Evidence map›Paper›PMID 35061359›Full record

ArticleBiomacromolecules2022

Fluorescence Correlation Spectroscopy Monitors the Fate of Degradable Nanocarriers in the Blood Stream.

Sascha Schmitt, Anne Huppertsberg, Adrian Klefenz, Leonard Kaps, Volker Mailänder, Detlef Schuppan, Hans-Jürgen Butt, Lutz Nuhn, Kaloian Koynov

Open access · hybridAbstract read
In one paragraph

Article in Biomacromolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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  11. pH-degradable, bisphosphonate-loaded nanogels attenuate liver fibrosis by repolarization of M2-type macrophages.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

9 authors at 3 institutions in 2 countries.

Sascha SchmittMax Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
Anne HuppertsbergMax Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
Adrian KlefenzInstitute for Translational Immunology and Research Center for Immune Therapy, University Medical Center, Johannes Gutenberg University, 55131 Mainz, Germany.
Leonard KapsInstitute for Translational Immunology and Research Center for Immune Therapy, University Medical Center, Johannes Gutenberg University, 55131 Mainz, Germany.
Volker MailänderMax Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.ORCID 0000-0001-6583-8136
Detlef SchuppanInstitute for Translational Immunology and Research Center for Immune Therapy, University Medical Center, Johannes Gutenberg University, 55131 Mainz, Germany.
Hans-Jürgen ButtMax Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.ORCID 0000-0001-5391-2618
Lutz NuhnMax Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.ORCID 0000-0003-0761-1106
Kaloian KoynovMax Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.ORCID 0000-0002-4062-8834
Max Planck Institute for Polymer Research · DEJohannes Gutenberg University Mainz · DEBeth Israel Deaconess Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of nanoparticles as carriers to deliver pharmacologically active compounds to specific parts of the body via the bloodstream is a promising therapeutic approach for the effective treatment of various diseases. To reach their target sites, nanocarriers (NCs) need to circulate in the bloodstream for prolonged periods without aggregation, degradation, or cargo loss. However, it is very difficult to identify and monitor small-sized NCs and their cargo in the dense and highly complex blood environment. Here, we present a new fluorescence correlation spectroscopy-based method that allows the precise characterization of fluorescently labeled NCs in samples of less than 50 μL of whole blood. The NC size, concentration, and loading efficiency can be measured to evaluate circulation times, stability, or premature drug release. We apply the new method to follow the fate of pH-degradable fluorescent cargo-loaded nanogels in the blood of live mice for periods of up to 72 h.

Indexed as

Drug CarriersNanoparticlesAnimalsDrug LiberationMiceMicellesSpectrometry, FluorescenceDrug CarriersMicelles

Identifiers

PMID35061359
PMCPMC8924869
OpenAlexW4207018795

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.