Jing Siqun, Zhang Xiaoming, Yue Li
1State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Lihu Road, Wuxi, Jiangsu, China / College of Life Sciences and Technology, Xinjiang University, Shengli Road 14, Urumqi, Xinjiang, China.
State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Lihu Road, Wuxi, Jiangsu, China.
Pak J Pharm Sci. 2015 Jan;28(1 Suppl):383-91.
The objective of the present study was to evaluate an efficient purifying process of Kunlun Chrysanthemum procyanidins (KCPC) by combination of AB-8 macroporous adsorption resin and silica gel column through adsorption and desorption experiments under static and dynamic status with the purity of procyanidins and the antioxidant activity as indexes respectively. The optimum parameters for adsorption by AB-8 resin were as follows: Sample concentration 1mg/mL, pH6, injecting velocity 2 bed volume (BV) /h, with 3 BV 70% ethanol as eluting solvent, and elution flow rate 2BV /h. One cycle after treatment using AB-8 resin, the purity of KCPC obviously enhanced 3 times compared with that of not prepurified, that is from 22.68 to 63.76%. The optimum parameters for adsorption by silica gel column were as follows: The concentration of procyanidins in a sample solution of 1.2mg/mL (pH 6) with a speed of 2BV/h. Concentration for desorption, with 5 BV of 80% ethanol as an eluent at a flow rate of 2 BV/h. After one-run treatment with silica gel column, the purity of KCPC increased from 63.76 to 81.97%. The antioxidant activities of the purified KCPC in vitro were further investigated. The results indicated that the purification method of combination of AB-8 resin and silica gel column was superior to AB-8 adsorption resin used alone in term of antioxidant activities. Moreover, the 1,1-diphenyl-2-picrylhydrazyl (DPPH•) scavenging ability, the scavenging activity of hydroxyl radicals and the reducing ability appeared to be dose-dependent of KCPC. The novel purification method of combination of AB-8 resin and silica gel column will offer a promising way to purify KCPC for wider application.
本研究的目的是通过AB - 8大孔吸附树脂和硅胶柱相结合的方式,分别以原花青素的纯度和抗氧化活性为指标,通过静态和动态吸附与解吸实验,评估昆仑菊花原花青素(KCPC)的高效纯化工艺。AB - 8树脂吸附的最佳参数如下:样品浓度1mg/mL,pH6,进样速度2床体积(BV)/h,以3 BV 70%乙醇为洗脱剂,洗脱流速2BV /h。使用AB - 8树脂处理一个循环后,KCPC的纯度比未预纯化时明显提高了3倍,即从22.68%提高到63.76%。硅胶柱吸附的最佳参数如下:样品溶液中原花青素浓度为1.2mg/mL(pH 6),流速为2BV/h。解吸浓度,以5 BV 80%乙醇为洗脱剂,流速为2 BV/h。用硅胶柱进行一次处理后,KCPC的纯度从63.76%提高到81.97%。进一步研究了纯化后的KCPC的体外抗氧化活性。结果表明,AB - 8树脂和硅胶柱相结合的纯化方法在抗氧化活性方面优于单独使用AB - 8吸附树脂。此外,1,1 - 二苯基 - 2 - 苦基肼(DPPH•)清除能力、羟基自由基清除活性和还原能力似乎与KCPC呈剂量依赖性。AB - 8树脂和硅胶柱相结合的新型纯化方法将为纯化KCPC以实现更广泛应用提供一条有前景的途径。