Center for Mitochondria and Healthy Aging, College of Life Sciences, Yantai University, Yantai, P. R. China.
School of Pharmacy, Lanzhou University, Lanzhou, P. R. China.
J Sep Sci. 2022 Jul;45(14):2435-2445. doi: 10.1002/jssc.202200040. Epub 2022 May 11.
Saxifraga atrata is an important traditional Tibetan medicine used to treat cough and pneumonia, and has tremendous medicinal potential. In this study, we devised a technique to separate 1,1-diphenyl-2-picrylhydrazyl inhibitors from a methanol extract of S. atrata. The material was first processed using MCI GEL CHP20P medium-pressure liquid chromatography, yielding 1.1 g of the target fraction Fr2. Subsequently, online hydrophilic interaction liquid chromatography-1,1-diphenyl-2-picrylhydrazyl assay was used to identify prospective 1,1-diphenyl-2-picrylhydrazyl inhibitors, and two 1,1-diphenyl-2-picrylhydrazyl inhibitor fractions (Fr24 and Fr25) were identified from Fr2. Then, medium-pressure preparation was continued using an XIon column to separate two 1,1-diphenyl-2-picrylhydrazyl inhibitor fractions (Fr24 and Fr25). The target compound was concentrated in fractions Fr24 and Fr25 using reverse-phase liquid chromatography during further separation procedures. Finally, the purity, structure, and 1,1-diphenyl-2-picrylhydrazyl inhibitory activity of the isolated 1,1-diphenyl-2-picrylhydrazyl inhibitors were determined. Two 1,1-diphenyl-2-picrylhydrazyl inhibitors (adenosine with the half maximal inhibitory concentration of 66.87 ± 14.33 μM and (-)-4-O-(E)-caffeoyl-l-threonic acid with the half maximal inhibitory concentration of 59.06 ± 5.02 μM) were isolated with purities exceeding 95%. The results showed that this technology is effective in the targeted separation of antioxidants from natural products.
绵毛楼梯草是一种重要的藏药,用于治疗咳嗽和肺炎,具有巨大的药用潜力。在本研究中,我们设计了一种从绵毛楼梯草甲醇提取物中分离 1,1-二苯基-2-苦基肼抑制剂的技术。首先,将材料用 MCI GEL CHP20P 中压液相色谱进行处理,得到 1.1g 目标部分 Fr2。随后,采用在线亲水相互作用液相色谱-1,1-二苯基-2-苦基肼测定法鉴定潜在的 1,1-二苯基-2-苦基肼抑制剂,从 Fr2 中鉴定出两个 1,1-二苯基-2-苦基肼抑制剂部分(Fr24 和 Fr25)。然后,继续使用 XIon 柱进行中压制备,以分离两个 1,1-二苯基-2-苦基肼抑制剂部分(Fr24 和 Fr25)。在进一步的分离过程中,使用反相液相色谱法将目标化合物浓缩在 Fr24 和 Fr25 部分中。最后,确定分离得到的 1,1-二苯基-2-苦基肼抑制剂的纯度、结构和 1,1-二苯基-2-苦基肼抑制活性。分离得到两种 1,1-二苯基-2-苦基肼抑制剂(半抑制浓度为 66.87±14.33μM 的腺苷和半抑制浓度为 59.06±5.02μM 的(-)-4-O-(E)-咖啡酰基-l-苏糖醇),纯度均超过 95%。结果表明,该技术可有效用于从天然产物中靶向分离抗氧化剂。