea L. Larraga-Urdaz ◽  
Maria L. Fernandez Sanchez ◽  
Jorge Ruiz Encinar ◽  
Jose M. Costa-Fernandez
2011 ◽  
Vol 83 (7) ◽  
pp. 2425-2429 ◽  
Author(s):  
R. Kenneth Marcus ◽  
C. Derrick Quarles ◽  
Charles J. Barinaga ◽  
Anthony J. Carado ◽  
David W. Koppenaal

2019 ◽  
Vol 91 (6) ◽  
pp. 3773-3777 ◽  
Author(s):  
Joseph E. Lesniewski ◽  
Kunyu Zheng ◽  
Paolo Lecchi ◽  
David Dain ◽  
Kaveh Jorabchi

2019 ◽  
Vol 34 (3) ◽  
pp. 426-459 ◽  
Author(s):  
Andrew Taylor ◽  
Nicola Barlow ◽  
Martin P. Day ◽  
Sarah Hill ◽  
Nicholas Martin ◽  
...  

This review discusses developments in elemental mass spectrometry, atomic absorption, emission and fluorescence, XRF and LIBS, as applied to the analysis of specimens of clinical interest, foods and beverages. Sample preparation procedures and quality assurance are also included.


1992 ◽  
Vol 46 (3) ◽  
pp. 401-406 ◽  
Author(s):  
George R. Agnes ◽  
Gary Horlick

Preliminary results for the analytical use of electrospray mass spectrometry (ES-MS) for elemental analysis are presented. Spectra with the declustered plus-one ion (M+) as the dominant species have been measured for the alkali metals (Li, Na, K, Rb, and Cs) and for several transition metals (Cr, Mn, Fe, Co, Ni, Cu, Zn, Ag, and Cd) in both aqueous and methanol solvents. A number of background ions are also observed including MH+, MO+, MOH+, and MOH(H2O)+. For vanadyl sulfate and uranyl nitrate, ES conditions can be adjusted to produce VO+ and UO2+ as the dominant ions in the mass spectra, indicating that direct speciation of inorganic solution components is possible. On the basis of these preliminary results, it appears that electrospray may offer a low-cost and simple generic ion source for elemental mass spectrometry.


2013 ◽  
Vol 10 (1) ◽  
pp. 17 ◽  
Author(s):  
Kunichika Nakamiya ◽  
Mitsuha Yoshikane ◽  
Hosoya Tomoko ◽  
Yasuyuki Shibata

Environmental context Contamination of groundwater by arsenic compounds used in chemical warfare research is a recently discovered environmental problem in Japan. We report evidence that the arsenic compounds originally present in the groundwater are transforming to thio-arsenic compounds of currently unknown environmental fate. Abstract During routine analyses of groundwater samples contaminated with diphenylarsinic acid (DPAA) at Kamisu, Ibaraki Prefecture, Japan, we obtained data indicating that unknown arsenic compounds accounted for up to 75% of the total arsenic in some of the samples. Results from using liquid chromatography in combination with elemental mass spectrometry and tandem molecular mass spectrometry suggested that two of the main unknown peaks were diphenyldithioarsinic acid and methylphenyldithioarsinic acid. These assignments were later confirmed by comparison with chemically synthesised compounds. A potential transformation scheme for DPAA in the environment is proposed based on the derivatives identified in the environmental samples.


1994 ◽  
Vol 49 (9) ◽  
pp. 901-914 ◽  
Author(s):  
Konosuke Oishi ◽  
Toyoharu Okumoto ◽  
Takashi Iino ◽  
Masataka Koga ◽  
Toshihiro Shirasaki ◽  
...  

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