Evidence map›Paper›PMID 25383302›Full record

ArticleBeilstein journal of nanotechnology2014

Imaging the intracellular degradation of biodegradable polymer nanoparticles.

Anne-Kathrin Barthel, Martin Dass, Melanie Dröge, Jens-Michael Cramer, Daniela Baumann, Markus Urban, Katharina Landfester, Volker Mailänder, Ingo Lieberwirth

Abstract read
In one paragraph

Article in Beilstein journal of nanotechnology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  6. Review
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.

Anne-Kathrin BarthelMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Martin DassMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Melanie DrögeMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Jens-Michael CramerMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Daniela BaumannMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Markus UrbanMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Katharina LandfesterMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.
Volker MailänderMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany ; 3rd Department of Medicine (Hematology, Oncology, and Pneumology), University Medical Center of the Johannes Gutenberg-University Mainz, Langenbeckstraße 1, 55131 Mainz, Germany.
Ingo LieberwirthMax-Planck-Institute for Polymer Research, Ackermannweg 10, 55123 Mainz, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, the development of smart drug delivery systems based on biodegradable polymeric nanoparticles has become of great interest. Drug-loaded nanoparticles can be introduced into the cell interior via endocytotic processes followed by the slow release of the drug due to degradation of the nanoparticle. In this work, poly(L-lactic acid) (PLLA) was chosen as the biodegradable polymer. Although common degradation of PLLA has been studied in various biological environments, intracellular degradation processes have been examined only to a very limited extent. PLLA nanoparticles with an average diameter of approximately 120 nm were decorated with magnetite nanocrystals and introduced into mesenchymal stem cells (MSCs). The release of the magnetite particles from the surface of the PLLA nanoparticles during the intracellular residence was monitored by transmission electron microscopy (TEM) over a period of 14 days. It was demonstrated by the release of the magnetite nanocrystals from the PLLA surface that the PLLA nanoparticles do in fact undergo degradation within the cell. Furthermore, even after 14 days of residence, the PLLA nanoparticles were found in the MSCs. Additionally, the ultrastructural TEM examinations yield insight into the long term intercellular fate of these nanoparticles. From the statistical analysis of ultrastructural details (e.g., number of detached magnetite crystals, and the number of nanoparticles in one endosome), we demonstrate the importance of TEM studies for such applications in addition to fluorescence studies (flow cytometry and confocal laser scanning microscopy).

Indexed as

biodegradationmesenchymal stem cellsPLLA nanoparticlestransmission electron microscopy

Identifiers

PMID25383302
PMCPMC4222285

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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.