Evidence map›Paper›PMID 30357152›Full record

ArticleBiomaterials science2018

Trichain cationic lipids: the potential of their lipoplexes for gene delivery.

Laila Kudsiova, Atefeh Mohammadi, M Firouz Mohd Mustapa, Frederick Campbell, Katharina Welser, Danielle Vlaho, Harriet Story, David J Barlow, Alethea B Tabor, Helen C Hailes and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Biomaterials science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  4. A review of the tortuous path of nonviral gene delivery and recent progress.International journal of biological macromolecules · 2021
    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

11 authors at 2 institutions in 3 countries.

Laila KudsiovaInstitute of Pharmaceutical Sciences. Faculty of Life Sciences and Medicine, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NH, UK.
Atefeh MohammadiDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.
M Firouz Mohd MustapaDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.
Frederick CampbellDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.
Katharina WelserDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.
Danielle VlahoDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.
Harriet StoryDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.
David J BarlowInstitute of Pharmaceutical Sciences. Faculty of Life Sciences and Medicine, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NH, UK.ORCID http://orcid.org/0000-0002-0094-5122
Alethea B TaborDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.ORCID http://orcid.org/0000-0001-8216-0347
Helen C HailesDepartment of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK. h.c.hailes@ucl.ac.uk.ORCID http://orcid.org/0000-0001-5574-4742
M Jayne LawrenceInstitute of Pharmaceutical Sciences. Faculty of Life Sciences and Medicine, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NH, UK and Division of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, Stopford Building, University of Manchester, Oxford Road, Manchester, M13 9PT, UK. jayne.lawrence@manchester.ac.uk.ORCID http://orcid.org/0000-0003-4738-4841
University College London · GBKing's College London · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/B/03645
6 · The paper itself

Abstract

Lipoplexes (LDs) have been prepared from DNA and positively charged vesicles composed of the helper lipid, dioleoyl l-α-phosphatidylethanolamine (DOPE) and either a dichain (DC) oxyethylated cationic lipid or their corresponding novel trichain (TC) counterpart. This is the first study using the TC lipids for the preparation of LDs and their application. Here the results of biophysical experiments characterising the LDs have been correlated with the in vitro transfection activity of the complexes. Photon correlation spectroscopy, zeta potential measurements and transmission electron microscopy studies indicated that, regardless of the presence of a third chain, there were little differences between the size and charge of the TC and DC containing LDs. Small angle neutron scattering studies established however that there was a significant conformational re-arrangement of the lipid bilayer when in the form of a LD complex as opposed to the parent vesicles. This re-arrangement was particularly noticeable in LDs containing TC lipids possessing a third chain of C12 or a longer chain. These results suggested that the presence of a third hydrophobic chain had a significant effect on lipid packing in the presence of DNA. Picogreen fluorescence and gel electrophoresis studies showed that the TC lipids containing a third acyl chain of at least C12 were most effective at complexing DNA while the TC lipids containing an octanoyl chain and the DC lipids were least effective. The transfection efficacies of the TC lipids in the form of LDs were found to be higher than for the DC analogues, particularly when the third acyl chain was an octanoyl or oleoyl moeity. Little or no increase in transfection efficiency was observed when the third chain was a methyl, acetyl or dodecanoyl group. The large enhancement in transfection performance of the TC lipids can be attributed to their ability to complex their DNA payload. These studies indicate that presence of a medium or long third acyl chain was especially beneficial for transfection.

Indexed as

Gene Transfer TechniquesAnimalsCationsCell LineDNALipidsLiposomesPhosphatidylethanolaminesPlasmidsRatsTransfection1,2-dielaidoylphosphatidylethanolamineCationsDNALipidsLiposomesPhosphatidylethanolamines

Identifiers

PMID30357152
PMCPMC6336150
OpenAlexW2898109973

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.