Evidence map›Paper›PMID 41978153›Full record

ArticleNutrients2026

Bioavailability of Functional Iron in Protein Microparticles.

Saranya Chaiwaree, Radostina Georgieva, Till Deckart, Juliane Lenz, Thawanrat Choonukoolphong, Sureeporn Suriyaprom, Ausanai Prapan, Nitsanat Cheepchirasuk, Axel Pruß, Yu Xiong and 2 more

Abstract read
In one paragraph

Article in Nutrients, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Saranya ChaiwareeInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-7209-7687
Radostina GeorgievaInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0003-1546-5540
Till DeckartInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0009-0003-9601-9282
Juliane LenzInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0009-0005-2858-820X
Thawanrat ChoonukoolphongInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.
Sureeporn SuriyapromDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.ORCID 0009-0006-6827-9564
Ausanai PrapanInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0003-1494-1680
Nitsanat CheepchirasukInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0009-0001-7011-8595
Axel PrußInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-0225-7358
Yu XiongInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-2445-8185
Yingmanee TragoolpuaDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.ORCID 0000-0002-0754-0638
Hans BäumlerInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-2573-2289

Funding

European Union, EFRE 10169193
6 · The paper itself

Abstract

backgroundIron deficiency remains a major nutritional challenge, partly due to the limited stability and bioavailability of conventional iron formulations in foods and during digestion. In this study, iron-protein microparticles (IP-MPs) based on bovine serum albumin (IA-MPs) and hemp protein (IH-MPs) were developed via coprecipitation and evaluated as food-compatible iron delivery systems.

methodsIron-protein microparticles (IP-MPs) were fabricated by a coprecipitation technique. The stability of IP-MPs was investigated in a three-phase digestion model. The uptake of IP-MPs by Caco-2 cells as well as the Ferritin concentration in Caco-2 cells were investigated.

resultsParticle morphology and size distribution were strongly dependent on the protein matrix, with hemp protein microparticles exhibiting greater size uniformity and higher stability under simulated gastric conditions. In a standardized in vitro gastrointestinal digestion model, both IP-MP formulations preserved iron predominantly in the bioactive Fe(II) state and remained sufficiently intact to reach the intestinal phase. Biocompatibility and iron uptake were assessed using Caco-2 cell monolayers. Neither formulation induced cytotoxic effects, while iron delivered via IP-MPs showed enhanced cellular uptake compared to a commercial iron supplement and ferrous sulfate. The amount of Fe(II) detected in the basolateral compartment of IH-MP and IA-MP samples (1.4 µg and 1.3 µg, respectively) was higher than that observed for Floradix

conclusionsThese results demonstrate that iron-protein microparticles, particularly those based on hemp protein, effectively improve iron stability during digestion and enhance cellular iron bioavailability, highlighting their potential for application in iron fortification and functional food systems.

Indexed as

IronSerum Albumin, BovineAnimalsBiological AvailabilityCaco-2 CellsDigestionFerritinsHumansParticle SizeFerritinsIronSerum Albumin, BovineCaco-2 celliron bioavailabilityprotein microparticles

Identifiers

PMID41978153
PMCPMC13074657

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.