Citrus×limon (L) Osbeck 叶精油的化学成分分析及其作为抗宫颈癌剂的活性

Iffat Syafiqoh Afif, S. Suryati, A. Santoni
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摘要

宫颈癌是一种危及生命的疾病。使用合成药物治疗会对身体产生严重的不良影响。因此,有必要寻找对人体安全的天然药物。植物中含有的次级代谢产物之一是精油,众所周知,精油具有抗宫颈癌的活性。柑橘属因含有 EO 化合物而闻名,该属的一个物种是 Citrus×lemon (L) Osbeck。本研究的目的是鉴定从柑橘叶中分离出来的环氧乙烷的化学成分,并评估其对宫颈癌的细胞毒活性。研究人员采用水蒸馏法从印度尼西亚巴东市采集的 C×limon 树叶中分离出环氧乙烷。然后用 GC-MS 对环氧乙烷进行分析。为确定其细胞毒性,进行了 BSLT 试验,然后进行了分子对接和 MTT 试验。实验得到了一种黄色液体,密度为 0.8684 克/毫升,产率为 0.181%。环氧乙烷的气相色谱-质谱分析鉴定出了 56 种化学成分,主要化合物为(-)-β-蒎烯(7.32%)、(-)-柠檬烯(28.40%)、香叶醇(5.54%)、石竹烯(5.22%)。环氧乙烷对盐蒿幼虫的毒性很高,半数致死浓度为 3,697 微克/毫升。通过分子对接,已知环氧乙烷中的主要化合物(-)-柠檬烯、香叶醇、(-)β-蒎烯和叶绿素化合物能与宫颈癌蛋白(HPV18E6)结合形成复合物。MTT 检测显示,环氧乙烷对 HeLa 细胞的细胞毒性较弱,IC50 为 218.9 µg/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemical Composition Analysis of Citrus×limon (L) Osbeck Leaf Essential Oil and Its Activity as an Anti-Cervical Cancer Agent
Cervical cancer is a life-threatening disease. The use of synthetic drugs for its treatment can have serious adverse effects on the body. Therefore, it is necessary to search for natural drugs that are safe for the body. One of the secondary metabolites contained in plants is essential oils (EO), EO are known to have activity as anti-cervical cancer. Genus Citrus is known for containing EO compounds, one of the species of the genus is Citrus×lemon (L) Osbeck. The purpose of this study is to identify the chemical components of the EO isolated from the leaves of C×limon and to evaluate its cytotoxic activity against cervical cancer. EO was isolated from C×limon leaves collected in Padang City, Indonesia using the hydrodistillation method. EO was then analyzed by GC-MS. To determine its cytotoxicity, BSLT was conducted, followed by molecular docking and MTT assays. The experiment yielded a yellow liquid with a density of 0,8684 g/mL and a yield of 0,181%. GC-MS analysis of the EO identified 56 chemical components, with the main compounds are (-)-β-pinene (7.32%), (-)-limonene (28.40%), geranial (5.54%), caryophyllene (5.22%). The EO showed high toxicity against Artemia salina L larvae, with an LC50 value of 3,697 µg/mL. Through molecular docking, it is known the (-)-limonene, geranial, (-)β-pinene and caryophyllene compounds as the main compounds in of EO are known to bind to form complexes with cervical cancer proteins (HPV18E6). MTT assay showed weak cytotoxic activity of EO against HeLa cells, with an IC50 of 218.9 µg/mL.
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