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采用乳酸乙酯提取姜黄素及其响应面法优化。

Extraction of curcuminoids by using ethyl lactate and its optimisation by response surface methodology.

机构信息

Dipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell'Aquila, Via Vetoio, 67100 Coppito, L'Aquila, Italy.

Hortus Novus, Via Aldo Moro 28 D, 67100 L'Aquila, Italy.

出版信息

J Pharm Biomed Anal. 2018 Feb 5;149:89-95. doi: 10.1016/j.jpba.2017.10.042. Epub 2017 Nov 1.

DOI:10.1016/j.jpba.2017.10.042
PMID:29102796
Abstract

Response surface methodology (RSM) was applied to optimise the extraction of curcuminoids (curcumin, demethoxycurcumin and bisdemethoxycurcumin) from turmeric using ethyl lactate (EL), ethanol and water under mild conditions (magnetic stirring at room temperature). An augmented simplex-centroid mixture design was used to monitor the dependence of the extraction efficiency from the proportions of the three solvents in the extraction medium. HPLC was used to establish the content of curcuminoids in turmeric and in the extracts. Surface plots for the extracted amount of each curcuminoid covering the whole composition domain were generated by interpolation of the experimental data with quadratic canonical polynomial models. The response surfaces of the three curcuminoids are qualitatively similar and the maximum extraction efficiency was obtained with water-EL 30:70v/v that ensured the almost quantitative recovery of the three compounds from turmeric. While degradation of the three curcuminoids in water at moderate alkaline pH is relatively fast (half-times are between 0.23 and 8.5h at pH=8.6), their stability is noticeably greater in EL (half-times are within 21-69days). Addition of EL to water is also able to inhibit the alkaline hydrolysis of curcumin and its derivatives, their half-times in the water-EL 30:70v/v, being within 40-70h at pH=8.6. The above evidences suggest that EL is a promising solvent for the extraction of curcuminods from turmeric and a suitable medium for vehiculation of these compounds into drugs or foods.

摘要

响应面法(RSM)被应用于优化姜黄中姜黄素(姜黄素、脱甲氧基姜黄素和双脱甲氧基姜黄素)的提取,使用乳酸乙酯(EL)、乙醇和水在温和条件下(室温下磁力搅拌)。采用扩充单纯形质心法混合设计来监测从萃取介质中三种溶剂的比例对萃取效率的依赖性。HPLC 用于建立姜黄和提取物中姜黄素的含量。通过用二次典型多项式模型对实验数据进行插值,生成了涵盖整个组成域的每种姜黄素提取量的表面图。三种姜黄素的响应面定性相似,水-EL30:70v/v 的最大提取效率确保了三种化合物从姜黄中几乎定量回收。虽然三种姜黄素在中等碱性 pH 下水解相对较快(pH=8.6 时半衰期在 0.23 到 8.5h 之间),但它们在 EL 中的稳定性明显更大(半衰期在 21-69 天之间)。EL 水的添加也能够抑制姜黄素及其衍生物的碱性水解,它们在水-EL30:70v/v 中的半衰期在 pH=8.6 时在 40-70h 之间。上述证据表明,EL 是从姜黄中提取姜黄素的一种很有前途的溶剂,也是将这些化合物输送到药物或食品中的合适介质。

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