Evidence map›Paper›PMID 39940163›Full record

ArticleNanomaterials (Basel, Switzerland)2025

Investigation on the Interaction of Dendritic Core Multi-Shell Nanoparticles with Human Red Blood Cells.

Jakob Krauß, Radostina Georgieva, Miroslav Karabaliev, Moritz Hackmann, Pichayut Rerkshanandana, Saranya Chaiwaree, Ulrich Kalus, Axel Pruß, Yu Xiong, Hans Bäumler

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jakob KraußInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.
Radostina GeorgievaInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0003-1546-5540
Miroslav KarabalievDepartment of Medical Physics, Biophysics & Radiology, Medical Faculty, Trakia University, 6000 Stara Zagora, Bulgaria.ORCID 0000-0002-5608-2258
Moritz HackmannInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-4895-2815
Pichayut RerkshanandanaInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-1732-7793
Saranya ChaiwareeInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.
Ulrich KalusInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.
Axel PrußInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.
Yu XiongInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-2445-8185
Hans BäumlerInstitute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-2573-2289

Funding

AiF Projekt ZF4174708AP9
6 · The paper itself

Abstract

The use of nanoparticles is becoming increasingly apparent in a growing number of medical fields. To exploit the full potential of these particles, it is essential to examine their behavior in the blood and their possible interactions with blood cells. Dendritic core multi-shell DendroSol™ nanoparticles (DS-NPs) are able to penetrate into viable layers of human skin, but nothing is known about their interaction with blood cells. In the present study, we analyze the effect of DS-NPs on red blood cells (RBCs) using confocal laser scanning microscopy (CLSM), flow cytometry, sedimentation rate analysis, spectrophotometry, and hemolysis assays. DS-NPs labeled with Nile red (NR) were added to RBC suspensions and their accumulation in the area of the RBC membranes was demonstrated by CLSM as well as by flow cytometry. In the presence of DS-NPs, the RBCs show an increased sedimentation rate, which also confirms the binding of the NPs to the cells. Interestingly, in the presence of DS-NPs, the RBCs are stabilized against hypotonic hemolysis as well as against the hemolytic action of Triton X-100. This proven anti-hemolytic effect could be utilized to enhance the circulation time of RBCs loaded with drugs for prolonged sustained release and drug delivery with enhanced bioavailability.

Indexed as

dendritic core multi-shell carriererythrocyteshemocompatibilityin vivo carriersnanoparticles

Identifiers

PMID39940163
PMCPMC11820349

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Registered trials

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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.