Nakhonchai Nongnapas, Prompila Nattaya, Ponhong Kraingkrai, Siriangkhawut Watsaka, Vichapong Jitlada, Supharoek Sam-Ang
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, Thailand.
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, Thailand; Multidisciplinary Research Unit of Pure and Applied Chemistry, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, Thailand.
Talanta. 2024 May 1;271:125645. doi: 10.1016/j.talanta.2024.125645. Epub 2024 Jan 8.
Unmodified hairy basil seed mucilage (Ocimum basilicum L.), with attractive features as structural functionality and adsorption capacity, was employed as a green biosorbent for dispersive solid phase extraction and enrichment of oxytetracycline, tetracycline, and doxycycline before quantitation by HPLC-UV for the first time. Hairy basil crushed seed increased the contacting surface area and was completely dispersed in the sample solution to extract tetracyclines under acidic condition with the assistance of ultrasonic waves. The analytes in the extraction phase were separated on a C column under isocratic condition with a mobile phase consisted of acetonitrile and trifluoroacetic acid. Influence of chemical and physical variables on the extraction efficiency of the developed method was investigated and optimized systematically. Under the optimal condition of all experimental parameters, good linear ranges were obtained at 15.0-500 μg L for tetracyclines with determination coefficients more than 0.9994. Limits of detection (LODs) and limits of quantitation (LOQs) ranged 5.0-7.0 and 15.0 μg L, respectively. Relative standard deviations (RSDs) of the proposed method at 100 and 300 μg L for TCs were less than 13 % and 10 %, respectively with percentage TC recoveries from spiked standard ranging 83.1-109.9 %. This simple, reliable, cost-effective, and environmentally friendly method was successfully applied for the analysis of tetracycline residues in milk. The greenness of the proposed method was assessed using the Analytical Eco-Scale and AGREE protocol.
未改性的毛罗勒种子黏液(罗勒)具有结构功能性和吸附能力等吸引人的特性,首次被用作绿色生物吸附剂,用于在通过高效液相色谱-紫外检测法定量之前,对土霉素、四环素和强力霉素进行分散固相萃取和富集。毛罗勒碾碎的种子增加了接触表面积,并在超声波辅助下在酸性条件下完全分散在样品溶液中以萃取四环素。萃取相中的分析物在等度条件下于C柱上分离,流动相由乙腈和三氟乙酸组成。系统地研究并优化了化学和物理变量对所开发方法萃取效率的影响。在所有实验参数的最佳条件下,四环素在15.0 - 500 μg/L范围内获得了良好的线性范围,测定系数大于0.9994。检测限(LOD)和定量限(LOQ)分别为5.0 - 7.0 μg/L和15.0 μg/L。所提出方法在100和300 μg/L的四环素浓度下的相对标准偏差(RSD)分别小于13%和10%,加标标准品中四环素的回收率为83.1 - 109.9%。这种简单、可靠、经济高效且环保的方法成功应用于牛奶中四环素残留的分析。使用分析生态量表和AGREE协议评估了所提出方法的绿色度。