Published December 2018 | Version v1
Journal article

Quantitative assessment of the metabolic products of iron oxide nanoparticles to be used as iron supplements in cell cultures

  • 1. Bundesanstalt für Materialforschung und -prüfung (BAM), Richard-Willstätter Str. 11, 12489, Berlin (Germany)
  • 2. Humboldt-University Berlin, School of Analytical Sciences Adlershof, Unter den Linden 6, 10099, Berlin (Germany)
  • 3. Department of Physical and Analytical Chemistry. Faculty of Chemistry. University of Oviedo, C/Julian Clavería 8, 33006, Oviedo (Spain)

Description

Highlights: • SDS-containing reversed phase liquid chromatography is used for the isolation of iron oxide nanoparticles from inorganic Fe(III) species. • Quantitative nanoparticles recoveries addressed by post-column isotope dilution can be obtained. • Two enterocytes-like cell models show Fe nanoparticle uptake. • Iron NPs metabolic products in cells have been quantitatively addressed. - Abstract: Iron nanoparticles (NPs) metabolism is directly associated to human health due to their use as anemia treatment and should be studied in detail in cells. Here we present a speciation strategy for the determination of the metabolic products of iron oxide nanoparticles coated by tartaric and adipic acids in enterocytes-like cell models (Caco-2 and HT-29). Such methodology is based on the use of SDS-modified reversed phase high performance liquid chromatography (HPLC) separation using inductively coupled plasma-mass spectrometry (ICP-MS) as Fe selective detector. Post-column isotope dilution analysis is used as quantification tool by adding 57Fe as isotopically enriched standard. To assess the separation capability of the method, two different iron nanostructures: iron sucrose nanoparticles -Venofer®- used as model suspension and iron tartrate/adipate-modified nanoparticles, both of about 4 nm (core size) were evaluated. The two nanostructures were injected into the system showing good peak profiles and quantitative elution recoveries (>80%) in both cases. In addition, both nanoparticulate fractions could be based-line separated from ionic iron species, which needed to be complexed with 1 mM citrate to elute from the column. Exposed cells up to 0.5 mM of iron tartrate/adipate-modified nanoparticles were specifically treated to extract the internalized NPs and the extracts examined using the proposed strategy. The obtained results revealed the presence of three different fractions corresponding to nanoparticle aggregates, dispersed nanoparticles and soluble iron respectively in a single chromatographic run. Quantitative experiments (column recoveries ranging from 60 to 80%) revealed the presence of the majority of the Fe in the nanoparticulated form (>75%) by summing up the dispersed and aggregate particles. Such experiments point out the high uptake and low solubilization rate of the tartrate/adipate NPs making these structures highly suitable as Fe supplements in oral anemia treatments.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.aca.2018.08.003

Additional details

Identifiers

DOI
10.1016/j.aca.2018.08.003;
PII
S0003267018309401;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
1039
Journal Page Range
p. 24-30
ISSN
0003-2670
CODEN
ACACAM

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.