Raghavan Rahul, Cheriyamundath Sanith, Madassery Joseph
Department of Biotechnology, University of Calicut, Malappuram, Kerala, India.
Indian J Pharmacol. 2015 May-Jun;47(3):322-4. doi: 10.4103/0253-7613.157132.
To investigate the effect of DMSO on cisplatin induced cytotoxicity (invitro) against K562 (Human mylogenous leukemia) cell line and to study the cisplatin-DMSO adduct formation using UV-spectrophotometer.
Effect of DMSO on the cytotoxicity of cisplatin was studied in K562 (Chronic mylogenous leukemia) cell line by MTT assay. Cisplatin-DMSO adduct formation was studied by continuously monitoring the increase in absorption peaks for 30 minutes using UV-spectrophotometer.
0.1-0.3% DMSO markedly reduced the cytotoxic activity of cisplatin in K562 cells. Cisplatin-DMSO adduct formation was detected using UV-spectrophotometer. Continuous increase in UV absorbance between 250nm-290nm was observed when cisplatin (0.5mg/ml) and DMSO (10%) were mixed.
Present study revealed that DMSO inactivates the cytotoxicity of cisplatin. Cisplatin-DMSO mixture showed increased absorbance at 250-290nm. Therefore, using DMSO in invitro assays might result in misinterpretation of actual efficacy of drugs.
研究二甲基亚砜(DMSO)对顺铂在体外诱导的针对K562(人髓系白血病)细胞系的细胞毒性的影响,并使用紫外分光光度计研究顺铂 - DMSO加合物的形成。
通过MTT法研究DMSO对K562(慢性髓系白血病)细胞系中顺铂细胞毒性的影响。使用紫外分光光度计连续监测30分钟内吸收峰的增加,以研究顺铂 - DMSO加合物的形成。
0.1 - 0.3%的DMSO显著降低了顺铂在K562细胞中的细胞毒性。使用紫外分光光度计检测到顺铂 - DMSO加合物的形成。当顺铂(0.5mg/ml)和DMSO(10%)混合时,观察到250nm - 290nm之间的紫外吸光度持续增加。
本研究表明DMSO使顺铂的细胞毒性失活。顺铂 - DMSO混合物在250 - 290nm处显示吸光度增加。因此,在体外试验中使用DMSO可能会导致对药物实际疗效的错误解读。