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采用高效液相色谱法,以环糊精作为流动相添加剂,同时分析了积雪草中的五种三萜。

Simultaneous analysis of five triterpenes in Centella asiatica by high performance liquid chromatography with cyclodextrins as the mobile phase additives.

机构信息

Shaanxi Institute for Food and Drug Control, No 21, Keji Fifth Road, Xi'an, 710065, Shaanxi Province, China.

Nanjing Aureole Pharmaceutical Co., Ltd., No.11, Changchun Road, High Tech Zone, Zhengzhou, 450001, Henan Province, China.

出版信息

Sci Rep. 2020 Oct 29;10(1):18577. doi: 10.1038/s41598-020-75554-z.

Abstract

Triterpenes are considered the major active components in Centella asiatica (L.) Urb. (C. asiatica), such as asiatic acid, madecassic acid, asiaticoside, madecassoside and asiaticoside B. It is difficult to simultaneously determine five triterpenes because of madecassoside isomers (madecassoside and asiaticoside B), and the great polarity difference between triterpene acid and triterpene glycoside. In this study, a simple high performance liquid chromatography method with isocratic elution employing cyclodextrins (CDs) as the mobile phase additives was developed to determine five triterpenes in C. asiatica. Various factors affecting triterpenes retention in the C18 column, such as the nature of CDs, γ-CD concentration, acetonitrile percentage and temperature, were studied. Experimental results showed that γ-CD, as an effective mobile phase additive, could markedly reduce the retention of triterpenes (especially asiatic acid and madecassic acid), and improve the separation for madecassoside and asiaticoside B. The elution of five triterpenes could be achieved on an ODS C18 column within 30 min using the acetonitrile-0.2% phosphoric acid contained 4.0 mM γ-CD (20:80, v/v) mixture as the mobile phase. The retention modification of triterpenes may be attributed to the formation of the triterpenes-γ-CD inclusion complexes. The optimized method was successfully applied for simultaneous determination of five triterpenes in C. asiatica.

摘要

三萜类化合物被认为是积雪草(Centella asiatica (L.) Urb.)(C. asiatica)中的主要活性成分,如积雪草酸、积雪草苷、羟基积雪草苷、积雪草苷 B 等。由于积雪草酸异构体(积雪草酸和羟基积雪草苷 B)和三萜酸与三萜糖苷之间的巨大极性差异,很难同时测定五种三萜类化合物。在这项研究中,开发了一种简单的高效液相色谱法,采用环糊精(CDs)作为流动相添加剂进行等度洗脱,以测定积雪草中的五种三萜类化合物。研究了影响 C18 柱中三萜类化合物保留的各种因素,如 CDs 的性质、γ-CD 浓度、乙腈百分比和温度等。实验结果表明,γ-CD 作为一种有效的流动相添加剂,可以显著降低三萜类化合物(尤其是积雪草酸和积雪草苷)的保留,改善积雪草酸苷和羟基积雪草苷 B 的分离效果。使用乙腈-0.2%磷酸(含 4.0mM γ-CD,20:80,v/v)混合物作为流动相,在 ODS C18 柱上可在 30 分钟内洗脱五种三萜类化合物。三萜类化合物的保留修饰可能归因于三萜类化合物-γ-CD 包合物的形成。优化后的方法成功应用于积雪草中五种三萜类化合物的同时测定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/7596059/17489b63790e/41598_2020_75554_Fig1_HTML.jpg

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