Literature DB >> 28389917

A green analytical chemistry approach for lipid extraction: computation methods in the selection of green solvents as alternative to hexane.

Mari Merce Cascant1,2, Cassandra Breil1, Salvador Garrigues2, Miguel de la Guardia3, Anne Silvie Fabiano-Tixier1, Farid Chemat4.   

Abstract

There is a great interest in finding alternatives and green solvents in extraction processes to replace petroleum based solvents. In order to investigate these possibilities, computational methods, as Hansen solubility parameters (HSP) and conductor-like screening model for real solvent (COSMO-RS), were used in this work to predict the solvation power of a series of solvents in salmon fish lipids. Additionally, experimental studies were used to evaluate the performance in lipids extraction using 2-methyltetrahydrofurane, cyclopentyl methyl ether, dimethyl carbonate, isopropanol, ethanol, ethyl acetate, p-cymene and d-limonene compared with hexane. Lipid classes of extracts were obtained by using high performance thin-layer chromatography (HPTLC), whereas gas chromatography with a flame ionization detector (GC/FID) technique was employed to obtain fatty acid profiles. Some differences between theoretical and experimental results were observed, especially regarding the behavior of p-cymene and d-limonene, which separate from the predicted capability. Results obtained from HPTLC indicated that p-cymene and d-limonene extract triglycerides (TAGs) and diglycerides (DAGs) at levels of 73 and 19%, respectively, whereas the other studied extracts contain between 75 and 76% of TAGs and between 16 and 17% of DAGs. Fatty acid profiles, obtained by using GC-FID, indicated that saturated fatty acids (SFAs) between 19.5 and 19.9% of extracted oil, monounsaturated fatty acids (MUFAs) in the range between 43.5 and 44.9%, and PUFAs between 31.2 and 34.6% were extracted. p-Cymene and limonene extracts contained lower percentages than the other studied solvents of some PUFAs due probably to the fact that these unsaturated fatty acids are more susceptible to oxidative degradation than MUFAs. Ethyl acetate has been found to be the best alternative solvent to hexane for the extraction of salmon oil lipids. Graphical Abstract ᅟ.

Entities:  

Keywords:  Cosmo-RS; Green alternative solvent; Hansen parameters; Lipid extraction; Salmon fish; n-Hexane

Mesh:

Substances:

Year:  2017        PMID: 28389917     DOI: 10.1007/s00216-017-0323-9

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  5 in total

1.  Omega-3 Extraction from Anchovy Fillet Leftovers with Limonene: Chemical, Economic, and Technical Aspects.

Authors:  Rosaria Ciriminna; Antonino Scurria; Anne-Sylvie Fabiano-Tixier; Claudia Lino; Giuseppe Avellone; Farid Chemat; Mario Pagliaro
Journal:  ACS Omega       Date:  2019-09-12

2.  para-Menthane as a Stable Terpene Derived from Orange By-Products as a Novel Solvent for Green Extraction and Solubilization of Natural Substances.

Authors:  Sara Madji; Soukaina Hilali; Anne-Sylvie Fabiano-Tixier; Mathieu Tenon; Antoine Bily; Mickaël Laguerre; Farid Chemat
Journal:  Molecules       Date:  2019-06-09       Impact factor: 4.411

3.  Pressurized natural deep eutectic solvents: An alternative approach to agro-soy by-products.

Authors:  Felipe Sanchez Bragagnolo; Bárbara Socas-Rodríguez; Jose A Mendiola; Alejandro Cifuentes; Cristiano Soleo Funari; Elena Ibáñez
Journal:  Front Nutr       Date:  2022-09-08

4.  2-Methyloxolane as a Bio-Based Solvent for Green Extraction of Aromas from Hops (Humulus lupulus L.).

Authors:  Vincent Rapinel; Aziadé Chemat; Cyrille Santerre; Justine Belay; Farnaz Hanaei; Nadine Vallet; Laurence Jacques; Anne-Sylvie Fabiano-Tixier
Journal:  Molecules       Date:  2020-04-09       Impact factor: 4.411

Review 5.  2-Methyloxolane (2-MeOx) as Sustainable Lipophilic Solvent to Substitute Hexane for Green Extraction of Natural Products. Properties, Applications, and Perspectives.

Authors:  Vincent Rapinel; Ombéline Claux; Maryline Abert-Vian; Christine McAlinden; Mickael Bartier; Norbert Patouillard; Laurence Jacques; Farid Chemat
Journal:  Molecules       Date:  2020-07-28       Impact factor: 4.411

  5 in total

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