Evidence map›Paper›PMID 31836776›Full record

ArticleScientific reports2019

A microemulsion high-performance liquid chromatography (MELC) method for the separation and determination of hydrolyzed tenuifolin in Radix Polygalae.

Hui Yan, Zhuan-Di Zheng, Hong-Fei Wu, Xiao-Chuang Liu, An Zhou

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Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Hui YanDepartment of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui, 230012, P. R. China.
Zhuan-Di ZhengDepartment of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui, 230012, P. R. China.
Hong-Fei WuDepartment of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui, 230012, P. R. China. wuhongfei2009@126.com.
Xiao-Chuang LiuThe First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, 230026, P. R. China.
An ZhouDepartment of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui, 230012, P. R. China. anzhou@ahtcm.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tenuifolin was used as a reliable chemical marker for the quality control of Radix Polygalae. The determination of tenuifolin is challenging because the analyte molecule lacks a suitable chromophore. The aim of this study was to establish a microemulsion high-performance liquid chromatography (MELC) method which is robust and sensitive, and can separate and determine tenuifolin in Radix Polygalae using an oil-in-water (O/W) microemulsion mobile phase. The separations were performed on a C18 (4.6 × 250 mm, 5 μm) column at 25 °C using a flow rate of 1.0 mL/min, and an ultraviolet detection wavelength of 210 nm. The microemulsion mobile phase comprised 2.8% (w/v) sodium dodecyl sulfate (SDS), 7.0% (v/v) n-butanol, 0.8% (v/v) n-octane and 0.1% (v/v) aqueous orthophosphate buffer (H3PO4). The linearity analysis of tenuifolin showed a correlation coefficient of 0.9923 in the concentration range of 48.00-960.00 µg/mL. The accuracy of the method based on three concentration levels ranged from 96.23% to 99.28%; the limit of detection (LOD) was 2.34 µg/mL, and the limit of quantification (LOQ) was 6.76 µg/mL. The results of our study indicated that the optimized MELC method was sensitive and robust, and can be widely applied for the separation and determination of tenuifolin in Radix Polygalae.

Indexed as

Chromatography, High Pressure LiquidDiterpenes, KauraneDrugs, Chinese HerbalEmulsionsSaponins1-ButanolBuffersGreen Chemistry TechnologyLimit of DetectionLinear ModelsOctanesParticle SizePhosphatesPlant RootsPolygalaQuality Control1-ButanolBuffersDiterpenes, KauraneDrugs, Chinese HerbalEmulsionsoctaneOctanesPhosphatesSaponinsSodium Dodecyl SulfateSurface-Active Agentstenuifolic saponintenuifolin diterpeneyuan zhiyuanzhi-1

Identifiers

PMID31836776
PMCPMC6910981

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