Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11221 Belgrade, Serbia.
Innovation Center of the Faculty of Technology and Metallurgy, Karnegijeva 4, 11120 Belgrade, Serbia.
Molecules. 2023 Mar 5;28(5):2395. doi: 10.3390/molecules28052395.
A fast and straightforward reversed-phase dispersive liquid-liquid microextraction (RP-DLLME) using a deep eutectic solvent (DES) procedure to determine free tryptophan in vegetable oils was developed. The influence of eight variables affecting the RP-DLLME efficiency has been studied by a multivariate approach. A Plackett-Burman design for screening the most influential variables followed by a central composite response surface methodology led to an optimum RP-DLLME setup for a 1 g oil sample: 9 mL hexane as the diluting solvent, vortex extraction with 0.45 mL of DES (choline chloride-urea) at 40 °C, without addition of salt, and centrifugation at 6000 rpm for 4.0 min. The reconstituted extract was directly injected into a high-performance liquid chromatography (HPLC) system working in the diode array mode. At the studied concentration levels, the obtained method detection limits (MDL) was 11 mg/kg, linearity in matrix-matched standards was R ≥ 0.997, relative standard deviations (RSD) was 7.8%, and average recovery was 93%. The combined use of the recently developed DES -based RP-DLLME and HPLC provides an innovative, efficient, cost-effective, and more sustainable method for the extraction and quantification of free tryptophan in oily food matrices. The method was employed to analyze cold-pressed oils from nine vegetables (Brazil nut, almond, cashew, hazelnut, peanut, pumpkin, sesame, sunflower, and walnut) for the first time. The results showed that free tryptophan was present in the range of 11-38 mg/100 g. This article is important for its contributions to the field of food analysis, and for its development of a new and efficient method for the determination of free tryptophan in complex matrices, which has the potential to be applied to other analytes and sample types.
一种使用深共晶溶剂(DES)程序快速直接的反相分散液相微萃取(RP-DLLME)方法被开发出来,用于测定植物油中的游离色氨酸。通过多元方法研究了影响 RP-DLLME 效率的八个变量。采用 Plackett-Burman 设计筛选最有影响的变量,然后采用中心复合响应面法,得到了适用于 1 g 油样的最佳 RP-DLLME 条件:9 mL 正己烷作为稀释溶剂,在 40°C 下用 0.45 mL 的 DES(氯化胆碱-尿素)涡旋萃取,无需加盐,6000 rpm 离心 4.0 min。重构后的萃取物直接注入高效液相色谱(HPLC)系统,工作在二极管阵列模式下。在所研究的浓度水平下,该方法的检测限(MDL)为 11 mg/kg,基质匹配标准的线性度 R≥0.997,相对标准偏差(RSD)为 7.8%,平均回收率为 93%。最近开发的基于 DES 的 RP-DLLME 和 HPLC 的联合使用为提取和定量油食品基质中的游离色氨酸提供了一种创新、高效、经济实惠且更可持续的方法。该方法首次用于分析来自九种蔬菜(巴西坚果、杏仁、腰果、榛子、花生、南瓜、芝麻、葵花籽和核桃)的冷榨油。结果表明,游离色氨酸的含量范围为 11-38 mg/100 g。本文对食品分析领域具有重要意义,它开发了一种新的、高效的方法,用于测定复杂基质中的游离色氨酸,该方法具有应用于其他分析物和样品类型的潜力。