Evidence map›Paper›PMID 37881592›Full record

ArticleEnvironment & health (Washington, D.C.)2023

Uptake and Intracellular Fate of Fluorophore Labeled Metal-Organic-Framework (MOF) Nanoparticles.

Ziyao Liu, Andreas Zimpel, Ulrich Lächelt, Maria Pozzi, Marta Gallego Gonzalez, Indranath Chakraborty, Stefan Wuttke, Neus Feliu, Wolfgang J Parak

Open access · diamondAbstract read
In one paragraph

Article in Environment & health (Washington, D.C.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
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

3 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 8 institutions in 5 countries.

Ziyao LiuCenter for Hybrid Nanostructures, Universität Hamburg, 22761 Hamburg, Germany.
Andreas ZimpelDepartment of Chemistry and Center for NanoScience (CeNS), LMU Munich, 81377 Munich, Germany.
Ulrich LächeltDepartment of Pharmacy and Center for NanoScience (CeNS), LMU Munich, 81377 Munich, Germany.ORCID https://orcid.org/0000-0002-4996-7592
Maria PozziCenter for Hybrid Nanostructures, Universität Hamburg, 22761 Hamburg, Germany.
Marta Gallego GonzalezCenter for Cooperative Research in Biomaterials (CIC BiomaGUNE), Basque Research and Technology Alliance (BRTA), 20014 Donostia-San Sebastián, Spain.
Indranath ChakrabortyCenter for Hybrid Nanostructures, Universität Hamburg, 22761 Hamburg, Germany.ORCID https://orcid.org/0000-0003-4195-9384
Stefan WuttkeBCMaterials, Basque Center for Materials, Applications and Nanostructures, UPV/EHU Science Park, 48950 Leioa, Spain.ORCID https://orcid.org/0000-0002-6344-5782
Neus FeliuZentrum für Angewandte Nanotechnologie CAN, Fraunhofer-Institut für Angewandte Polymerforschung IAP, 20146 Hamburg, Germany.ORCID https://orcid.org/0000-0002-7886-1711
Wolfgang J ParakCenter for Hybrid Nanostructures, Universität Hamburg, 22761 Hamburg, Germany.ORCID https://orcid.org/0000-0003-1672-6650
Universität Hamburg · DECenter for NanoScience · DECentral South University · CNCIC biomaGUNE · ESFraunhofer Institute for Applied Polymer Research · DEIkerbasque · ESIndian Institute of Technology Kharagpur · INUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The uptake and the fate of Zr-based metal-organic-framework nanoparticles labeled with organic fluorophores in HeLa cells has been monitored with fluorescence detection and elemental analysis. The nanoparticles have been selected as a model system of carrier nanoparticles (here Zr-based metal-organic-framework nanoparticles) with integrated cargo molecules (here organic fluorophores), with aze that does not allow for efficient exocytosis, a material which only partly degrades under acidic conditions as present in endosomes/lysosomes, and with limited colloidal stability. Data show that, for Zr-based metal-organic-framework nanoparticles of 40 nm size as investigated here, the number of nanoparticles per cells decreases faster due to particle redistribution upon proliferation than due to nanoparticle exocytosis and that, thus, also for this system, exocytosis is not an efficient pathway for clearance of the nanoparticles from the cells.

Identifiers

PMID37881592
PMCPMC10594580
OpenAlexW4386400133

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.