Evidence map›Paper›PMID 33291641›Full record

ArticleMolecules (Basel, Switzerland)2020

Phase Behavior and Polymorphism of Saturated and Unsaturated Phytosterol Esters.

Eva Daels, Imogen Foubert, Zheng Guo, Wim Thielemans, Bart Goderis

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 2 countries.

Eva DaelsResearch Unit Food and Lipids, Department of Microbial and Molecular Systems (M²S), KU Leuven, Campus Kulak Kortrijk, Etienne Sabbelaan 53 Box 7659, 8500 Kortrijk, Belgium.
Imogen FoubertResearch Unit Food and Lipids, Department of Microbial and Molecular Systems (M²S), KU Leuven, Campus Kulak Kortrijk, Etienne Sabbelaan 53 Box 7659, 8500 Kortrijk, Belgium.ORCID 0000-0001-8735-8926
Zheng GuoAgro-Biotechnology Science Lab, Department of Engineering, Aarhus University, Gustav Wieds Vej 10 building 3141, 01.18, 8000 Aarhus, Denmark.ORCID 0000-0002-8436-7082
Wim ThielemansSustainable Materials Lab, Department of Chemical Engineering, KU Leuven, Campus Kulak Kortrijk, Etienne Sabbelaan 53 Box 7659, 8500 Kortrijk, Belgium.
Bart GoderisPolymer Chemistry and Materials, Department of Chemistry, KU Leuven, Celestijnenlaan 200f Box 2404, 3001 Leuven, Belgium.ORCID 0000-0002-0807-5790
KU Leuven · BEAarhus University · DK

Funding

CRG committee 26-02-839Fonds Wetenschappelijk Onderzoek nr
6 · The paper itself

Abstract

This study investigated how the physicochemical characteristics of phytosterol esters are influenced by the chain length and degree of unsaturation of the fatty acid ester moiety. Saturated and unsaturated phytosterol esters (PEs) were synthesized by the esterification of different types of fatty acids (stearic, palmitic, lauric, oleic, and linoleic acid) to β-sitosterol. The non-isothermal crystallization and melting behavior of the pure PEs were analyzed. It was proven by X-ray diffraction that saturated β-sitosteryl esters and β-sitosteryl oleate formed a bilayer crystal structure. The lamellar spacings of the bilayer structure decreased with decreasing fatty acid chain length and with an increasing degree in unsaturation. The degree of unsaturation of the fatty acid chain of the β-sitosteryl esters also influenced the type of subcell packing of the fatty acid moieties in the bilayer structure, whether or not a metastable or stable liquid crystalline phase was formed during cooling. Furthermore, it was found that the melting temperature and enthalpy of the β-sitosteryl esters increased with an increasing fatty acid chain length while they decreased with an increasing degree of unsaturation. The microscopic analyses demonstrated that β-sitosteryl oleate formed much smaller spherulites than their saturated β-sitosteryl analogues.

Indexed as

CrystallizationEstersFatty AcidsPhytosterolsSitosterolsTemperatureX-Ray DiffractionEstersFatty AcidsPhytosterolsSitosterolslipid crystallizationmelting behaviorphytosterol esterspolymorphismsynchrotron X-ray diffraction

Identifiers

PMID33291641
PMCPMC7729458
OpenAlexW3108288526

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.