Forensic Toxicology Division, Central Forensic Science Laboratory, Urput-Kumeria Road, P.O. Maniari Tiniali, Kamrup (Rural), Assam 781125, India.
Forensic Toxicology Division, Central Forensic Science Laboratory, Plot #2, Sector 36-A, Dakshin Marg, Chandigarh 160036, India, and.
J Chromatogr Sci. 2020 Apr 25;58(5):477-484. doi: 10.1093/chromsci/bmaa007.
A simple, rapid, cost-effective and green analytical method is developed based on ultrasound-assisted dispersive liquid-liquid microextraction (US-DLLME) coupled to thin-layer chromatography (TLC)-image analysis for the simultaneous determination of two major alkaloids of Strychnos nux-vomica L i.e., strychnine and brucine. The method is composed of three steps, namely (i) US-DLLME by injecting a mixture of 100-μL chloroform (extraction solvent) and 1-mL methanol (disperser solvent) in 5 mL of aqueous sample, followed by ultrasonication and centrifugation, (ii) TLC of 20 μL of sedimented phase with methanol: ammonia (100:1.5, v/v) as the mobile phase and visualization under ultraviolet radiation (254 nm) and (iii) photography of TLC plate and quantification of spots by image analysis using freely available imageJ software (National Institute of Health, Bethesda, MD, USA). The limit of detection and limit of quantification for both alkaloids were found to be in the range of 0.12-0.15 and 0.36-0.48 μg/spot, respectively. The method was found to be linear in the range of 0.5-5 μg/spot with correlation coefficient (R2) of 0.995 and 0.997 for strychnine and brucine, respectively. The developed method was successfully applied for the determination of strychnine and brucine in Ayurvedic formulations and blood samples. The method does not require any sophisticated instrument and handling skills and can be adopted for rapid analysis of strychnine and brucine in forensic toxicological laboratories.
建立了一种基于超声辅助分散液液微萃取(US-DLLME)与薄层色谱(TLC)-图像分析联用的简单、快速、经济、绿色的分析方法,用于同时测定马钱子中两种主要生物碱即士的宁和马钱子碱的含量。该方法由三个步骤组成:(i)在 5 mL 水样品中注入 100 μL 氯仿(萃取溶剂)和 1 mL 甲醇(分散溶剂)的混合物,然后进行超声处理和离心,(ii)用甲醇:氨水(100:1.5,v/v)作为流动相对 20 μL 沉淀相进行 TLC,并在紫外辐射(254nm)下进行可视化,(iii)对 TLC 板进行拍照并用免费的图像分析软件(美国马里兰州贝塞斯达国立卫生研究院)对斑点进行定量分析。两种生物碱的检测限和定量限分别为 0.12-0.15 和 0.36-0.48 μg/点。该方法在线性范围内为 0.5-5 μg/点,士的宁和马钱子碱的相关系数(R2)分别为 0.995 和 0.997。该方法成功应用于阿育吠陀配方和血液样本中士的宁和马钱子碱的测定。该方法不需要任何复杂的仪器和操作技能,可用于法医毒理学实验室中士的宁和马钱子碱的快速分析。