Yang Ling-juan, Jiao Cheng-jin, Gao Er-quan
Zhong Yao Cai. 2015 Feb;38(2):311-4.
To establish a method to determine dencichine (β-ODAP) and its isomer (α-ODAP) in Panax notoginseng by pre-column derivatization HPLC with 1-fluoro-2,4-dinitrobenzene (FDNB).
A Luna-C18 column (250 mm x 4.6 mm, 5 µm) was used, acetonitrile- (HAc-NaAc) as the mobile phase with the ratio of 17:83, the detection wavelength was 360 nm, the column temperature was 40 °C, and 20 µL of sample was injected for HPLC analysis.
In 0.30-50.50 µg/mL,β-ODAP had a good linear relationship with peak area, A2 = 140.50C1 + 72.30, r1 = 0.9995; In 0.10-16.15 µg/mL, α-ODAP has a good linear relationship with peak area, A2 = 106.60C2 + 56.00, r2 = 0.9992.
There are appreciable β-ODAP and α-ODAP in different samples of Panax notoginseng. The method is simple, rapid, accurate and can be used for the detection of dencichine and its isomer in other samples.
建立一种采用1-氟-2,4-二硝基苯(FDNB)柱前衍生化高效液相色谱法测定三七中三七素(β-ODAP)及其异构体(α-ODAP)的方法。
采用Luna-C18柱(250 mm×4.6 mm,5 µm),以乙腈-(HAc-NaAc)为流动相,比例为17:83,检测波长为360 nm,柱温为40℃,进样量为20 µL进行高效液相色谱分析。
在0.30 - 50.50 µg/mL范围内,β-ODAP峰面积与浓度呈良好线性关系,A2 = 140.50C1 + 72.30,r1 = 0.9995;在0.10 - 16.15 µg/mL范围内,α-ODAP峰面积与浓度呈良好线性关系,A2 = 106.60C2 + 56.00,r2 = 0.9992。
不同三七样品中均含有一定量的β-ODAP和α-ODAP。该方法简便、快速、准确,可用于其他样品中三七素及其异构体的检测。