从坦帕巴达克(Voacanga foetida (Blume) Rolfe)树皮二氯甲烷馏分中分离生物碱并测试其对 T47D 细胞株的细胞毒活性

Adriani Susanty, Nurdina Putri, Ihsan Ikhtiarudin, Novia Sinata, Dira Dira, F. Wahyuni, Dachriyanus Dachriyanus
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引用次数: 0

摘要

癌症是卫生部门面临的一个问题,因为这种疾病的发病率和死亡率都在不断上升。虽然治疗过程中仍会产生一些药物副作用,给癌症患者带来不适。产生副作用的原因是大多数抗癌药物的作用是非选择性的。由于上述一些问题,有必要鼓励寻找治疗癌症的替代药物。Voacanga foetida (Blume) Rolfe(天南星科)是 Voacanga 属的一种植物,被称为西苏门答腊的 tampa badak。众所周知,这种植物是吲哚生物碱和双吲哚生物碱的来源,具有作为抗癌药物的潜力。因此,在这项研究中,我们有兴趣探索这种植物作为天然产品来源的潜在细胞毒性活性。研究从分离过程开始,然后对分离出的化合物进行表征,最后测试它们对 T47D 乳腺癌细胞系的细胞毒活性。生物碱化合物的分离过程包括酸碱提取、液液分馏和柱层析。然后,通过盐水虾致死试验(BSLT)法和 MTT 法评估了分离物的细胞毒性活性。利用光谱分析(包括紫外光谱和傅立叶变换红外光谱)对三个分离生物碱(VFB-DB1.1、VFB-DB2.1 和 VFB-DB2.2)的结构进行了描述。其中一个分离化合物(VFB-DB1.1)还利用 1H NMR 光谱进行了表征。根据所分离化合物的 1H NMR 光谱与文献的相似性,化合物 VFB-DB1.1 被确定为voacangine。随后,BSLT 和 MTT 检测结果表明,VFB-DB1.1 对鲑鱼蒿(Artemia salina L.)的半数致死浓度(LC50)为 15.8 µg/mL,对 T47D 乳腺癌细胞的半数致死浓度(IC50)为 8.9 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。
Isolation and Cytotoxic Activity Test of Alkaloids from Dichloromethane Fraction of Bark of Tampa Badak (Voacanga foetida (Blume) Rolfe) Against T47D Cell Line
Cancer is a problem in the health sector because this disease has an increasing incidence of morbidity and mortality. While the treatment still leaves some drug side effects, which cause discomfort for cancers sufferers. The arises because most cancer drugs work non-selectively. Because of some of the problems above, it is necessary to encourage the search for alternative drugs treatment of cancer. Voacanga foetida (Blume) Rolfe (Apocynaceae) is a species of plant from the genus Voacanga known as the tampa badak from West Sumatra. This plant is known to be source of indole alkaloids and also bis-indole alkaloids potential as cancer drugs. Therefore, in this study we are interested to explore the potency of this plant as natural product sources with potential cytotoxic activity. The study was started from the isolation process and continued by characterization of the isolated compounds and then testing their cytotoxic activity T47D breast cancer cell line. The isolation process of alkaloid compounds were performed by acid-base extraction, liquid-liquid fractionation, and followed by separation using column chromatography. Then,the potency of cytotoxic activity of the isolates were screened through Brine Shrimp Lethality Test (BSLT) method and evaluated by MTT assay. The structure of three isolated alkaloids (VFB-DB1.1; VFB-DB2.1; and VFB-DB2.2) were charachterized using spectroscopic analyses, including UV and FT-IR. One isolated compound (VFB-DB1.1) was also characterized using 1H NMR spectroscopy. Based on the similarity of 1H NMR spectra of isolated compound when compared with the literature, compound VFB-DB1.1 was identified as voacangine. Then, the BSLT and MTT assay result showed that VFB-DB1.1 exhibited LC50 value of 15.8 µg/mL againt Artemia salina L.and IC50 value of 8.9 µg/mL against T47D breast cancer cells, respectively.
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