hplc同时测定阿育吠陀配方âÂÂDashmulaâÂÂ和牛膝草乙酸乙酯提取物中芹菜素和木犀草素含量的方法验证与建立

Attarde Dl, Pal Sc, Bhambar Rs
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The ethyl acetate extract of P. integrifolia (PI-ET), ‘Dashmularishtha’: Manufactuer 1; 3 coded batches as DF1, DF2, DF3, Manufacturer 2; 3 coded batches -as BF4, BF5, BF6, ‘Dashmulkadha’: Manufacturer 3; 3 coded batches as KF, KF8, KF9 were found to contain : 12.8% w/w, 0.294 mg/ml%, 0.429 mg/ ml%, 0.314 mg/ml%, 0.077 mg/ml%, 0.071 mg/ml%, 0.145 mg/ml%, 0.176 mg/ml%, 0.242 mg/ml%, 0.098 mg/ml% of Apigenin and 4.7% w/w, 0.542 mg/ml%, 0.365 mg/ml%, 0.569 mg/ml%, 0.343 mg/ml%, 0.311 mg/ml%, 0.607 mg/ ml%, 0.812 mg/ml%, 0.828 mg/ml%, 0.439 mg/ml% of Luteolin respectively. In stem powder of P. integrifolia 19.84 mg/gm% Apigenin and 7.433 mg/gm% Luteolin was calculated. The estimation shows variance in manufacturers and even within batches, but will be quality control parameter. The method was validated for specificity, linearity, accuracy, precision, and robustness. It was found to be linear in range of 40-120 ng/band with regression coefficient 0.9983, 0.9997 for Apigenin and luteolin. 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引用次数: 0

摘要

Dashmula是阿育吠陀的十根组合,用于治疗肝、肾、子宫的各种疾病。根据世界卫生组织的指导方针,草药的疗效和质量参数的标准化是必要的。因此,通过本研究,我们将采用芹菜素和木犀草素作为活性生物标记物,通过开发和验证的HPTLC技术,对‘Dashmula’,P. integrifolia和选定批次的上市制剂进行标准化,同时进行定量和指纹识别。建立流动相甲苯:乙酸乙酯:甲酸(6:4:0.15),在347 nm等吸收波长下,标准芹菜素和木犀草素的保留系数分别为0.39和0.29。三叶藤乙酸乙酯提取物(PI-ET), ' Dashmularishtha ':制造商1;编号为DF1、DF2、DF3、厂家2的3个批次;3个编号批次-如BF4, BF5, BF6, ' Dashmulkadha ':制造商3;3个编码批次KF、KF8、KF9的芹菜素含量分别为:12.8% w/w、0.294 mg/ml%、0.429 mg/ml%、0.314 mg/ml%、0.077 mg/ml%、0.071 mg/ml%、0.145 mg/ml%、0.176 mg/ml%、0.242 mg/ml%、0.098 mg/ml%; 4.7% w/w、0.542 mg/ml%、0.365 mg/ml%、0.569 mg/ml%、0.343 mg/ml%、0.311 mg/ml%、0.607 mg/ml%、0.812 mg/ml%、0.828 mg/ml%、0.439 mg/ml%。综合叶茎粉中芹菜素19.84 mg/gm%,木犀草素7.433 mg/gm%。该估计在不同的生产厂家,甚至在同一批次内显示差异,但将是质量控制参数。验证了该方法的特异性、线性度、准确度、精密度和鲁棒性。芹菜素和木犀草素在40 ~ 120 ng/波段范围内呈线性关系,回归系数分别为0.9983、0.9997。对芹菜素和木犀草素峰值分别为80,100和120%的提取物PI-ET和DF1进行了百分比回收率研究,对日内和日内精密度进行了单向方差分析,发现F值低于表中F(2,6)值5.14,因此所得值无显著差异。
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Validation and Development of HPTLC Method for Simultaneous Estimation of Apigenin and Luteolin in Selected Marketed Ayurvedic Formulations of âÂÂDashmulaâ and in Ethyl Acetate Extract of Premna integrifolia L.
Dashmula are specific ayurvedic combination of ten roots used for various disorders of liver, kidney, uterus. Standardisation of herbals are necessity for efficacy and quality parameter as per WHO guidelines. Therefore, through this original research attempt was made to standardise one of ‘Dashmula’, P. integrifolia and selected batches of marketed formulation using Apigenin and Luteolin as active biological marker for simultaneous quantification and fingerprinting through developed and validated HPTLC techniques. Developed mobile phase Toluene: Ethyl acetate: Formic acid (6:4:0.15) gave Rf (Retention factor) 0.39 and 0.29 for Standard Apigenin and Luteolin respectively at 347 nm iso absorptive wavelength. The ethyl acetate extract of P. integrifolia (PI-ET), ‘Dashmularishtha’: Manufactuer 1; 3 coded batches as DF1, DF2, DF3, Manufacturer 2; 3 coded batches -as BF4, BF5, BF6, ‘Dashmulkadha’: Manufacturer 3; 3 coded batches as KF, KF8, KF9 were found to contain : 12.8% w/w, 0.294 mg/ml%, 0.429 mg/ ml%, 0.314 mg/ml%, 0.077 mg/ml%, 0.071 mg/ml%, 0.145 mg/ml%, 0.176 mg/ml%, 0.242 mg/ml%, 0.098 mg/ml% of Apigenin and 4.7% w/w, 0.542 mg/ml%, 0.365 mg/ml%, 0.569 mg/ml%, 0.343 mg/ml%, 0.311 mg/ml%, 0.607 mg/ ml%, 0.812 mg/ml%, 0.828 mg/ml%, 0.439 mg/ml% of Luteolin respectively. In stem powder of P. integrifolia 19.84 mg/gm% Apigenin and 7.433 mg/gm% Luteolin was calculated. The estimation shows variance in manufacturers and even within batches, but will be quality control parameter. The method was validated for specificity, linearity, accuracy, precision, and robustness. It was found to be linear in range of 40-120 ng/band with regression coefficient 0.9983, 0.9997 for Apigenin and luteolin. Percentage recovery study carried out for extract PI-ET and DF1 with spike of Apigenin and Luteolin at 80, 100 and 120% level, carried out for inter and intraday precision, subjected for one way ANOVA and found F value is below tabulated F(2,6) value 5.14, therefore there is no significance variance of obtained values.
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