Evidence map›Paper›PMID 30789270›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2019

Shape and Phase Transitions in a PEGylated Phospholipid System.

Lauri Viitala, Saija Pajari, Luigi Gentile, Jukka Määttä, Marta Gubitosi, Jan Deska, Maria Sammalkorpi, Ulf Olsson, Lasse Murtomäki

Open access · hybridAbstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  6. Charge-Stabilized Nanodiscs as a New Class of Lipid Nanoparticles.Advanced materials (Deerfield Beach, Fla.) · 2024
    Article
  7. Article
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  9. Article
  10. α-Synuclein Interaction with Lipid Bilayer Discs.Langmuir : the ACS journal of surfaces and colloids · 2022
    Article
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  12. Review
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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 2 institutions in 3 countries.

Lauri ViitalaDepartment of Chemistry and Materials Science , Aalto University , P.O. Box 16100, FI-00076 Aalto , Finland.ORCID 0000-0002-2734-372X
Saija PajariDepartment of Chemistry and Materials Science , Aalto University , P.O. Box 16100, FI-00076 Aalto , Finland.
Luigi GentilePhysical Chemistry , Lund University , P.O. Box 124, SE-221 00 Lund , Sweden.ORCID 0000-0001-6854-2963
Jukka MäättäDepartment of Chemistry and Materials Science , Aalto University , P.O. Box 16100, FI-00076 Aalto , Finland.
Marta GubitosiPhysical Chemistry , Lund University , P.O. Box 124, SE-221 00 Lund , Sweden.
Jan DeskaDepartment of Chemistry and Materials Science , Aalto University , P.O. Box 16100, FI-00076 Aalto , Finland.
Maria SammalkorpiDepartment of Chemistry and Materials Science , Aalto University , P.O. Box 16100, FI-00076 Aalto , Finland.ORCID 0000-0002-9248-430X
Ulf OlssonPhysical Chemistry , Lund University , P.O. Box 124, SE-221 00 Lund , Sweden.ORCID 0000-0003-2200-1605
Lasse MurtomäkiDepartment of Chemistry and Materials Science , Aalto University , P.O. Box 16100, FI-00076 Aalto , Finland.ORCID 0000-0001-7667-4325
Aalto University · FILund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poly(ethylene glycol) (PEG) polymers and PEG-conjugated lipids are widely used in bioengineering and drug transport applications. A PEG layer in a drug carrier increases hydrophilic repulsion, inhibits membrane fusion and serum opsonin interactions, and prolongs the storage and circulation time. It can also change the carrier shape and have an influence on many properties related to the content release of the carrier. In this paper, we focus on the physicochemical effects of PEGylation in the lipid bilayer. We introduce laurdanC as a fluorophore for shape recognition and phase transition detection. Together with laurdanC, cryogenic transmission electron microscopy, differential scanning calorimetry, molecular dynamics simulations, and small-angle X-ray scattering/wide-angle X-ray scattering, we acquire information of the particle/bilayer morphology and phase behavior in systems containing 1,2-dipalmitoyl- sn-glycero-3-phosphocholine:1,2-distearoyl- sn-glycero-3-phosphoethanolamine-PEG(2000) with different fractions. We find that PEGylation leads to two important and potentially usable features of the system. (1) Spherical vesicles present a window of elevated chain-melting temperatures and (2) lipid packing shape-controlled liposome-to-bicelle transition. The first finding is significant for targets requiring multiple release sequences and the second enables tuning the release by composition and the PEG polymer length. Besides drug delivery systems, the findings can be used in other smart soft materials with trigger-polymers as well.

Identifiers

PMID30789270
PMCPMC6727609
OpenAlexW2915687149

What OpenQuestion holds

Textmetadata
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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.