304
Shoubaky GAE, Abdel-Daim MM, Mansour MH, Salem EA (2016) Isolation and identification of
a flavone apigenin from marine red alga Acanthophora spicifera with antinociceptive and antiInflammatory activities. J Exp Neurosci 10:JEN.S25096. https://doi.org/10.4137/JEN.S25096
Silva LP, Fernandez L, Conceição JHF et al (2018) Design and characterization of sugar-based
Deep Eutectic Solvents using conductor-like screening model for real solvents. ACS Sustain
Chem Eng 6:10724–10734. https://doi.org/10.1021/acssuschemeng.8b02042
Singh BS, Lobo HR, Pinjari DV et al (2013) Ultrasound and deep eutectic solvent (DES): A novel
blend of techniques for rapid and energy efficient synthesis of oxazoles. Ultrason Sonochem
20:287–293. https://doi.org/10.1016/j.ultsonch.2012.06.003
Singleton VL, Orthofer R, Lamuela-Raventós RM (1999) Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Ciocalteu reagent. In: Methods in enzymology. Academic Press, Amsterdam, pp 152–178
Skulcova A, Haščičová Z, Hrdlicka L, Sima J, Jablonsky M (2018) Green Solvents based on choline chloride extraction of Spruce Bark (Picea Abies). Cellul Chem Technol 52:171–179
Swain T, Bate-Smith EC (1962) Flavonoid compounds. In: Comparative biochemistry. Academic
Press, New York
Tanase C, Coșarcă S, Muntean D-L (2019) A critical review of phenolic compounds extracted from
the bark of woody vascular plants and their potential biological activity. Molecules 24:1182.
https://doi.org/10.3390/molecules24061182
Tang B, Bi W, Tian M, Row KH (2012) Application of ionic liquid for extraction and separation of bioactive compounds from plants. J Chromatogr B 904:1–21. https://doi.org/10.1016/j.
jchromb.2012.07.020
Tang B, Park HE, Row KH (2015) Simultaneous extraction of flavonoids from Chamaecyparis
obtusa using Deep Eutectic Solvents as additives of conventional extractions solvents. J
Chromatogr Sci 53:836–840. https://doi.org/10.1093/chromsci/bmu108
Tang W, Li G, Chen B et al (2017) Evaluating ternary deep eutectic solvents as novel media for
extraction of flavonoids from Ginkgo biloba. Sep Sci Technol 52:91–99. https://doi.org/10.108
0/01496395.2016.1247864
Tanna B, Mishra A (2018) Metabolites unravel nutraceutical potential of edible seaweeds: an
emerging source of functional food. Compr Rev Food Sci Food Saf 17:1613–1624. https://doi.
org/10.1111/1541-4337.12396
Tian H, Wang J, Li Y et al (2019) Recovery of natural products from Deep Eutectic Solvents
by mimicking denaturation. ACS Sustain Chem Eng 7:9976–9983. https://doi.org/10.1021/
acssuschemeng.9b01012
Tiwari BK (2015) Ultrasound: a clean, green extraction technology. TrAC Trends Anal Chem
71:100–109. https://doi.org/10.1016/j.trac.2015.04.013
Treutter D (2006) Significance of flavonoids in plant resistance: a review. Environ Chem Lett
4:147–157. https://doi.org/10.1007/s10311-006-0068-8
Tsao R (2010) Chemistry and biochemistry of dietary polyphenols. Nutrients 2:1231–1246.
https://doi.org/10.3390/nu2121231
van Osch DJGP, Parmentier D, Dietz CHJT et al (2016) Removal of alkali and transition metal ions
from water with hydrophobic deep eutectic solvents. Chem Commun 52:11987–11990. https://
doi.org/10.1039/C6CC06105B
Vanda H, Dai Y, Wilson EG et al (2018) Green solvents from ionic liquids and deep eutectic
solvents to natural deep eutectic solvents. Comptes Rendus Chim 21:628–638. https://doi.
