{"title":"Development of a novel isolation method for Δ<sup>9</sup>-tetrahydrocannabinolic acid-A from cannabis suitable for forensic laboratories.","authors":"Kenji Tsujikawa, Yuki Okada, Tadashi Yamamuro, Kenji Kuwayama, Tatsuyuki Kanamori, Yuko T Iwata","doi":"10.1007/s11419-025-00742-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Δ<sup>9</sup>-Tetrahydrocannabinolic acid-A (Δ<sup>9</sup>-THCA-A) is a precursor of Δ<sup>9</sup>-tetrahydrocannabinol in cannabis. Here, considering applicability to ordinary forensic laboratories, we developed a novel isolation method for Δ<sup>9</sup>-THCA-A without the need for special equipment.</p><p><strong>Methods: </strong>Dried pulverized cannabis inflorescence (2 g) was extracted with acetonitrile. After the extract was treated with graphite carbon powder to remove chlorophyll, the solvent was replaced with methanol. The methanol solution was diluted with aqueous sodium hydroxide solution and then washed with a mixture of n-hexane/ethyl acetate (7:1, v/v). The remaining aqueous layer was acidified with acetic acid and extracted with the n-hexane/ethyl acetate mixture. The extract was purified by silver nitrate-impregnated silica gel column chromatography.</p><p><strong>Results: </strong>The isolation procedure gave a pale beige solid as the final product. The final product was identified as Δ<sup>9</sup>-THCA-A by comparison of the analytical results of gas chromatography/mass spectrometry (GC/MS) after trimethylsilylation and high-performance liquid chromatography with ultraviolet detection (HPLC-UV) with an authentic standard. The final product was confirmed to be highly pure by <sup>1</sup>H-nuclear magnetic resonance spectroscopy in addition to GC/MS and HPLC-UV.</p><p><strong>Conclusions: </strong>This novel isolation method gave highly pure Δ<sup>9</sup>-THCA-A without using special purification equipment, such as a flash chromatography system or an HPLC system with a fraction collector, which are uncommon in forensic laboratories. This method will be useful for many forensic laboratories that find it difficult to obtain commercial Δ<sup>9</sup>-THCA-A as a standard.</p>","PeriodicalId":12329,"journal":{"name":"Forensic Toxicology","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Forensic Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11419-025-00742-3","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Δ9-Tetrahydrocannabinolic acid-A (Δ9-THCA-A) is a precursor of Δ9-tetrahydrocannabinol in cannabis. Here, considering applicability to ordinary forensic laboratories, we developed a novel isolation method for Δ9-THCA-A without the need for special equipment.
Methods: Dried pulverized cannabis inflorescence (2 g) was extracted with acetonitrile. After the extract was treated with graphite carbon powder to remove chlorophyll, the solvent was replaced with methanol. The methanol solution was diluted with aqueous sodium hydroxide solution and then washed with a mixture of n-hexane/ethyl acetate (7:1, v/v). The remaining aqueous layer was acidified with acetic acid and extracted with the n-hexane/ethyl acetate mixture. The extract was purified by silver nitrate-impregnated silica gel column chromatography.
Results: The isolation procedure gave a pale beige solid as the final product. The final product was identified as Δ9-THCA-A by comparison of the analytical results of gas chromatography/mass spectrometry (GC/MS) after trimethylsilylation and high-performance liquid chromatography with ultraviolet detection (HPLC-UV) with an authentic standard. The final product was confirmed to be highly pure by 1H-nuclear magnetic resonance spectroscopy in addition to GC/MS and HPLC-UV.
Conclusions: This novel isolation method gave highly pure Δ9-THCA-A without using special purification equipment, such as a flash chromatography system or an HPLC system with a fraction collector, which are uncommon in forensic laboratories. This method will be useful for many forensic laboratories that find it difficult to obtain commercial Δ9-THCA-A as a standard.
用途:Δ9-Tetrahydrocannabinolic酸- a (Δ9-THCA-A)是大麻中Δ9-tetrahydrocannabinol的前体。在这里,考虑到适用于普通法医实验室,我们开发了一种新的隔离方法Δ9-THCA-A不需要特殊设备。方法:用乙腈提取干大麻花粉(2g)。提取液经石墨碳粉处理去除叶绿素后,用甲醇代替溶剂。甲醇溶液用氢氧化钠水溶液稀释,然后用正己烷/乙酸乙酯(7:1,v/v)的混合物洗涤。剩余水层用乙酸酸化,用正己烷/乙酸乙酯混合物萃取。提取液采用硝酸银-硅胶柱层析纯化。结果:分离得到的最终产物为淡米色固体。将三甲基硅基化后的气相色谱/质谱(GC/MS)分析结果与具有正品标准的高效液相色谱-紫外检测(HPLC-UV)分析结果进行比较,确定最终产品为Δ9-THCA-A。经1h -核磁共振波谱、GC/MS、HPLC-UV等方法验证,最终产物纯度高。结论:该分离方法不需要特殊的纯化设备,如闪蒸层析系统或带组分收集器的高效液相色谱系统,可获得高纯度的Δ9-THCA-A,这在法医实验室中并不常见。这种方法将对许多难以获得商业Δ9-THCA-A作为标准的法医实验室有用。
期刊介绍:
The journal Forensic Toxicology provides an international forum for publication of studies on toxic substances, drugs of abuse, doping agents, chemical warfare agents, and their metabolisms and analyses, which are related to laws and ethics. It includes original articles, reviews, mini-reviews, short communications, and case reports. Although a major focus of the journal is on the development or improvement of analytical methods for the above-mentioned chemicals in human matrices, appropriate studies with animal experiments are also published.
Forensic Toxicology is the official publication of the Japanese Association of Forensic Toxicology (JAFT) and is the continuation of the Japanese Journal of Forensic Toxicology (ISSN 0915-9606).