TY - JOUR
T1 - Non-transferrin-bound iron determination in blood serum using microsequential injection solid phase spectrometry – proof of concept
AU - Miranda, Joana L. A.
AU - Mesquita, Raquel B. R.
AU - Leite, Andreia
AU - Silva, André M. N.
AU - Rangel, Maria
AU - Rangel, António O. S. S.
N1 - Funding Information:
Joana L. A. Miranda thanks the grant NORTE-08-5369-FSE-000007_BD_1. This work received financial support from PT national funds ( FCT / MCTES , Fundação para a Ciência e a Tecnologia and Ministério da Ciência, Tecnologia e Ensino Superior) through the project PTDC/QUI-QIN/28142/2017 . Additionally, the research team would like to thank the projects NORTE-07-0162-FEDER-000048, UIDB/50,016/2020, UIDB/50006/2020. A. Leite thanks FCT for funding through program DL 57/2016 - Norma transitória.
Publisher Copyright:
© 2023 The Authors
PY - 2023/5/15
Y1 - 2023/5/15
N2 - Non-transferrin-bound iron (NTBI) is a group of circulating toxic iron forms, which occur in iron overload or health conditions with dysregulation of iron metabolism. NTBI is responsible for increased oxidative stress and tissue iron loading. Despite its relevance as a biochemical marker in several diseases, a standardized assay is still lacking. Several methods were developed to quantify NTBI, but results show high inter-method and even inter-laboratory variability. Thus, the development of a consistent NTBI assay is a major goal in the management of iron overload and related clinical conditions. In this work, a micro sequential injection lab-on-valve (μSI-LOV) method in a solid phase spectrophotometry (SPS) mode was developed for the quantification of NTBI, using a bidentate 3,4–hydroxypyridinone (3,4-HPO) ligand anchored to sepharose beads as a chromogenic reagent. To attain SPS, the functionalized beads were packed into a column in the flow cell, and the analyte, NTBI retained as iron (III), formed a colored complex at the beads while eliminating the sample matrix. The dynamic concentration range was 1.62–7.16 μmol L−1 of iron (III), with a limit of detection of 0.49 μmol L−1 and a limit of quantification of 1.62 μmol L−1. The proposed μSI-LOV-SPS method is a contribution to the development of an automatic method for the quantification of the NTBI in serum samples.
AB - Non-transferrin-bound iron (NTBI) is a group of circulating toxic iron forms, which occur in iron overload or health conditions with dysregulation of iron metabolism. NTBI is responsible for increased oxidative stress and tissue iron loading. Despite its relevance as a biochemical marker in several diseases, a standardized assay is still lacking. Several methods were developed to quantify NTBI, but results show high inter-method and even inter-laboratory variability. Thus, the development of a consistent NTBI assay is a major goal in the management of iron overload and related clinical conditions. In this work, a micro sequential injection lab-on-valve (μSI-LOV) method in a solid phase spectrophotometry (SPS) mode was developed for the quantification of NTBI, using a bidentate 3,4–hydroxypyridinone (3,4-HPO) ligand anchored to sepharose beads as a chromogenic reagent. To attain SPS, the functionalized beads were packed into a column in the flow cell, and the analyte, NTBI retained as iron (III), formed a colored complex at the beads while eliminating the sample matrix. The dynamic concentration range was 1.62–7.16 μmol L−1 of iron (III), with a limit of detection of 0.49 μmol L−1 and a limit of quantification of 1.62 μmol L−1. The proposed μSI-LOV-SPS method is a contribution to the development of an automatic method for the quantification of the NTBI in serum samples.
KW - Bidentate 3,4-hydroxypyridinone ligand
KW - Iron(III) quantification
KW - Solid phase spectrophotometry
KW - Functionalized beads
KW - NTBI
KW - Serum samples
UR - http://www.scopus.com/inward/record.url?scp=85147846490&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2023.124345
DO - 10.1016/j.talanta.2023.124345
M3 - Article
C2 - 36791595
SN - 0039-9140
VL - 257
JO - Talanta
JF - Talanta
M1 - 124345
ER -