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Alcohol Based-Deep Eutectic Solvent (DES) as an Alternative Green Additive to Increase Rotenone Yield

机译:基于醇的深层共晶溶剂(DES)作为替代绿色添加剂,以增加旋转酮产率

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Deep eutectic solvents (DESs) are basically molten salts that interact by forming hydrogen bonds between two added components at a ratio where eutectic point reaches a melting point lower than that of each individual component. Their remarkable physicochemical properties (similar to ionic liquids) with remarkable green properties, low cost and easy handling make them a growing interest in many fields of research. Therefore, the objective of pursuing this study is to analyze the potential of alcohol-based DES as an extraction medium for rotenone extraction from Derris elliptica roots. DES was prepared by a combination of choline chloride, ChCl and 1, 4-butanediol at a ratio of 1/5. The structure of elucidation of DES was analyzed using FTIR, ~1H-NMR and ~(13)C-NMR. Normal soaking extraction (NSE) method was carried out for 14 hours using seven different types of solvent systems of (1) acetone; (2) methanol; (3) acetonitrile; (4) DES; (5) DES + methanol; (6) DES + acetonitrile; and (7) [BMIM] OTf+ acetone. Next, the yield of rotenone, % (w/w), and its concentration (mg/ml) in dried roots were quantitatively determined by means of RP-HPLC. The results showed that a binary solvent system of [BMIM] OTf + acetone and DES +acetonitrile was the best solvent system combination as compared to other solvent systems. It contributed to the highest rotenone content of 0.84 ± 0.05% (w/w) (1.09 ± 0.06 mg/ml) and 0.84 ± 0.02% (w/w) (1.03 ± 0.01 mg/ml) after 14 hours of exhaustive extraction time. In conclusion, a combination of the DES with a selective organic solvent has been proven to have a similar potential and efficiency as of ILs in extracting bioactive constituents in the phytochemical extraction process.
机译:深度共晶溶剂(DESS)是基本上熔融的盐,其通过以共晶点达到低于每种组分的熔点的比例在两个添加的组分之间形成氢键。它们具有显着的物理化学性质(类似于离子液体),具有显着的绿色特性,低成本和易于处理使其成为许多研究领域的兴趣。因此,追求本研究的目的是分析醇类的潜力作为来自达氏椭葱根根的Rotenone提取的萃取介质。通过氯化胆碱,CHCl和1,4-丁二醇的组合以1/5的比例来制备。使用FTIR,〜1H-NMR和〜(13)C-NMR分析DE释放结构。使用七种不同类型的(1)丙酮的溶剂系统进行常规浸泡萃取(NSE)方法14小时; (2)甲醇; (3)乙腈; (4)des; (5)DES +甲醇; (6)DES +乙腈; (7)[BMIM] OTF +丙酮。接下来,通过RP-HPLC定量测定干燥根中旋转酮,%(w / w)及其浓度(mg / ml)的产率。结果表明,与其他溶剂系统相比,[BMIM] OTF +丙酮和DES +乙腈的二元溶剂系统是最好的溶剂系统组合。在14小时的详尽提取时间后,它导致0.84±0.05%(W / W)(1.09±0.06mg / ml)和0.84±0.02%(W ​​/ W)(1.03±0.01mg / ml)的最高旋转晶含量为0.84±0.02%(1.03±0.01mg / ml) 。总之,已被证明具有选择性有机溶剂的DE与选择性有机溶剂的组合具有与ILS在植物化学提取过程中提取生物活性成分时的类似潜在和效率。

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