拉帕酮与同系物恩贝林的提取条件优化及细胞毒性比较
Optimization of Extraction Conditions and Cytotoxic Activity of Rapanone in Comparison to Its Homologue, Embelin.
机构信息
Department of Pharmacognosy, Pharmaceutical Faculty, Medical College, Jagiellonian University, Medyczna 9, 30-688 Cracow, Poland.
Department of Food Chemistry and Nutrition, Pharmaceutical Faculty, Medical College, Jagiellonian University, Medyczna 9, 30-688 Cracow, Poland.
出版信息
Molecules. 2022 Nov 16;27(22):7912. doi: 10.3390/molecules27227912.
Rapanone is a plant-derived simple alkyl-dihydroxybenzoquinone structurally close to embelin, a well-known cytotoxic agent. The pharmacological characterization of rapanone is still incomplete, and to fill the data gap, a good source for its acquisition is required to conduct further research. This study aimed to optimize the conditions for the extraction of rapanone from the leaves of white-berried Sims. For this purpose, three methods were employed: heat reflux (HRE), shaking (SE), and ultrasound-assisted extraction (UAE), and such parameters as the extraction time, solvent, and the number of extractions from the same sample were set as experimental variables. Furthermore, cytotoxic activity toward prostate cancer, thyroid cancer, and colorectal carcinoma cell lines was investigated and compared with doxorubicin and embelin. The most effective and economical method for the extraction of rapanone was shown to be 20 min UAE with ethyl acetate or chloroform. Rapanone exhibited high cytotoxic activity against PC3 (IC = 6.50 μg/mL), Du145 (IC = 7.68 μg/mL), FTC133 (IC = 6.01 μg/mL), 8505C (IC = 7.84 μg/mL), and Caco-2 (IC = 8.79 μg/mL) cell lines after 24 h and against the HT29 cell line after 48 h (IC = 11.67 μg/mL). Furthermore, it revealed a more favorable safety profile than either its homologue, embelin, or doxorubicin. The set of optimal extraction parameters obtained may be utilized for scientific and industrial purposes to achieve the best rapanone yield. Moreover, this benzoquinone revealed a high cytotoxic activity with good selectivity.
拉帕酮是一种植物来源的简单烷基二羟基苯醌,结构上与埃博霉素接近,埃博霉素是一种众所周知的细胞毒性剂。拉帕酮的药理学特征尚不完全,为了填补数据空白,需要有一个良好的来源来获取它,以便进行进一步的研究。本研究旨在优化从白浆果 Sims 叶中提取拉帕酮的条件。为此,采用了三种方法:热回流(HRE)、振荡(SE)和超声辅助提取(UAE),并将提取时间、溶剂和从同一样品中进行的提取次数等参数作为实验变量。此外,还研究了拉帕酮对前列腺癌、甲状腺癌和结直肠癌细胞系的细胞毒性活性,并与多柔比星和埃博霉素进行了比较。结果表明,20 分钟的 UAE 用乙酸乙酯或氯仿提取是最有效和经济的拉帕酮提取方法。拉帕酮对 PC3(IC = 6.50 μg/mL)、Du145(IC = 7.68 μg/mL)、FTC133(IC = 6.01 μg/mL)、8505C(IC = 7.84 μg/mL)和 Caco-2(IC = 8.79 μg/mL)细胞系在 24 小时后表现出高细胞毒性活性,对 HT29 细胞系在 48 小时后(IC = 11.67 μg/mL)也表现出高细胞毒性活性。此外,它比同源物埃博霉素或多柔比星具有更有利的安全性。获得的最佳提取参数集可用于科学和工业目的,以获得最佳的拉帕酮产量。此外,这种苯醌具有高细胞毒性活性和良好的选择性。