Diab Kawthar A E, Shafik Reham Ezzat, Yasuda Shin
Genetics and Cytology Department, National Research Centre, Cairo, Egypt E-mail :
Asian Pac J Cancer Prev. 2015;16(16):7053-60. doi: 10.7314/apjcp.2015.16.16.7053.
In the present work, novel orange peel was extracted with 100%EtOH (ethanol) and fractionated into four fractions namely F1, F2, F3, F4 which were eluted from paper chromatographs using 100%EtOH, 80%EtOH, 50%EtOH and pure water respectively. The crude extract and its four fractions were evaluated for their total polyphenol content (TPC), total flavonoid content (TFC) and radical scavenging activity using DPPH (1,1-diphenyl-2-picrylhydrazyl) assay. Their cytotoxic activity using WST assay and DNA damage by agarose gel electrophoresis were also evaluated in a human leukemia HL-60 cell line. The findings revealed that F4 had the highest TPC followed by crude extract, F2, F3 and F1. However, the crude extract had the highest TFC followed by F4, F3, F2, and F1. Depending on the values of EC50 and trolox equivalent antioxidant capacity, F4 possessed the strongest antioxidant activity while F1 and F2 displayed weak antioxidant activity. Further, incubation HL-60 cells with extract/fractions for 24h caused an inhibition of cell viability in a concentration- dependent manner. F3 and F4 exhibited a high antiproliferative activity with a narrow range of IC50 values (45.9 - 48.9 μg/ml). Crude extract exhibited the weakest antiproliferative activity with an IC50 value of 314.89 μg/ml. Analysis of DNA fragmentation displayed DNA degradation in the form of a smear-type pattern upon agarose gel after incubation of HL-60 cells with F3 and F4 for 6 h. Overall, F3 and F4 appear to be good sources of phytochemicals with antioxidant and potential anticancer activities.
在本研究中,用100%乙醇提取新鲜橙皮,并将其分成四个部分,即F1、F2、F3、F4,它们分别用100%乙醇、80%乙醇、50%乙醇和纯水从纸色谱中洗脱。使用DPPH(1,1-二苯基-2-苦基肼)法评估粗提物及其四个部分的总多酚含量(TPC)、总黄酮含量(TFC)和自由基清除活性。还在人白血病HL-60细胞系中使用WST法评估了它们的细胞毒性活性以及通过琼脂糖凝胶电泳评估DNA损伤。研究结果显示,F4的TPC最高,其次是粗提物、F2、F3和F1。然而,粗提物的TFC最高,其次是F4、F3、F2和F1。根据半数有效浓度(EC50)值和Trolox等效抗氧化能力,F4具有最强的抗氧化活性,而F1和F2表现出较弱的抗氧化活性。此外,将HL-60细胞与提取物/部分孵育24小时会导致细胞活力呈浓度依赖性抑制。F3和F4表现出高抗增殖活性,IC50值范围较窄(45.9 - 48.9μg/ml)。粗提物表现出最弱的抗增殖活性,IC50值为314.89μg/ml。DNA片段化分析显示,在将HL-60细胞与F3和F4孵育6小时后,琼脂糖凝胶上呈现出涂片型模式的DNA降解。总体而言,F3和F4似乎是具有抗氧化和潜在抗癌活性的植物化学物质的良好来源。