Mandova Tsvetelina, Audo Grégoire, Michel Sylvie, Grougnet Raphaël
Laboratory of Pharmacognosy, UMR CNRS 8638, Faculty of Pharmacy, Paris Descartes University, Sorbonne Paris Cité, 4 avenue de l'Observatoire, 75006 Paris, France; Gilson Purification SAS, 22 rue Bourseul, ZA du Poteau, 56890 Saint-Avé, France.
Gilson Purification SAS, 22 rue Bourseul, ZA du Poteau, 56890 Saint-Avé, France.
J Chromatogr A. 2017 Sep 1;1513:149-156. doi: 10.1016/j.chroma.2017.07.023. Epub 2017 Jul 8.
A purification sequence including a Gilson CPC 250 PRO device coupled to PrepHPLC hyphenated with a MS triggering fraction collector was applied to isolate secoiridoid glycosides from a complex methanolic extract of Centaurium erythraea. This species is widely used for ethnomedicinal purposes around the Mediterranean Sea. The solvent system ethyle acetate/ethanol/water 7.5/3/5 was determined using shake-flask method targeting swertiamarin, the major secoiridoid of the extract. Optimization of CPC experimental parameters enabled the injection of 4g of extract with a flow rate of 40mL/min at 3000rpm to provide a secoiridoid glycosides enriched fraction. 130mg of this latter was submitted to a second step of purification by preparative HPLC (gradient water/formic acid (19:1) (A) and methanol (B) as follows: 0min, 85% A; 8min, 60% A; 12min, 55% A; 35min, 55% A; 40min, 10% A; 50min, 10% A; 52min, 85% A; 55min, 85% A) to give swertiamarin (36mg, yield 27.7%, purity 98.2%). Other secoiridoid glycosides (sweroside, gentiopicroside, secologanol, secoxyloganin) were also isolated in minor amounts. As these monoterpene derivatives are responsible for several biological activities, their quick recovery with high yield and purity may serve as a model for further scale-up and industrial development.
采用一种纯化流程,该流程包括连接PrepHPLC并与质谱触发馏分收集器联用的吉尔森CPC 250 PRO装置,用于从红百金花的复杂甲醇提取物中分离裂环烯醚萜苷。该物种在地中海周边地区被广泛用于民族医药。使用摇瓶法以獐牙菜苦苷(提取物中的主要裂环烯醚萜)为目标,确定了乙酸乙酯/乙醇/水7.5/3/5的溶剂体系。对CPC实验参数进行优化后,能够以40mL/min的流速、3000rpm的转速进样4g提取物,以得到富含裂环烯醚萜苷的馏分。将130mg该馏分进行制备型HPLC第二步纯化(梯度洗脱,流动相为水/甲酸(19:1)(A)和甲醇(B),洗脱程序如下:0min,85% A;8min,60% A;12min,55% A;35min,55% A;40min,10% A;50min,10% A;52min,85% A;55min,85% A),得到獐牙菜苦苷(36mg,产率27.7%,纯度98.2%)。还分离出了少量其他裂环烯醚萜苷(獐牙菜苷、龙胆苦苷、裂环醇、裂环马钱子苷)。由于这些单萜衍生物具有多种生物活性,它们的高收率和高纯度快速回收可为进一步扩大规模和工业化发展提供一个模型。