Simultaneous Estimation of Scopoletin, Bacopaside-II, Bacopasaponin-C, Withanolide-A, and Withanoside-IV in a Clinically Proven Polyherbal Formulation for Treatment of Insomnia

S. Kolhe, S. Yewale, P. Kolsure, S. Dhavale, S. Padmanabhan
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Abstract

The present work is aimed to develop and validate a reverse phase high performance liquid chromatography (RP-HPLC) method for the simultaneous estimation of Scopoletin, Bacopaside-II, Bacopasaponin-C, Withanolide-A, and Withanoside-IV in a proprietary polyherbal formulation containing Bacopa monnieri (Brahmi), Convolvulus pluricaulis (Shankhapushpi), Withania somnifera (Ashwagandha), Nardostachys jatamansi (Jatamansi), Myristica fragrans (Jatiphal) and Valeriana wallichii (Tagar) extracts intended for the treatment of insomnia. The HPLC analysis was performed on a Inertsil ODS, 3V, 250 x 4.6 mm x 5µm, C18 column using 0.1% orthophosphoric acid buffer as the mobile phase (solvent A) and acetonitrile (solvent B) with the gradient: 0-5 min, 10-20% B; 5-10 min, 20-30% B; 10-25 min, 30% B; 25-30 min, 30-40% B; 30-40 min, 40% B; 40-45 min, 40-60% B; 45-48 min, 60% B; 48-50 min, 60-30% B; 50-52 min, 30-10% B and 52-55 min, 10% B at a flow rate of 0.8 ml/min. The detection wavelength was chosen at 227 nm for Withanoside-IV and Withanolide-A, for Scopoletin, Bacopaside-II and Bacopasaponin C, it was 205 nm. The HPLC method was validated as per ICH guidelines for linearity, LOD and LOQ. The calibration curve of all the five phytomarkers showed excellent linear correlation coefficients with values (r2=0.996) for Scopoletin, (r2=0.995) for Withanoside-IV, (r2=0.996) for Withanolide-A, (r2=0.996) for Bacopaside-II and (r2=0.999) for Bacopasaponin-C. Limits of detection (LOD) were 0.04, 0.43, 0.35, 0.39 and 0.18 μg/ml and limits of quantification (LOQ) were 0.12, 1.29, 1.06, 1.18 and 0.54 μg/ml for Scopoletin, Withanoside-IV, Withanolide-A, Bacopaside-II and Bacopasaponin-C respectively. The developed HPLC method showed good separation of all the five constituents, enabling efficient analysis of Scopoletin, Withanoside-IV, Withanolide-A, Bacopaside-II, and Bacopasaponin-C in the polyherbal formulation
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同时评估东莨菪内酯、假马齿苋皂苷- ii、假马齿苋皂苷- c、Withanolide-A和withan皂苷- iv在临床证实的治疗失眠的复方制剂中的含量
本研究旨在建立一种反相高效液相色谱(RP-HPLC)方法,用于同时测定假马齿苋(Brahmi)、旋花(Shankhapushpi)、假马齿苋(Ashwagandha)、假马齿苋(jatamansi)、假马齿苋(jatamansi)、假马齿苋皂苷- ii、假马齿苋皂苷- c、假马齿苋皂苷- a和假马齿苋皂苷- iv的含量。香肉豆蔻(Jatiphal)和缬草(Tagar)提取物用于治疗失眠。HPLC色谱柱为Inertsil ODS, 3V, 250 × 4.6 mm × 5µm, C18,流动相为0.1%正磷酸缓冲液(溶剂a),乙腈(溶剂B),梯度为:0-5 min, 10-20% B;5-10分钟,20-30% B;10-25分钟,30% B;25-30分钟,30-40% B;30-40分钟,40% B;40-45分钟,40-60% B;45-48分钟,60% B;48-50分钟,60-30% B;50-52分钟,30-10% B和52-55分钟,10% B,流速为0.8 ml/min。对冬莨菪苷iv和冬莨菪内酯a的检测波长为227 nm,对东莨菪内酯、假马刀皂苷- ii和假马刀皂苷C的检测波长为205 nm。HPLC法按照ICH标准进行线性度、定量限和定量限验证。5种植物标志物的标定曲线与东莨菪碱(r2=0.996)、威皂苷iv (r2=0.995)、威皂苷a (r2=0.996)、假马齿苋皂苷- ii (r2=0.996)和假马齿苋皂苷- c (r2=0.999)均呈良好的线性相关。东莨菪内酯、威皂苷iv、威皂内酯a、马尾草皂苷- ii和马尾草皂苷- c的检出限分别为0.04、0.43、0.35、0.39和0.18 μg/ml,定量限分别为0.12、1.29、1.06、1.18和0.54 μg/ml。所建立的高效液相色谱法分离效果良好,可有效分析复方中东莨菪碱、威皂苷- iv、威皂苷- a、马齿苋皂苷- ii和马齿苋皂苷- c的成分
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