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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Strategy for the separation of strongly polar antioxidant compounds from Lycium barbarum L. via high-speed counter-current chromatography
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Strategy for the separation of strongly polar antioxidant compounds from Lycium barbarum L. via high-speed counter-current chromatography

机译:通过高速逆流色谱法分离强极性抗氧化化合物的策略

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In the separation of strongly polar antioxidant compounds from natural products using high-speed counter-current chromatography that is target-guided by 2,2-diphenyl-1-picrylhydrazyl high-performance liquid chromatography experimentation, low adsorption ability is encountered due to the strong polarity of the target compounds. In this study, a strategy of novel partition coefficient value calculation was proposed for overcoming this problem. The partition coefficient value was expressed as the ratio of the antioxidant activities of the upper phase and the lower phase. This strategy was used in high-speed counter-current chromatography with a hydrophilic organic/salt-containing aqueous two-phase system for bioassay-guided separation of strongly polar antioxidant compounds from Lycium barbarum L. The antioxidant activity was determined via the radical scavenging activity method using 2,2-diphenyl-1-picrylhydrazyl radicals. A hydrophilic organic/salt-containing aqueous two-phase system of 95% EtOH - sat. (NH4)(2)SO4 (1:1.8, v/v) was successfully used to separate Lycium barbarum L. extract. Five fractions were collected via high-speed counter-current chromatography separation. The antioxidant activity of the third fraction was the highest. Three compounds were separated via MCl gel column chromatography and Sephadex LH-20 column chromatography from the third fraction, and their antioxidant activities were determined. The antioxidant activities of the three compounds were higher than that of the third fraction. These results demonstrate that this strategy can be used to separate strongly polar antioxidant compounds from natural products.
机译:在使用靶标引导的高速逆流色谱法由2,2-二苯基-1-富铬酰基高性能液相色谱实验的高速逆流色谱分离的强极性抗氧化剂化合物的分离在2,2-二苯基-1-富铬酰基高性能液相色谱实验中,由于强劲而遇到低吸附能力目标化合物的极性。在本研究中,提出了一种新的分区系数值计算策略,以克服这个问题。分配系数值表示为上阶段和下阶段的抗氧化活性的比率。该策略用于高速反电流色谱法,其具有亲水性有机/盐的水性两相体系,用于来自枸杞L枸杞的强极性抗氧化化合物的生物测定的分离。通过自由基清除活性测定抗氧化活性使用2,2-二苯基-1-富铬基酰基自由基的方法。含有95%EtOH-SAT的亲水性有机/盐水性两相体系。 (NH4)(2)SO 4(1:1.8,v / v)成功地用于分离枸杞L.提取物。通过高速逆流色谱分离收集五个级分。第三部分的抗氧化活性是最高的。通过MCl凝胶柱色谱分离三种化合物,并从第三部分中分离Sephadex LH-20柱色谱,测定它们的抗氧化活性。三种化合物的抗氧化活性高于第三部分。这些结果表明,该策略可用于将强极性抗氧化剂与天然产物分离。

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