Department of Chemistry, Faculty of Science, Lorestan University, Khoramabad, Iran.
Talanta. 2010 Mar 15;80(5):1926-31. doi: 10.1016/j.talanta.2009.10.051. Epub 2009 Oct 31.
A reversed-phase dispersive liquid-liquid microextraction (RP-DLLME) method was developed for the preconcentration and direct HPLC determination of oleuropein in olive's processing wastewater (OPW) and olive leaves extracts. In conventional DLLME, the sedimented phase is a micro-drop of a chlorinated organic solvent that is not compatible with RP-HPLC. Therefore, solvent evaporation and reconstitution with an appropriate solvent is often required. In RP-DLLME, this problem was overcome by overturning the solvent polarity in the ordinary DLLME and replacing the organic solvent with water. A central composite chemometrics design was used for multivariate optimization of the effects of five different parameters influencing the extraction efficiency of the method. In the optimized conditions, a mixture of 1.4 mL of an ethyl acetate extract of sample and 40 microL water (pH 5.0) was rapidly injected into 5.3 mL of cyclohexane. After centrifugation of the formed cloudy mixture, a micro-drop of the aqueous phase was sedimented at the conical bottom of the centrifuge tube. This phase, that contained the preconcentrated and partially purified analyte, was directly injected into an RP-HPLC column for analysis. A mean extraction recovery of 102.5 (+/-4.5) % with enrichment factors exceeding 38, was obtained for five replicated analysis. The detection limit of the method (3 sigma) for OE was 0.02 microg L(-1) for OPW and 2 x 10(-3) mg kg(-1) for olive leaves samples. The results showed that, RP-DLLME is a promising technique which is quick, easily operated and can be directly coupled to HPLC.
反相分散液液微萃取(RP-DLLME)法用于橄榄加工废水中(OPW)和橄榄叶提取物中橄榄苦苷的预浓缩和直接 HPLC 测定。在常规 DLLME 中,沉淀相是不与 RP-HPLC 兼容的氯化有机溶剂的微滴。因此,通常需要蒸发溶剂并用适当的溶剂重新配制。在 RP-DLLME 中,通过颠倒普通 DLLME 中的溶剂极性并用水代替有机溶剂来解决此问题。使用中心组合化学计量学设计对影响方法萃取效率的五个不同参数的影响进行了多元优化。在优化条件下,将 1.4 mL 样品的乙酸乙酯萃取物和 40 μL 水(pH 5.0)快速注入 5.3 mL 环己烷中。形成的混浊混合物离心后,在离心管的锥形底部沉淀下水相的微滴。该相包含预浓缩和部分纯化的分析物,直接注入 RP-HPLC 柱进行分析。五次重复分析的平均萃取回收率为 102.5(+/-4.5)%,富集因子超过 38。该方法(3sigma)对 OE 的检测限为 OPW 中的 0.02 微克 L(-1)和橄榄叶样品中的 2 x 10(-3)mg kg(-1)。结果表明,RP-DLLME 是一种快速、易于操作且可直接与 HPLC 耦合的有前途的技术。