Abstract

Lignans, which are recognized as main constituents in Justicia procumbens, have attracted considerable attention due to their pharmacological activities, including antitumor, anti-hepatitic, cytotoxic, anti-microbial, and anti-virus properties. Preparative high-speed counter-current chromatography (HSCCC) was successfully applied to the isolation and purification of four lignans (justicidin B (1), justicidin A (2), 6'-hydroxyjusticidin C (3) and lignan J1 (4)) from J. procumbens using stepwise elution with a pair of two-phase solvent systems composed of n-hexane–ethyl acetate–methanol–water at (1.3:1:1.3:1, v/v) and (2.5:1:2.5:1, v/v). The preparative HSCCC separation was performed on 300 mg of crude sample yielding compounds 1 (19.7 mg), 2 (9.86 mg), 3 (11.26 mg), and 4 (2.54 mg) in a one-step separation, with purities over 95% as determined by HPLC. The structures of these compounds were identified by MS, 1H-NMR and 13C-NMR. This is the first report on the application of HSCCC to the efficient separation of lignans from J. procumbens.

Highlights

  • Justicia procumbens (Acanthaceae), known as “Juechuang” in Chinese, is one of the most popular traditional Chinese medicines (TCMs) used to treat fever, pain, and cancer [1,2,3]

  • The present paper describes the successful preparative separation and purification in one-step of the four lignans justicidin B (1), justicidin A (2), 6'-hydroxyjusticidin C (3) and lignan J1 (4) (Figure 1) from a crude sample of J. procumbens using high-speed counter-current chromatography (HSCCC) in stepwise elution mode for the first time

  • The stepwise elution mode consisted of a pair of two-phase solvent systems composed of n-hexane-ethyl acetate-methanol-water at different ratios

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Summary

Introduction

Justicia procumbens (Acanthaceae), known as “Juechuang” in Chinese, is one of the most popular traditional Chinese medicines (TCMs) used to treat fever, pain, and cancer [1,2,3]. In the past few years, the bioactive principles isolated from J. procumbens were identified as arylnaphthalide and diarylbutane lignans, and their glycosides [10,11,12]. They exhibit antitumor [13], anti-hepatitis [14], cytotoxic [15], anti-microbial [16], and antiviral activities [17]. This motivated us to develop an efficient preparation method for the bioactive lignans

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