ZHANG Yan-jun, LIAO Ri-quan, ZHENG Yun-yun, YIN Yan-zhen, HUANG Qiu-yuan, XU Guo-xin, HUANG En-jiao, ZHU Jing-qing, WU Cai-li. Optimization of Extraction Technology on Antioxidants in Vitro from Pitaya Flower and Evaluation of Anti-inflammatory Activities[J]. Science and Technology of Food Industry, 2018, 39(18): 137-142. DOI: 10.13386/j.issn1002-0306.2018.18.025
Citation: ZHANG Yan-jun, LIAO Ri-quan, ZHENG Yun-yun, YIN Yan-zhen, HUANG Qiu-yuan, XU Guo-xin, HUANG En-jiao, ZHU Jing-qing, WU Cai-li. Optimization of Extraction Technology on Antioxidants in Vitro from Pitaya Flower and Evaluation of Anti-inflammatory Activities[J]. Science and Technology of Food Industry, 2018, 39(18): 137-142. DOI: 10.13386/j.issn1002-0306.2018.18.025

Optimization of Extraction Technology on Antioxidants in Vitro from Pitaya Flower and Evaluation of Anti-inflammatory Activities

  • To investigate the optimum technology for extraction of antioxidants and the extracts' anti-inflammatory activity from pitaya flower, the antioxidant activity in vitro of the extracts from pitaya flower was determined by scavenging capacity of DPPH·and·OH.The effects of extraction temperature, solid-liquid ratio, extraction time and ethanol concentration were studied through the single factor experiments, and L9 (34) orthogonal test was used to explore the antioxidant activities of extracts from pitaya flower in vitro. The results showed that, the optimized conditions were:70% ethanol, the solid-liquid ratio of 1:30 g/mL, when treatment time was 3.0 h at 75℃. Under these optimized conditions, the IC50 for scavenging capacity of the extracts against DPPH·and·OH were 0.273, 0.288 mg/mL, respectively. And within a certain range, the higher the concentration of the crude extract, the better its antioxidant activity, which had an obviously dose-effect relationship. Moreover the extracts under the optimized conditions could decrease secretions of NO in LPS-induced RAW264.7 macrophage cells, and the anti-inflammatory activity for the extracts increased in a concentration-dependent manner with IC50 value of 13.94 μg/mL. The extracts had good antioxidant activity and anti-inflammatory activity in vitro.
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