Determination and Confirmation of Psychedelic and Psychoactive Compounds in Botanical Materials by UPLC-ESI-MS/MS: Single Laboratory Validation.

IF 1.7
Torey French, Anthony J Fontana, Robert LaBudde, Sharon L Brunelle, Sidney Sudberg
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Abstract

Background: A multi-analyte method was developed for determination and confirmation of 26 natural and synthetic psychedelic and psychoactive compounds from botanical sources using a simple extraction procedure and UPLC-ESI-MS/MS analysis.

Objective: The objective of this work was to develop and validate the method for analysis of psychedelic and psychoactive compounds in botanicals (fungi, cactus, leaf), extract (brewed tea), synthetic and simulated finished product (using maltodextrin).

Methods: The method uses an acidified methanol solution for extraction and diphenhydramine as internal standard. Extracts are subjected to UPLC with tandem mass spectrometry using a phenyl-hexyl column and acidified mobile phase with acetonitrile gradient. Validation studies followed US Pharmacopeia <1225> and Official Methods of Analysis  SM Appendix K guidelines to assess specificity, accuracy (recovery), repeatability and intermediate precision, limits of detection and quantification, calibration curve linearity, system suitability, and robustness.

Results: Average recovery of spiked replicates in matrix and surrogate matrixes varied between 88-124% for analytes in fungi, cactus, and leaf matrixes; 81-106% in brewed tea matrix; and 81-174% across all 26 analytes in maltodextrin. Norbaeocystin and harmaline were the only analytes outside the acceptance criterion (79-126%) in maltodextrin. The 90% upper confidence limit on repeatability was ≤33% for all analytes and matrixes except for norbaeocystin. Repeatability precision for analysis of matrixes with native analytes met the acceptance criterion of ≤ 33% in all cases and the 90% upper confidence limit on intermediate precision was ≤35% in all cases. LOQ values fell below the lowest calibration standard (0.016 µg/mL) for all 26 analytes.

Conclusion: The method met the pre-determined acceptance criteria for recovery and precision in nearly all cases. Calibration curve linearity and system suitability measures were established.

Highlights: A method for 26 psychedelic/psychoactive compounds was validated for analysis of botanical (fungi, cactus, leaf), extract (brewed tea), synthetic and simulated finished product (using maltodextrin) using native and surrogate botanicals.

UPLC-ESI-MS/MS法测定植物材料中致幻剂和精神活性物质:单实验室验证
背景:建立了一种多分析方法,通过简单的提取程序和UPLC-ESI-MS/MS分析,对植物源中26种天然和合成的致幻剂和精神活性化合物进行测定和确认。目的:建立和验证植物(真菌、仙人掌、叶子)、提取物(泡茶)、合成和模拟成品(使用麦芽糖糊精)中致幻剂和精神活性物质的分析方法。方法:采用酸化甲醇溶液萃取,以苯海拉明为内标。萃取物采用苯己基柱和乙腈梯度酸化流动相进行UPLC串联质谱分析。验证研究遵循美国药典和官方分析方法SM附录K指南,评估特异性、准确度(回收率)、可重复性和中间精密度、检测和定量限、校准曲线线性、系统适用性和鲁棒性。结果:在真菌、仙人掌和叶子基质中,加标重复物在基质和替代基质中的平均回收率在88-124%之间;冲泡茶基质中含量为81-106%;在所有26种分析物中,麦芽糊精含量为81-174%。麦芽糖糊精中只有去甲半胱氨酸和海蜂碱超出可接受标准(79-126%)。除去甲毛囊素外,所有分析物和基质的重复性90%置信上限≤33%。用原生分析物分析基质的重复性精密度均满足≤33%的可接受标准,中间精密度的90%置信上限均≤35%。所有26种分析物的LOQ值均低于最低校准标准(0.016µg/mL)。结论:该方法在回收率和精密度方面基本满足预定的验收标准。建立了标定曲线线性度和系统适宜性指标。重点:验证了26种迷幻/精神活性化合物的方法,用于分析植物(真菌,仙人掌,叶子),提取物(冲泡茶),合成和模拟成品(使用麦芽糊精),使用天然和替代植物药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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