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超声辅助提取-气相色谱-质谱法测定外用制剂中大麻二酚的含量

An improved method for the determination of cannabidiol in topical products using ultrasound-assisted extraction and gas chromatography-mass spectrometry.

机构信息

Department of Physical Sciences (Chemistry), Faculty of Science, Thompson Rivers University, 805 TRU Way, Kamloops, BC, Canada.

Department of Biological Sciences, Faculty of Science, Thompson Rivers University, 805 TRU Way, Kamloops, BC, Canada.

出版信息

J Pharm Biomed Anal. 2022 Aug 5;217:114840. doi: 10.1016/j.jpba.2022.114840. Epub 2022 May 20.

Abstract

The recent surge in the sale of cannabidiol (CBD)-based topicals has risen rapidly in recent years, as it can be used to treat a multitude of skin disorders. However, there is minimal regulation concerning actual CBD content in these products. Topicals on the market may contain various concentrations of CBD and may be combined with a range of other compounds. The concentration of CBD has to be determined before the products enter the market. For this reason, a selective analytical method was developed using a 2 factorial design; and validated to determine CBD content in various topicals based on ultrasound-assisted extraction (UAE) followed by gas chromatography coupled to mass spectrometry (GC-MS). The method showed good precision (relative standard deviation ≤ 7.7%), accuracy at three concentration levels (recovery > 97.9%) for three different matrices, acceptable linearity (R > 0.99), and limit of detection (0.05 µg/mg). The method was successfully applied to the analysis of five commercial topicals. The proposed method is rapid, sensitive, precise, and accurate. In addition, it does not require derivatization and it is suitable for the determination of CBD in topicals for quality control purposes.

摘要

近年来,含有大麻二酚 (CBD) 的局部用药的销售额迅速增长,因为它可用于治疗多种皮肤疾病。然而,这些产品中 CBD 的实际含量几乎没有受到监管。市面上的外用制剂可能含有不同浓度的 CBD,并且可能与多种其他化合物结合使用。在产品进入市场之前,必须确定 CBD 的浓度。出于这个原因,采用 2 因子设计建立了一种选择性分析方法;并进行了验证,以使用基于超声辅助提取 (UAE) 随后结合气相色谱-质谱联用 (GC-MS) 的方法来确定各种局部制剂中的 CBD 含量。该方法在三个不同基质中,在三个浓度水平下表现出良好的精密度(相对标准偏差≤7.7%)、准确度(回收率>97.9%)、可接受的线性度(R>0.99)和检测限(0.05μg/mg)。该方法成功应用于五种商业局部制剂的分析。该方法快速、灵敏、精确、准确。此外,它不需要衍生化,适用于局部制剂中 CBD 的定量控制目的。

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