crinine and lycorine

An undisputed trend in sample preparation at present is to meet the requirements of green chemistry especially in the field of natural products. Green technology continuously pursues new solvents to replace common organic solvents that possess inherent toxicity. Over the past two decades, non-ionic surfactants have gained enormous attention from the scientific community. The micelle-mediated extraction and cloud-point preconcentration (CPE) methods offer a convenient alternative to the conventional extraction systems. Recently, natural deep eutectic solvents (NDESs) have emerged as green and sustainable solvents for efficient extraction of bioactive compounds or drugs. They are generally composed of neutral, acidic or basic compounds that form liquids of high viscosity when mixed in certain molar ratio. The presented work aimed to comprehensively compare and evaluate the potential and effectiveness of NDES as well as non-ionic surfactants (Genapol X-080, Triton X-100 and Triton X-114) for extraction of Amaryllidaceae alkaloids from Crinum powellii bulbs as representative example of plant material, in comparison to the conventional solvents (methanol, ethanol and water).A new validated high-performance thin-layer chromatographic (HPTLC) method has been developed for the simultaneous quantitation of three alkaloids markers, lycorine, crinine and crinamine, in the bulbs of C. powellii. Extraction efficiency of the targeted alkaloids from the bulb matrix with organic and ecofriendly (green) solvents were studied. Results revealed that NDES and surfactants were significantly more efficient in alkaloid extraction than previous methods requiring the consumption of organic solvents and water. Genapol X-80 demonstrated 138%, 149% and 145%, while choline chloride: fructose (5:2): H

Topics: Alkaloids; Amaryllidaceae Alkaloids; Biological Products; Chromatography, Thin Layer; Crinum; Green Chemistry Technology; Phenanthridines; Plant Extracts; Solvents; Surface-Active Agents; Water

To study the chemical constituents of the Bulbs of Lycoris longituba.. The chemical constituents were isolated and purified by means of chromatographic techniques and their structures were elucidated by spectroscopic methods.. Six compounds were isolated and identified as Crinine (1), Narciclasine (2), Squamigine (3), 11-Hydroxyvittatine (4), Pancracine (5), Lycorine (6).. Compounds 1 - 6 are isolated from this plant for the first time.

Topics: Amaryllidaceae Alkaloids; China; Heterocyclic Compounds, 4 or More Rings; Lycoris; Magnetic Resonance Spectroscopy; Molecular Structure; Phenanthridines; Plant Roots