Iron saturation and binding capacity of lactoferrin - development and validation of a colorimetric protocol for quality control

Food Chem. 2025 Jan 15;463(Pt 3):141365. doi: 10.1016/j.foodchem.2024.141365. Epub 2024 Sep 19.

Abstract

Among the numerous biofunctional properties of lactoferrin, its ability to bind iron ions can be considered a core function. The saturation level with ferric iron affects the stability and functionality of the protein. To reliably quantify the iron saturation, an assay based on the color reagent Ferrozine was developed and validated concerning the lower detection (0.023 μg mL-1) and quantification limits (0.069 μg mL-1), as well as precision, recovery and accuracy values. The established assay was used to monitor iron uptake, comparing two commercially available bovine lactoferrin powders. Significant differences between the samples were observed. One sample exhibited nearly ideal binding behavior with a high affinity for ferric iron (saturation > 98 %), while the comparison sample did not exceed saturation values >80 %. This finding underscores the importance of assessing the iron status and binding capacity for the quality evaluation of lactoferrin products.

Keywords: Biofunctional; Ferrozine; Iron quantification; Lactoferrin; Protein bound Iron; Quality; Total Iron binding capacity.

Publication types

  • Evaluation Study
  • Validation Study

MeSH terms

  • Animals
  • Cattle
  • Colorimetry*
  • Iron* / analysis
  • Iron* / chemistry
  • Iron* / metabolism
  • Lactoferrin* / chemistry
  • Lactoferrin* / metabolism
  • Protein Binding
  • Quality Control*

Substances

  • Lactoferrin
  • Iron