首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >SIMULTANEOUS ESTIMATION OF CURCUMINOIDS, PIPERINE, AND GALLIC ACID IN AN AYURVEDIC FORMULATION BY VALIDATED HIGH-PERFORMANCE THIN LAYER CHROMATOGRAPHIC METHOD
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SIMULTANEOUS ESTIMATION OF CURCUMINOIDS, PIPERINE, AND GALLIC ACID IN AN AYURVEDIC FORMULATION BY VALIDATED HIGH-PERFORMANCE THIN LAYER CHROMATOGRAPHIC METHOD

机译:经验证的高效薄层色谱法同时估算阿育吠陀制剂中的姜黄素,哌啶和没食子酸

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Objective: The present study was proposed to quantitatively estimate the amount of three marker compounds; curcuminoids, piperine, and gallic acid in a multicomponent ayurvedic formulation using high-performance thin layer chromatographic (HPTLC) method for routine analytical work. Methods: TLC separation was performed on silica gel 60 F plates using toluene:ethyl acetate:formic acid:methanol (5.6:2.2:1.2:1.0 v/v/v/v) as mobile phase. Plate was developed by to a distance of 90 mm at ambient room temperature with 20 minutes saturation time. Densitometric analysis was performed at 327 nm. Method was validated as per International Conference on Harmonization Q2 (R1) guideline also. 254 Results: Piperine, curcuminoids, and gallic acid were separated on TLC at retention factor values of 0.71, 0.61, and 0.29, respectively. The described method was linear over the range of 300-700 ng/spot, 100-300 ng/spot, and 250-550 ng/spot, respectively, for curcuminoids, piperine, and gallic acid. The accuracy of the method was assessed by recovery studies and was found to be 101.71%, 99.67%, and 99.59% for curcuminoids, piperine, and gallic acid, respectively. The amount of curcuminoids, piperine, and gallic acid in the ayurvedic formulation was found to be 3.99% w/w, 1.9% w/w, and 0.8% w/w, respectively, when analyzed quantitatively by developed validated HPTLC method. Conclusion: The method can be used as a tool for quality control of herbal formulation.
机译:目的:本研究旨在定量估计三种标记物的含量。使用高效薄层色谱(HPTLC)方法进行常规分析的多组分阿育吠陀制剂中的姜黄素,胡椒碱和没食子酸。方法:在硅胶60 F板上,以甲苯:乙酸乙酯:甲酸:甲醇(5.6:2.2:1.2:1.0 v / v / v / v)作为流动相进行TLC分离。在室温下,以20分钟的饱和时间将板显影至90mm的距离。在327nm下进行光密度分析。该方法也根据国际协调大会第二季度(R1)指南进行了验证。 254结果:薄层色谱中的胡椒碱,姜黄素和没食子酸的保留因子分别为0.71、0.61和0.29。对于姜黄素,胡椒碱和没食子酸,所描述的方法分别在300-700 ng / spot,100-300 ng / spot和250-550 ng / spot范围内是线性的。通过回收率研究评估了该方法的准确性,发现姜黄素,胡椒碱和没食子酸的准确度分别为101.71%,99.67%和99.59%。用发达的经过验证的HPTLC方法进行定量分析时,印度草药制剂中的姜黄素,胡椒碱和没食子酸的量分别为3.99%w / w,1.9%w / w和0.8%w / w。结论:该方法可作为中草药制剂质量控制的工具。

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