Non-transferrin-bound iron determination in blood serum using microsequential injection solid phase spectrometry- proof of concept.

Talanta

Universidade Católica Portuguesa, CBQF - Centro de Biotecnologia e Química Fina - Laboratório Associado, Escola Superior de Biotecnologia, Rua Diogo Botelho, 1327, 4169-005, Porto, Portugal. Electronic address:

Published: May 2023


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

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 of iron (III), with a limit of detection of 0.49 μmol L and a limit of quantification of 1.62 μmol L. 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.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.talanta.2023.124345DOI Listing

Publication Analysis

Top Keywords

non-transferrin-bound iron
8
solid phase
8
iron
8
iron overload
8
quantification ntbi
8
iron iii
8
ntbi
7
iron determination
4
determination blood
4
blood serum
4

Similar Publications

Iron overload (IOL) is an increasingly recognized complication among pediatric and young adult survivors of hematopoietic stem cell transplantation (HSCT) contributing to significant morbidity and mortality. The pathogenesis of IOL post-HSCT is multifactorial, driven by transfusion burden, impaired erythropoiesis, and increased gastrointestinal iron absorption, leading to toxic non-transferrin bound iron accumulation and oxidative tissue injury. Despite its clinical significance, consensus guidelines for the diagnosis, monitoring, and management of IOL in this population remain limited.

View Article and Find Full Text PDF

Aging also contributes to cancer risk factor potentiation by disturbed iron metabolism and genomic instability, both of which contribute to enhanced risk of cancer, particularly in transfusion-dependent groups such as patients with β-thalassemia or myelodysplastic syndromes. Systemic iron overload results from chronic transfusions and progressively disturbed iron homeostasis and clonal hematopoiesis of indeterminate potential (CHIP) that contribute to oncogenic burden. All these create a permissive profile in which carcinogenesis is favored by oxidative stress, mitochondrial dysfunctions, immune suppression, and disrupted DNA repair.

View Article and Find Full Text PDF

The Relationship Between Non-Transferrin-Bound Iron (NTBI), Labile Plasma Iron (LPI), and Iron Toxicity.

Int J Mol Sci

July 2025

SC Medicina ad Indirizzo Metabolico, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.

Plasma non-transferrin-bound iron (NTBI) comprises multiple subspecies, classified by their composition, chemical reactivity, and susceptibility to chelation. The redox-active and chelatable fraction of NTBI is referred to as labile plasma iron (LPI). The pathophysiological significance of NTBI and LPI lies in their ability to enter cells via alternative transport pathways that are not regulated by the transferrin receptor system or by cellular iron levels.

View Article and Find Full Text PDF

Exploring age-related iron dysregulation: effects on longevity, body size, and behavior in C. elegans.

Exp Gerontol

September 2025

Department of Physiology and Aging, College of Medicine, University of Florida, Gainesville, FL 32610, USA; Institute on Aging, University of Florida, Gainesville, FL 32610, USA; Florida Chemical Senses Institute, University of Florida, Gainesville, FL 32610, USA; Genetics Institute, University of F

Age-related iron accumulation is widely observed in various species and significantly impacts physiological processes. However, systematic investigation into how age-related iron dysregulation affects different life traits is still limited. This study utilizes the model organism C.

View Article and Find Full Text PDF

Diagnostics: Markers of Body Iron Status.

Adv Exp Med Biol

July 2025

Department of Medicine, University of Verona and EuroBloodNet Referral Center for Iron Disorders, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

Iron is a micronutrient essential to nearly all living organisms. It plays a pleiotropic role in many vital metabolic processes beyond the classical function in hemoglobin synthesis. Both iron deficiency and iron overload are detrimental in humans, as iron excess can favor the generation of toxic oxygen radicals and cell death by ferroptosis.

View Article and Find Full Text PDF