Therapeutic potential of novel tin metal complex of embelin isolated from Embelia ribes fruits.

IF 1.4 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Indian Journal of Pharmacology Pub Date : 2025-05-01 Epub Date: 2025-07-09 DOI:10.4103/ijp.ijp_678_23
Ruchi Singh, Durga K Mewara
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引用次数: 0

Abstract

Background: Dried Embelia ribes berries can be used to extract Embelin (2,5-Dihydroxy-3-undecylcyclohexa-2,5-diene -1,4-dione), a herbal p-benzoquinone derived from general quinones. This plant shows potential for scientific study that could provide cutting-edge therapeutic compounds. Prior studies have shown that the molecule's transformation into a complex may have increased its bioactivity. Furthermore, it has been shown that inorganic complexes are more versatile than pure organic molecules, which may improve the ability to target sites that are commonly present in the aquatic ecological environment.

Materials and methods: One of the substances with known activity found in the fruits of Embelia ribes, embelin (2, 5-dihydroxy-3- undecyl-p-benzoquinone), was extracted using chloroform solvent and then separated using column chromatography techniques. An Embelin-Sn complex was created using the purified Embelin. The Embelin-Sn complex was synthesized under simple, appropriate conditions that employed room temperature. Using elemental analysis, infrared spectroscopy, mass spectrum analysis, and Proton Nuclear Magnetic Resonance (1H NMR) spectroscopy, the structure of the Embelin-Sn complex has been ascertained.

Results: The phytochemical embelin isolated from Embelia ribes was used to synthesize Embelin-Sn complex, its characterization studied, and its anticancer potential evaluated using the MTT assay and apoptotic assay on the T-47D breast cancer cell line and antibacterial study by disc diffusion method. Sn complex concentration on breast cancer cells (T-47D cell line) were exposed to varied concentrations for 24 hours, including 40, 60, 80, 100, and 120 mg/ml. This result implies that embelin inhibits the proliferation of breast cancer cells. The antibacterial property was determined by measuring the disc's inhibitory zone size.

Conclusion: For the first time, an Embelin-Sn complex was synthesized, and it exhibited zone of inhibition against E. coli and dose-dependent administration of Embelin-Sn complex represents a potential novel strategy which can successfully treat the breast cancer.

从荔枝果实中分离的新型锡金属配合物的治疗潜力。
背景:风干的南红莓可用于提取南红素(2,5-二羟基-3-十一基环己-2,5-二烯-1,4-二酮),这是一种从一般醌类中提取的草本对苯醌。这种植物显示出科学研究的潜力,可以提供尖端的治疗化合物。先前的研究表明,分子转化为复合物可能增加了其生物活性。此外,已有研究表明,无机配合物比纯有机分子更具通用性,这可能提高了靶向水生生态环境中常见位点的能力。材料与方法:用氯仿溶剂提取牛油果中已知活性物质之一的牛油果素(2,5 -二羟基-3-十一烷基-对苯醌),然后用柱层析技术分离。用纯化的Embelin制备了一个Embelin- sn复合物。在简单、适宜的室温条件下合成了Embelin-Sn配合物。利用元素分析、红外光谱、质谱分析和质子核磁共振(1H NMR)谱,确定了Embelin-Sn配合物的结构。结果:利用从Embelia ribes中分离得到的植物化学栓塞素合成了embelin - sn复合物,对其进行了表征,并通过MTT实验和凋亡实验对其进行了抗癌潜力评价,并通过圆盘扩散法对其进行了抑菌研究。将Sn复合物浓度分别为40、60、80、100、120 mg/ml,作用于乳腺癌细胞(T-47D细胞系)24小时。这一结果表明,栓塞抑制乳腺癌细胞的增殖。通过测定其抑菌带大小来确定其抑菌性能。结论:首次合成了一种对大肠杆菌具有抑制作用的Embelin-Sn复合物,剂量依赖性给药是一种潜在的治疗乳腺癌的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
4.20%
发文量
53
审稿时长
4-8 weeks
期刊介绍: Indian Journal of Pharmacology accepts, in English, review articles, articles for educational forum, original research articles (full length and short communications), letter to editor, case reports and interesting fillers. Articles concerning all aspects of pharmacology will be considered. Articles of general interest (e.g. methods, therapeutics, medical education, interesting websites, new drug information and commentary on a recent topic) are also welcome.
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