org/10.1016/j.crci.2018.04.002
Vaya J, Mahmood S, Goldblum A et al (2003) Inhibition of LDL oxidation by flavonoids in relation
to their structure and calculated enthalpy. Phytochemistry 62:89–99. https://doi.org/10.1016/
S0031-9422(02)00445-4
Velmurugan BK, Rathinasamy B, Lohanathan BP et al (2018) Neuroprotective role of phytochemicals. Molecules 23:2485
L. Percevault et al.
Shoubaky GAE, Abdel-Daim MM, Mansour MH, Salem EA (2016) Isolation and identification of
a flavone apigenin from marine red alga Acanthophora spicifera with antinociceptive and antiInflammatory activities. J Exp Neurosci 10:JEN.S25096. https://doi.org/10.4137/JEN.S25096
Silva LP, Fernandez L, Conceição JHF et al (2018) Design and characterization of sugar-based
Deep Eutectic Solvents using conductor-like screening model for real solvents. ACS Sustain
Chem Eng 6:10724–10734. https://doi.org/10.1021/acssuschemeng.8b02042
Singh BS, Lobo HR, Pinjari DV et al (2013) Ultrasound and deep eutectic solvent (DES): A novel
blend of techniques for rapid and energy efficient synthesis of oxazoles. Ultrason Sonochem
20:287–293. https://doi.org/10.1016/j.ultsonch.2012.06.003
Singleton VL, Orthofer R, Lamuela-Raventós RM (1999) Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Ciocalteu reagent. In: Methods in enzymology. Academic Press, Amsterdam, pp 152–178
Skulcova A, Haščičová Z, Hrdlicka L, Sima J, Jablonsky M (2018) Green Solvents based on choline chloride extraction of Spruce Bark (Picea Abies). Cellul Chem Technol 52:171–179
Swain T, Bate-Smith EC (1962) Flavonoid compounds. In: Comparative biochemistry. Academic
Press, New York
Tanase C, Coșarcă S, Muntean D-L (2019) A critical review of phenolic compounds extracted from
the bark of woody vascular plants and their potential biological activity. Molecules 24:1182.
https://doi.org/10.3390/molecules24061182
Tang B, Bi W, Tian M, Row KH (2012) Application of ionic liquid for extraction and separation of bioactive compounds from plants. J Chromatogr B 904:1–21. https://doi.org/10.1016/j.
jchromb.2012.07.020
Tang B, Park HE, Row KH (2015) Simultaneous extraction of flavonoids from Chamaecyparis
obtusa using Deep Eutectic Solvents as additives of conventional extractions solvents. J
Chromatogr Sci 53:836–840. https://doi.org/10.1093/chromsci/bmu108
Tang W, Li G, Chen B et al (2017) Evaluating ternary deep eutectic solvents as novel media for
extraction of flavonoids from Ginkgo biloba. Sep Sci Technol 52:91–99. https://doi.org/10.108
0/01496395.2016.1247864
Tanna B, Mishra A (2018) Metabolites unravel nutraceutical potential of edible seaweeds: an
emerging source of functional food. Compr Rev Food Sci Food Saf 17:1613–1624. https://doi.
org/10.1111/1541-4337.12396
Tian H, Wang J, Li Y et al (2019) Recovery of natural products from Deep Eutectic Solvents
by mimicking denaturation. ACS Sustain Chem Eng 7:9976–9983. https://doi.org/10.1021/
acssuschemeng.9b01012
Tiwari BK (2015) Ultrasound: a clean, green extraction technology. TrAC Trends Anal Chem
71:100–109. https://doi.org/10.1016/j.trac.2015.04.013
Treutter D (2006) Significance of flavonoids in plant resistance: a review. Environ Chem Lett
4:147–157. https://doi.org/10.1007/s10311-006-0068-8
Tsao R (2010) Chemistry and biochemistry of dietary polyphenols. Nutrients 2:1231–1246.
https://doi.org/10.3390/nu2121231
van Osch DJGP, Parmentier D, Dietz CHJT et al (2016) Removal of alkali and transition metal ions
from water with hydrophobic deep eutectic solvents. Chem Commun 52:11987–11990. https://
doi.org/10.1039/C6CC06105B
Vanda H, Dai Y, Wilson EG et al (2018) Green solvents from ionic liquids and deep eutectic
solvents to natural deep eutectic solvents. Comptes Rendus Chim 21:628–638. https://doi.
org/10.1016/j.crci.2018.04.002
Vaya J, Mahmood S, Goldblum A et al (2003) Inhibition of LDL oxidation by flavonoids in relation
to their structure and calculated enthalpy. Phytochemistry 62:89–99. https://doi.org/10.1016/
S0031-9422(02)00445-4
Velmurugan BK, Rathinasamy B, Lohanathan BP et al (2018) Neuroprotective role of phytochemicals. Molecules 23:2485
L. Percevault et al.