Mehrotra Deepshikha, Shetty Rajmohan Y, Shetty Jayaprakasha, Kumar B Mohana, Shetty A Veena, Shetty Shraddha, Shetty Rashmi N
Department of Pediatric and Preventive Dentistry, D.Y. Patil University School of Dentistry, Navi Mumbai, Maharashtra, India.
Department of Pediatric and Preventive Dentistry, A. B. Shetty Memorial Institute of Dental Sciences, Nitte (Deemed to be University), Deralakatte, Mangalore, Karnataka, India.
J Pharm Bioallied Sci. 2024 Jul;16(Suppl 3):S2046-S2048. doi: 10.4103/jpbs.jpbs_1293_23. Epub 2024 Apr 3.
Since the introduction of amalgam for tooth fillings, there have been concerns that mercury toxicity could pose unacceptable health risks. is an ancient medical discipline that focuses on the utilization of metals and minerals for the treatment of diseases. Nevertheless, these minerals cannot be directly administered to the human body in their natural state due to their potential adverse effects. Hence, for medicinal purposes, these metals and minerals need to undergo purification () to eliminate impurities and modify their physical, chemical, and biological characteristics.
Human gingival fibroblasts (HGF) were exposed to commercially available mercury (CA-Hg) and ayurvedically purified mercury (AP-Hg) at concentrations of 6.25 μM, 12.5 μM, 25 μM and 50 μM. The unexposed HGF cultured in basal media was considered a control. All the samples were cultured for 24 hours and 48 hours, and the cytotoxicity was analyzed by MTT assay.
Cell viability between the control and experimental groups varied at 24 hours, however, the results were not statistically significant (p>0.05). At 48 hours, cell viability was higher in the AP-Hg group as compared to the CA-Hg group at the concentration of 6.25 μM, and the difference was statistically significant (p<0.05). The cell proliferation assay results demonstrated a statistically significant difference in the mean optical density values (p<0.05) between CA-Hg and AP-Hg at 12.50 μM, 25 μM, and 50, μM concentrations observed at 24 hours. At 48 hours, a statistically significant difference in the mean OD values (p<0.05) between CA-Hg and AP-Hg at all four concentrations was observed. Conclusion: AP-Hg at a concentration of 6.25 μM demonstrated higher cell viability at 48 hours. Further, the cell proliferation rate was also higher for AP-Hg at all concentrations at 24 and 48 hours. These results indicated a less cytotoxic effect of AP-Hg than CA-Hg in HGF and hence could be employed for dental amalgam preparations.
自从汞合金被用于补牙以来,人们一直担心汞中毒会带来不可接受的健康风险。阿育吠陀医学是一门古老的医学学科,专注于利用金属和矿物质治疗疾病。然而,由于这些矿物质的潜在副作用,它们不能以天然状态直接施用于人体。因此,出于药用目的,这些金属和矿物质需要进行提纯()以去除杂质并改变其物理、化学和生物学特性。
将人牙龈成纤维细胞(HGF)暴露于浓度为6.25μM、12.5μM、25μM和50μM的市售汞(CA-Hg)和经阿育吠陀医学提纯的汞(AP-Hg)中。在基础培养基中培养的未暴露HGF被视为对照。所有样品均培养24小时和48小时,并通过MTT法分析细胞毒性。
对照组和实验组之间的细胞活力在24小时时有所不同,但结果无统计学意义(p>0.05)。在48小时时,在6.25μM浓度下,AP-Hg组的细胞活力高于CA-Hg组,差异具有统计学意义(p<0.05)。细胞增殖试验结果表明,在24小时观察到的12.50μM、25μM和50μM浓度下,CA-Hg和AP-Hg之间的平均光密度值存在统计学显著差异(p<0.05)。在48小时时,在所有四个浓度下,CA-Hg和AP-Hg之间的平均OD值均存在统计学显著差异(p<0.05)。结论:浓度为6.25μM的AP-Hg在48小时时表现出更高的细胞活力。此外,在24小时和48小时时,所有浓度的AP-Hg的细胞增殖率也更高。这些结果表明,AP-Hg对HGF的细胞毒性作用小于CA-Hg,因此可用于牙科汞合金制剂。