加速溶剂萃取蓝睡莲产品中的阿波啡:植物材料绿色萃取的概念验证

Rohith Krishna, Anirudha Dixit, Ketan Patil, Shalvi Agrawal, Jilja Joseph, Astha Pandey, Mahipal Singh Sankhla
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摘要

蓝睡莲(睡莲)是一种美丽的水生植物,广泛分布在印度和非洲。蓝色睡莲含有一种叫做阿波啡的生物碱,据说是一种镇静剂,也是一种非选择性多巴胺激动剂,现在在当地和网上市场上以粉末和油的形式出售,用于各种用途,如帮助睡眠、缓解焦虑和增强性功能。这些特性被服用蓝花百合滥用,以达到一种“高”的状态,这导致了它被归类为一种新的精神活性物质。本文采用Waters Radian as soon - as - possible仪器对市售蓝睡莲产品进行快速质谱分析初步筛选,然后采用高效液相色谱-光电二极管阵列方法对样品进行开发和验证,用于阿波吗啡的定性和定量分析。加速溶剂萃取法是一种替代传统索氏萃取法的绿色萃取方法。最后利用复绿色分析程序指数法对该方法进行了绿色度筛选。方法线性度为0.9973;检测限为0.02µg/mL,定量限为0.18µg/mL。该方法能够对市售的两种海百合天然产物中的阿帕吗啡进行检测和定量。
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Accelerated solvent extraction of apomorphine from Nymphaea caerulea (Blue Water Lily) products: A proof-of-concept Green extraction for plant materials

Nymphaea caerulea (Blue water lily) is an esthetically pleasing aquatic plant which is widely located across India and Africa. The blue water lily contains an alkaloid called apomorphine which is said to be a sedative, and a nonselective dopamine agonist and is now available in the local and online market in the form of powders and oils for various applications such as sleeping aid, anxiety reliever and sexual performance enhancer. These properties are abused by the consumption of Nymphaea caerulea to achieve a state of “high” which has led the categorization of the same as a novel psychoactive substance. In this paper, a rapid mass spectral analysis was performed for the preliminary screening of commercially available blue water lily products using the Waters Radian as soon as possible instrument, followed by the high performance liquid chromatography-photo diode array method development and validation of the samples for the qualitative and quantitative analysis of apomorphine. Accelerated solvent extraction as a green alternative to the conventional soxhlet extraction was used in the extraction of the plant material. The method was finally screened for its greenness using the Complex green analytical procedure index method. The method was validated with a linearity of 0.9973; limit of detection and limit of quantitation of 0.02 and 0.18 µg/mL, respectively. The method was able to detect and quantitate apomorphine in two samples from the commercially available natural products of Nymphaea caerulea.

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