Evidence map›Paper›PMID 36619665›Full record

ArticleJournal of the American Oil Chemists' Society2022

Exploring how changes to the steroidal core alter oleogelation capability in sterol: γ-oryzanol blends.

Andrew B Matheson, Georgios Dalkas, Gareth O Lloyd, Aaliyah Hart, Arjen Bot, Ruud den Adel, Vasileios Koutsos, Paul S Clegg, Stephen R Euston

Abstract read
In one paragraph

Article in Journal of the American Oil Chemists' Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Andrew B MathesonSchool of Physics and Astronomy University of Edinburgh Edinburgh UK.ORCID https://orcid.org/0000-0002-9391-6469
Georgios DalkasSchool of Engineering and Physical Sciences, Institute of Biological Chemistry, Biophysics and Bioengineering Heriot-Watt University Edinburgh UK.ORCID https://orcid.org/0000-0003-2628-047X
Gareth O LloydSchool of Chemistry, Joseph Banks Laboratories University of Lincoln Lincoln UK.ORCID https://orcid.org/0000-0002-1013-1480
Aaliyah HartSchool of Chemistry, Joseph Banks Laboratories University of Lincoln Lincoln UK.
Arjen BotUnilever Foods Innovation Centre Wageningen The Netherlands.ORCID https://orcid.org/0000-0002-2065-8964
Ruud den AdelUnilever Foods Innovation Centre Wageningen The Netherlands.ORCID https://orcid.org/0000-0003-3306-2614
Vasileios KoutsosSchool of Engineering, Institute for Materials and Processes The University of Edinburgh Edinburgh UK.ORCID https://orcid.org/0000-0002-2203-8179
Paul S CleggSchool of Physics and Astronomy University of Edinburgh Edinburgh UK.ORCID https://orcid.org/0000-0003-0280-4670
Stephen R EustonSchool of Engineering and Physical Sciences, Institute of Biological Chemistry, Biophysics and Bioengineering Heriot-Watt University Edinburgh UK.ORCID https://orcid.org/0000-0003-1869-6846

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oleogels based on sterols such as β-sitosterol blended with the sterol ester γ-oryzanol are a very interesting class of systems, but there are aspects of their formation and structure that remain elusive. It has previously been shown that a methyl group on the C30 position of the sterol-ester plays an important role in gelation. This work explored the effect that having C30 methyl groups on both the sterol and the sterol-ester had on the gelation process and subsequent gel structure. Lanosterol and saponified γ-oryzanol (which was synthesized as part of this study) were identified as materials of interest, as both feature a methyl group on the C30 position of their steroidal cores. It was observed that both sterols formed gels when blended with γ-oryzanol, and also that lanosterol gelled sunflower oil without the addition of γ-oryzanol. All of these gels were significantly weaker than that formed by β-sitosterol blended with γ-oryzanol. To explore why, molecular docking simulations along with AFM and SAXS were used to examine these gels on a broad range of length scales. The results suggest that saponified γ-oryzanol-γ-oryzanol gels have a very similar structure to that of β-sitosterol-γ-oryzanol gels. Lanosterol-γ-oryzanol gels and pure lanosterol gel, however, form with a totally different structure facilitated by the head-to-tail stacking motif exhibited by lanosterol. These results give further evidence that relatively slight changes to the molecular structure of gelators can result in significant differences in subsequent gel properties.

Indexed as

fat substitutesnutraceuticals/functional foodsrheologystructure–functional properties

Identifiers

PMID36619665
PMCPMC9796822

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.