首页> 外文期刊>Annals of King Edward Medical University. >In Vitro Cytotoxic Potential of Plant Terpenes and Selected Medicinal Plants of Pakistan against NIH 3T3 Cell Line.
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In Vitro Cytotoxic Potential of Plant Terpenes and Selected Medicinal Plants of Pakistan against NIH 3T3 Cell Line.

机译:巴基斯坦植物萜烯和部分药用植物对NIH 3T3细胞系的体外细胞毒性潜力。

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Background: Medicinal plants are used in anticancer therapies from ages. The very first time we have not only screened anticancer medicinal plants from Pakistan but also identified anticancer plant terpenes. This study will definitely pave the way towards anticancer drug development after animal trials. Materials and Methods | This study was based on ethanolic extraction of fruits/seed of 25 plants. The cytotoxic potential of extracts and plant terpenes was evaluated against mouse fibroblasts (NIH 3T3) cell line by using MTT (3- [4, 5-dimethylthiazole-2-yl]-2, 5-diphenyl-tetrazolium bromide) assay and compared with cyclohexamide. Results | Ethanolic extracts were nontoxic against NIH3T3 cell line. On the basis of the % inhibition plants were graded as B.lycium, 48% T.bellerica, 47% C.verum, 45% Z.tenuior, 39% H. adenophyllum, 38% C. carandas, 31% C.behen, 29% P. juliflora, 28% & P.granatum, 28% W.somnifera, 27% E.cheiri, 26% S. potatorum, 24% & M.incana, 24% D. peregrina, 21% & B.lanzan, 21% L. maldivica, 20% F. lyrata, 18% F.arabica, 16% & R. indica, 16% C.absus, 13% & C.paniculatus, 13%. C. diurnum, 12% J.mimosifolia, 11% D.malabarica, 8% C. speciosa, 3% as compared to the reference drug Cyclohexamide, 70%. Whereas the maximum % inhibition was exhibited by n-Hexadecanoic acid (88%), followed by Hexadecanoic acid, methyl ester (16%) and Methyl decanoate displayed 11%. C50 of n-Hexadecanoic acid and Cyclohexamide was 3.1±0.2 and 0.8±0.2 respectively. Conclusion| Plant extracts and terpenes was found to be inactive against 3T3 cell line.
机译:背景:药用植物自古以来就被用于抗癌治疗。我们不仅是第一次从巴基斯坦筛选了抗癌药用植物,而且还鉴定了抗癌植物萜烯。这项研究无疑将为动物试验后的抗癌药物开发铺平道路。材料和方法|这项研究基于乙醇提取25种植物的果实/种子。通过使用MTT(3- [4,5-二甲基噻唑-2-基] -2,5-二苯基四唑鎓溴化物)测定评估提取物和植物萜烯对小鼠成纤维细胞(NIH 3T3)细胞系的潜在细胞毒性,并与环己酰胺。结果乙醇提取物对NIH3T3细胞系无毒。根据抑制百分数,将植物分为枸杞,48%>百日草,47%>百里香,45%> Z.tenuior,39%>腺扁豆,38%> car。 31%>山茱C,29%>桔梗,28%颗粒和石榴,28%苦瓜,27%>埃里希氏菌,26%>马铃薯,24%和inc.incana,24% > D. peregrina,21%&B.lanzan,21%>马尔代夫L.,20%> lyrata,18%> F.arabica,16%&R.indica,16%> C.absus,13%& C.paniculatus,13%。 > C. diurnum,12%> J.mimosifolia,11%> D.malabarica,8%> C. speciosa,3%,而参考药物环己酰胺为70%。正十六烷酸(88%)表现出最大的抑制率,其次是十六烷酸,甲酯(16%)和癸酸甲酯表现出11%的抑制率。正十六烷酸和环己酰胺的C50分别为3.1±0.2和0.8±0.2。结论|发现植物提取物和萜烯对3T3细胞系无活性。

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