Journal of Pharmaceutical Analysis · 2021 · 25 citations · 39 references
PharmacyMedicinal ChemistryDrug DiscoveryPharmaceutical RheologySeparation ScienceExtraction TechniquesMetabolite ExtractionSafer SolventsSolvent ExtractionDeep Eutectic Solvent ExtractionDeep Eutectic Solvent SynthesisDeep Eutectic SolventsExtraction Of Organic CompoundsExtraction SolventsExtraction YieldNatural Product ExtractionViscosity
Natural long-chain alkanol and alkyl carboxylic acid were used to prepare novel hydrophobic deep eutectic solvents (HDESs). These HDESs are liquid at room temperature and have low viscosity (<12.26 mPa‧s), low polarity (lower than that of methanol, ChCl-based deep eutectic solvents and other reported HDESs), and low density (<0.928 g/mL). A simple one-pot method based on a novel HDES–water two-phase extraction system was constructed for the extraction of weak-polarity bioactive components, anthraquinones, from Rhei Radix et Rhizoma. This HDES-based new extraction method does not consume hazardous organic solvents and can obtain a total anthraquinone yield of 21.52 mg/g, which is close to that obtained by the Chinese pharmacopoeia method (21.22 mg/g) and considerably higher than those by other reported HDESs-based extraction methods (14.20–20.09 mg/g, p < 0.01). The high extraction yield can be mainly attributed to the severe destruction of the RRR cell walls by the extraction system and the excellent dissolving ability of novel HDESs for anthraquinones.
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Ullmann's Encyclopedia of Industrial Chemistry
Choice Reviews Online · 2012 · 3.1K citations
Natural deep eutectic solvents as new potential media for green technology
Yuntao Dai, Jaap van Spronsen, Geert‐Jan Witkamp et al. · Analytica Chimica Acta · 2013 · 2.6K citations · Full text