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超高效超临界流体色谱法测定挪威云杉样品中的二萜树脂酸含量

Ultra High-Performance Supercritical Fluid Chromatography for the Quantitation of Diterpene Resin Acids in Norway Spruce Samples.

作者信息

Goels Thomas, Eichenauer Elisabeth, Langeder Julia, Aichner Georg F, Mauser Gregor, Amtmann Luisa, Grienke Ulrike, Glasl Sabine

机构信息

Division of Pharmacognosy, Department of Pharmaceutical Sciences, Faculty of Life Sciences, University of Vienna, Vienna, Austria.

Vienna Doctoral School of Pharmaceutical, Nutritional and Sport Sciences, University of Vienna, Vienna, Austria.

出版信息

Front Pharmacol. 2022 Jun 13;13:906411. doi: 10.3389/fphar.2022.906411. eCollection 2022.

DOI:10.3389/fphar.2022.906411
PMID:35770082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9234136/
Abstract

(L.) H. Karst. (Pinaceae) is native to Northern, Central and Eastern Europe. The fast-growing tree reaches up to 50 m in height, has modest nutritional requirements and depends on sufficient water supply. The conifer, commonly called Norway spruce, produces exudates which are traditionally used to treat skin wounds in Northern European countries. Major bioactive constituents of the conifer oleoresin are diterpene resin acids (DRAs) of the abietane and the pimarane type. To assure consistent pharmaceutical quality of Norway spruce balm and commercial products thereof, an analytical method for the quantitation of DRAs is the prerequisite. However, high structural similarity among DRAs and their poor UV absorption makes chromatographic separation and detection challenging: Conventional liquid chromatography systems often fail to achieve sufficient separation, moreover, they are not sustainable. Gas chromatography on the other hand requires time-consuming derivatization prior to unacceptably long analyses (>60 min). These drawbacks prompted the development of the first validated supercritical fluid-based protocol for the separation and quantitation of eight DRAs, i.e., pimaric acid (), sandaracopimaric acid (), palustric acid (), isopimaric acid (), levopimaric acid (), abietic acid (), dehydroabietic acid (), and neoabietic acid (). By using an ultra high-performance supercritical fluid chromatography (UHPSFC) device hyphenated to a quadrupole mass detector, the DRAs were separated in less than 20 min on a Torus 2-Picolylamin (2-PIC) column (3.0 mm × 100 mm; 1.7 µm particle size) applying supercritical CO and ethanol as mobile phase. Regarding selectivity, accuracy (recovery rates: 87-108%), intermediate precision (between 6.6 and 11.1%), and linearity (R ≥ 0.99; linear between 0.75 μg/ml and 2.5 mg/ml), results were obtained in line with ICH guidelines. The lowest limit of detection (LOD) was at 0.75 μg/ml () and the lowest limit of quantitation (LOQ) at 2 μg/ml (). As application examples, 22 Norway spruce balm samples and five commercial products were analyzed. The here presented protocol not only simplifies and shortens the analytical workflow, but also reduces the amount of organic solvent waste by about two thirds compared to conventional liquid chromatographic set-ups. These advantages qualify this fast and efficient method as an ideal tool for an environmentally friendly quality control of traditionally used wound-healing Norway spruce balm products.

摘要

欧洲云杉(L.)H. Karst.(松科)原产于北欧、中欧和东欧。这种生长迅速的树可高达50米,营养需求适中,依赖充足的水源供应。这种针叶树,通常被称为挪威云杉,会产生渗出物,在北欧国家传统上用于治疗皮肤伤口。针叶树油性树脂的主要生物活性成分是枞酸型和海松酸型的二萜树脂酸(DRAs)。为确保挪威云杉香脂及其商业产品具有一致的药品质量,定量分析DRAs的方法是先决条件。然而,DRAs之间高度的结构相似性以及它们较差的紫外吸收使得色谱分离和检测具有挑战性:传统液相色谱系统常常无法实现充分分离,而且它们不具有可持续性。另一方面,气相色谱在进行长得难以接受的分析(>60分钟)之前需要耗时的衍生化过程。这些缺点促使人们开发了首个经过验证的基于超临界流体的方法,用于分离和定量8种DRAs,即海松酸、山达海松酸、湿地松酸、异海松酸、左旋海松酸、枞酸、去氢枞酸和新枞酸。通过使用与四极杆质量检测器联用的超高效超临界流体色谱(UHPSFC)设备,在Torus 2 - 吡啶甲基胺(2 - PIC)柱(3.0毫米×100毫米;粒径1.7微米)上,以超临界CO₂和乙醇作为流动相,在不到20分钟的时间内分离了DRAs。在选择性、准确度(回收率:87 - 108%)、中间精密度(6.6%至11.1%之间)和线性度(R²≥0.99;在0.75微克/毫升至2.5毫克/毫升之间呈线性)方面,获得的结果符合国际协调会议(ICH)指南。最低检测限(LOD)为0.75微克/毫升(),最低定量限(LOQ)为2微克/毫升()。作为应用实例,分析了22个挪威云杉香脂样品和5种商业产品。此处介绍的方法不仅简化和缩短了分析流程,而且与传统液相色谱装置相比,有机溶剂废物量减少了约三分之二。这些优点使这种快速高效的方法成为对传统使用的伤口愈合挪威云杉香脂产品进行环境友好型质量控制的理想工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/793dddc63257/fphar-13-906411-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/54b6e5eb12fb/fphar-13-906411-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/3a9dab65d7c6/fphar-13-906411-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/793dddc63257/fphar-13-906411-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/54b6e5eb12fb/fphar-13-906411-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/3a9dab65d7c6/fphar-13-906411-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a1c/9234136/793dddc63257/fphar-13-906411-g003.jpg

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