Simultaneous Quantification of Acid chlorogenic, Acid caffeic and Rutin in Herba Siegesbeckiae orientalis by HLPC Method

Tran Thi Van Anh, Pham Quoc Tuan, N. Van Khanh, Dao Viet Hung, Nguyen Thi Thanh Hai, Tran Van Thao, Nguyen Thi Hong Nhung, Ngo Thi Xuan Thinh, Ha Thanh Hoa, Nguyen Xuan Truong
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Abstract

Herba Siegesbeckiae is a medicinal material derived from the aerial part of Siegesbeckia orientalis, which is used to treat various types of pain such as back, knees, bones, joints, and numbness of limbs. This plant contains several phenolic compounds, including chlorogenic acid (1), caffeic acid (2), and rutin (3). They were chosen as marker compounds to develop a quantification method. In this study, a high-performance liquid chromatography (HPLC) method with a DAD detector was used to simultaneously quantify these three compounds (1-3). The Agilent C18 column (250 x 4.6 mm; 5 µm) was used for the separation of the analytes, and the mobile phase consisted of MeCN - 0.1% phosphoric acid in water with gradient elution. The flow rate was 1.0 ml/min, and the detection wavelength was 320 nm for 1 and 2, and 360 nm for 3. The injection volume was 20 µl. The method was validated according to the guidelines of ICH and AOAC on system suitability, specificity, linearity, precision, and accuracy. The established quantification method was applied to determine the content of compounds 1, 2, and 3 in samples of Herba Siegesbeckiae, which were found to be 0.09-0.82 mg/g, 0.02-0.21 mg/g, 0.07-0.52 mg/g, respectively. This quantification method can be used to assess the quality of Herba Siegesbeckiae and related products.
高效液相色谱法同时测定白荆中绿原酸、咖啡酸和芦丁的含量
茜草是一种从东方茜草属植物的地上部分提取的药材,用于治疗各种类型的疼痛,如背部、膝盖、骨骼、关节和四肢麻木。该植物含有多种酚类化合物,包括绿原酸(1),咖啡酸(2)和芦丁(3)。选择它们作为标记化合物建立定量方法。本研究采用DAD检测器的高效液相色谱(HPLC)方法同时定量了这三种化合物(1-3)。Agilent C18色谱柱(250 x 4.6 mm;色谱柱为5µm),流动相为MeCN - 0.1%磷酸,梯度洗脱。流速为1.0 ml/min, 1、2检测波长为320 nm, 3检测波长为360 nm。进样量为20µl。根据ICH和AOAC的指南对该方法进行了系统适用性、特异性、线性度、精密度和准确度的验证。采用所建立的定量方法对菝葜样品中化合物1、2、3的含量进行测定,其含量分别为0.09 ~ 0.82 mg/g、0.02 ~ 0.21 mg/g、0.07 ~ 0.52 mg/g。该定量方法可用于百叶草及相关产品的质量评价。
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