Chemically vs Enzymatically Synthesized Polyglycerol-Based Esters: A Comparison between Their Surfactancy.


Journal

ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658

Informations de publication

Date de publication:
25 Jul 2023
Historique:
received: 28 04 2023
accepted: 09 06 2023
medline: 31 7 2023
pubmed: 31 7 2023
entrez: 31 7 2023
Statut: epublish

Résumé

Polyglycerol fatty acid esters (PGFAEs) are gaining interest in several industrial sectors due to their excellent surfactant properties and their wide range of hydrophilic-lipophilic balance (HLB) values. Moreover, they can be prepared from renewable resources, i.e., fatty acids and glycerol. In this study, polyglycerol-2 stearic acid esters (PG2SAEs) were synthesized by the enzymatic esterification of polyglycerol-2 (PG2) and stearic acid (SA) using the immobilized lipase Novozym 435 as a biocatalyst in a solvent-free system. Reaction conditions,

Identifiants

pubmed: 37521610
doi: 10.1021/acsomega.3c02922
pmc: PMC10373213
doi:

Types de publication

Journal Article

Langues

eng

Pagination

26405-26413

Informations de copyright

© 2023 The Authors. Published by American Chemical Society.

Déclaration de conflit d'intérêts

The authors declare no competing financial interest.

Références

Chem Soc Rev. 2013 Aug 7;42(15):6475-90
pubmed: 23515487
J Agric Food Chem. 2018 Aug 1;66(30):8104-8113
pubmed: 29989410
Chem Rev. 2010 Mar 10;110(3):1807
pubmed: 20184346
J Colloid Interface Sci. 2000 Oct 1;230(1):213-215
pubmed: 10998309
Appl Biochem Biotechnol. 2016 Jun;179(3):485-96
pubmed: 26883757
Chempluschem. 2023 Jan;88(1):e202200331
pubmed: 36592040
J Biosci Bioeng. 2003;95(5):466-9
pubmed: 16233441
Appl Biochem Biotechnol. 2004 Jul-Sep;118(1-3):155-70
pubmed: 15304746
Biotechnol J. 2018 Jun;13(6):e1700629
pubmed: 29542861
Microb Cell Fact. 2020 Aug 26;19(1):169
pubmed: 32847584
J Lipid Res. 2015 Dec;56(12):2348-58
pubmed: 26447231
Indian J Biochem Biophys. 2013 Dec;50(6):570-6
pubmed: 24772983
Chem Soc Rev. 2013 Aug 7;42(15):6437-74
pubmed: 23436023

Auteurs

Jacopo F A A Amari (JFAA)

Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.

Sara Sangiorgio (S)

Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.

Eleonora Pargoletti (E)

Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.

Marco Rabuffetti (M)

Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.

Federica Zaccheria (F)

CNR, Istituto di Scienze e Tecnologie Chimiche "G. Natta" (SCITEC), Via Golgi 19, 20133 Milan, Italy.

Fabio Usuelli (F)

Res Novare S.r.l., via Italia 197, Int.10 c/o Centro comm. Globo, 20874 Busnago, Italy.

Valeria Quaranta (V)

Res Novare S.r.l., via Italia 197, Int.10 c/o Centro comm. Globo, 20874 Busnago, Italy.

Giovanna Speranza (G)

Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.

Giuseppe Cappelletti (G)

Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.

Classifications MeSH