Development and validation of an HPLC-DAD method for the quantification of cannabigerol, cannabidiol, cannabinol and cannabichromene in human plasma and mouse matrices†

IF 3.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL Analyst Pub Date : 2024-06-07 DOI:10.1039/D4AN00070F
Andreia Carona, Joana Bicker, Carla Fonseca, Maria da Graça Campos, Amílcar Falcão and Ana Fortuna
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Abstract

Cannabigerol, cannabidiol, cannabinol and cannabichromene are non-psychoactive phytocannabinoids, highly present in Cannabis sativa, for which numerous therapeutical applications have been described. However, additional pre-clinical and clinical data, including toxicopharmacokinetic and pharmacodynamic studies, remain required to support their use in clinical practice and new therapeutic applications. To support these studies, a new high performance liquid chromatography technique (HPLC) with diode-array detection (DAD) was developed and validated to quantify these cannabinoids in human plasma and mouse matrices. Sample extraction was accomplished by protein precipitation and double liquid–liquid extraction. Simvastatin and perampanel were used as internal standards in human and mouse matrices, respectively. Chromatographic separation was achieved in 16 min on an InfinityLab Poroshell® 120 C18 column (4.6 mm × 100 mm, 2.7 μm) at 40 °C. A mobile phase composed of water/acetonitrile was pumped with a gradient elution program at 1.0 mL min−1. The technique revealed linearity in the defined concentration ranges with a determination coefficient of over 0.99. Intra and inter-day accuracy and precision values ranged from −14.83 to 13.97% and 1.08 to 13.74%, respectively. Sample stability was assessed to ensure that handling and storage conditions did not compromise analyte concentrations in different matrices. Carry-over was absent and recoveries were over 77.31%. This technique was successfully applied for the therapeutic monitoring of cannabidiol and preliminary pre-clinical studies with cannabigerol and cannabidiol. All samples were within calibration ranges, with the exception of cannabigerol after intraperitoneal administration. This is the first HPLC-DAD technique that simultaneously quantifies cannabinoids in these biological matrices, supporting future pre-clinical and clinical investigations.

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开发并验证 HPLC-DAD 方法,用于定量检测人血浆和小鼠基质中的大麻酚、大麻二酚、大麻酚和大麻色烯。
大麻酚、大麻二酚、大麻酚和大麻色烯是非精神活性植物大麻素,在大麻中含量很高,已有大量治疗应用的描述。不过,仍需要更多的临床前和临床数据,包括毒物药代动力学和药效学研究,以支持它们在临床实践中的使用和新的治疗应用。为了支持这些研究,我们开发并验证了一种新型高效液相色谱技术(HPLC)和二极管阵列检测技术(DAD),用于定量检测人体血浆和小鼠基质中的这些大麻素。样品提取采用蛋白沉淀和双液液相萃取法。辛伐他汀和帕潘奈尔分别用作人和小鼠基质中的内标。采用InfinityLab Poroshell® 120 C18色谱柱(4.6 mm × 100 mm, 2.7 μm),在40 °C条件下,16分钟内完成色谱分离。流动相为水/乙腈,梯度洗脱速度为 1.0 mL/min-1。该技术在规定的浓度范围内呈线性关系,测定系数超过 0.99。日内和日间的准确度和精密度分别为-14.83%至13.97%和1.08%至13.74%。对样品的稳定性进行了评估,以确保处理和储存条件不会影响不同基质中分析物的浓度。结果表明,样品中不存在残留物,回收率超过 77.31%。该技术已成功应用于大麻二酚的治疗监测以及大麻萜醇和大麻二酚的初步临床前研究。除腹腔给药后的大麻酚外,所有样品均在校准范围内。这是首个能同时对这些生物基质中的大麻素进行定量的 HPLC-DAD 技术,为未来的临床前和临床研究提供了支持。
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来源期刊
Analyst
Analyst 化学-分析化学
CiteScore
7.80
自引率
4.80%
发文量
636
审稿时长
1.9 months
期刊介绍: The home of premier fundamental discoveries, inventions and applications in the analytical and bioanalytical sciences
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