Evidence map›Paper›PMID 35539117›Full record

ArticleRSC advances2018

Surface-grafted polyethylene glycol conformation impacts the transport of PEG-functionalized liposomes through a tumour extracellular matrix model.

Hagar I Labouta, M Juliana Gomez-Garcia, Christopher D Sarsons, Trinh Nguyen, Jacob Kennard, Wayne Ngo, Kaisha Terefe, Nicolas Iragorri, Patrick Lai, Kristina D Rinker and 1 more

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Polymerization from Lipid Membranes.Biomacromolecules · 2026
    Article
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  19. Article
  20. Building Blocks to Design Liposomal Delivery Systems.International journal of molecular sciences · 2020
    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

11 authors at 1 institution in 2 countries.

Hagar I LaboutaDepartment of Chemistry, Faculty of Science, University of Calgary Canada dcramb@ucalgary.ca.
M Juliana Gomez-GarciaBiomedical Engineering, University of Calgary Canada kdrinker@ucalgary.ca.
Christopher D SarsonsBiomedical Engineering, University of Calgary Canada kdrinker@ucalgary.ca.
Trinh NguyenDepartment of Chemistry, Faculty of Science, University of Calgary Canada dcramb@ucalgary.ca.
Jacob KennardBiomedical Engineering, University of Calgary Canada kdrinker@ucalgary.ca.
Wayne NgoDepartment of Chemistry, Faculty of Science, University of Calgary Canada dcramb@ucalgary.ca.
Kaisha TerefeBiomedical Engineering, University of Calgary Canada kdrinker@ucalgary.ca.
Nicolas IragorriHealth Technology Assessment Unit, Department of Community Health Sciences, Cumming School of Medicine, University of Calgary Canada.
Patrick LaiDepartment of Biological Sciences, University of Calgary Canada.
Kristina D RinkerBiomedical Engineering, University of Calgary Canada kdrinker@ucalgary.ca.
David T CrambDepartment of Chemistry, Faculty of Science, University of Calgary Canada dcramb@ucalgary.ca.ORCID https://orcid.org/0000-0003-2494-0091
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effect of surface PEGylation on nanoparticle transport through an extracellular matrix (ECM) is an important determinant for tumor targeting success. Fluorescent stealth liposomes (base lipid DOPC) were prepared incorporating different proportions of PEG-grafted lipids (2.5, 5 and 10% of the total lipid content) for a series of PEG molecular weights (1000, 2000 and 5000 Da). The ECM was modelled using a collagen matrix. The kinetics of PEGylated liposome adhesion to and transport in collagen matrices were tracked using fluorescence correlation spectroscopy (FCS) and confocal microscopy, respectively. Generalized least square regressions were used to determine the temporal correlations between PEG molecular weight, surface density and conformation, and the liposome transport in a collagen hydrogel over 15 hours. PEG conformation determined the interaction of liposomes with the collagen hydrogel and their transport behaviour. Interestingly, liposomes with mushroom PEG conformation accumulated on the interface of the collagen hydrogel, creating a dense liposomal front with short diffusion distances into the hydrogels. On the other hand, liposomes with dense brush PEG conformation interacted to a lesser extent with the collagen hydrogel and diffused to longer distances. In conclusion, a better understanding of PEG surface coating as a modifier of transport in a model ECM matrix has resulted. This knowledge will improve design of future liposomal drug carrier systems.

Identifiers

PMID35539117
PMCPMC9078461
OpenAlexW2787882338

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.