Evidence map›Paper›PMID 30265794›Full record

ArticleBiomacromolecules2019

Development of Morphologically Discrete PEG-PDLLA Nanotubes for Precision Nanomedicine.

Annelies C Wauters, Imke A B Pijpers, Alexander F Mason, David S Williams, Jurjen Tel, Loai K E A Abdelmohsen, Jan C M van Hest

Abstract read
In one paragraph

Article in Biomacromolecules, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Medical micro- and nanomotors in the body.Acta pharmaceutica Sinica. B · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. 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

7 authors.

Annelies C WautersBio-Organic Chemistry, Institute for Complex Molecular Systems , Eindhoven University of Technology , P.O. Box 513 (STO 3.41), 5600 MB Eindhoven , The Netherlands.
Imke A B PijpersBio-Organic Chemistry, Institute for Complex Molecular Systems , Eindhoven University of Technology , P.O. Box 513 (STO 3.41), 5600 MB Eindhoven , The Netherlands.
Alexander F MasonBio-Organic Chemistry, Institute for Complex Molecular Systems , Eindhoven University of Technology , P.O. Box 513 (STO 3.41), 5600 MB Eindhoven , The Netherlands.ORCID 0000-0002-2847-0253
David S WilliamsDepartment of Chemistry, College of Science , Swansea University , Swansea , United Kingdom.ORCID 0000-0002-8209-6899
Jurjen TelDepartment of Biomedical Engineering, Laboratory of Immunoengineering , Eindhoven University of Technology , 5600 MB Eindhoven , The Netherlands.
Loai K E A AbdelmohsenBio-Organic Chemistry, Institute for Complex Molecular Systems , Eindhoven University of Technology , P.O. Box 513 (STO 3.41), 5600 MB Eindhoven , The Netherlands.ORCID 0000-0002-0094-1893
Jan C M van HestBio-Organic Chemistry, Institute for Complex Molecular Systems , Eindhoven University of Technology , P.O. Box 513 (STO 3.41), 5600 MB Eindhoven , The Netherlands.ORCID 0000-0001-7973-2404

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise control over the morphological features of nanoparticles is an important requisite for their application in nanomedical research. Parameters such as size and shape have been identified as critical features for effective nanotherapeutic technologies due to their role in circulation, distribution, and internalization in vivo. Tubular PEG-PDLLA polymersomes (nanotubes) exhibit an interesting morphology with potential for immunotherapeutics, as the elongated shape can affect cell-particle interactions. Developing methodologies that permit control over the precise form of such nanotubes is important for their biomedical implementation due to the stringent physicochemical constraints for efficacious performance. Through careful control over the engineering process, we demonstrate the generation of well-defined nanotubes based on polymersomes as small as 250 and 100 nm, which can be successfully shape transformed. The quality of the resulting nanostructures was established by physical characterization using AF4-MALS and cryo-TEM. Moreover, we show the successful loading of such nanotubes with model payloads (proteins and drugs). These findings provide a promising platform for implementation in biomedical applications in which discrete structure and functionality are essential features.

Indexed as

Drug CarriersNanomedicineNanotubesPolyethylene GlycolsPolyethyleneimineDrug CarriersPolyethylene GlycolsPolyethyleneimine

Identifiers

PMID30265794
PMCPMC6335608

What OpenQuestion holds

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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.