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从山柑(Forsk.)Edgew. 中分离出的β-谷甾醇三酸酯的体外细胞毒性活性。

In-vitro cytotoxic activity of β-Sitosterol triacontenate isolated from Capparis decidua (Forsk.) Edgew.

机构信息

Department of Quality Assurance & Natural Products, PDM College of Pharmacy, Bahadurgarh, India.

出版信息

Asian Pac J Trop Med. 2012 Mar;5(3):225-30. doi: 10.1016/S1995-7645(12)60029-7.

DOI:10.1016/S1995-7645(12)60029-7
PMID:22305789
Abstract

OBJECTIVE

To study the isolation and characterization of the constituent responsible for the cytotoxic activity of the ethanolic extract of stem of Capparis decidua (C. decidua).

METHODS

The preliminary cytotoxic effect of isolated compound (β-Sitosterol triacontenate) was investigated by MTT assay on A549 solid tumor cells.

RESULTS

IC(50) value of the β-Sitosterol triacontenate was found to be 1 μM. The cytotoxic activity increased in a dose dependent manner in case of β-Sitosterol triacontenate.

CONCLUSIONS

The data therefore provide direct evidence for the role of β-Sitosterol triacontenate as a potent antimetastatic agent, which can markedly inhibit the metastatic and invasive capacity of malignant cells.

摘要

目的

研究负责山木鳖茎乙醇提取物细胞毒性的成分的分离和鉴定。

方法

通过 MTT 法测定分离得到的化合物(β-谷甾醇三酸酯)对 A549 实体瘤细胞的初步细胞毒性作用。

结果

β-谷甾醇三酸酯的 IC50 值为 1 μM。β-谷甾醇三酸酯的细胞毒性活性呈剂量依赖性增加。

结论

因此,数据为β-谷甾醇三酸酯作为一种有效的抗转移剂提供了直接证据,它可以显著抑制恶性细胞的转移和侵袭能力。

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