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首页> 外文期刊>Asian journal of research in chemistry >A Novel Validated Stability Indicating Chromatographic Method for the Simultaneous Estimation of Ascorbic acid and Gallic acid in the Ayurvedic Capsule Dosage form of Amla by UFLC
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A Novel Validated Stability Indicating Chromatographic Method for the Simultaneous Estimation of Ascorbic acid and Gallic acid in the Ayurvedic Capsule Dosage form of Amla by UFLC

机译:用UFLC同时估算Amla的阿育吠陀胶囊剂量形式中的抗坏血酸和没食子酸的新型验证稳定性指示色谱方法

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摘要

An Ultra Fast liquid chromatographic method has been developed and validated for simultaneous estimation of ascorbic and gallic acid in both API and Ayurvedic formulation. Chromatographic separation of compounds was carried out with C8columnby using a mobile phase of methanol: phosphate buffer, PH 3.0 (1: 5) at a flow rate of 1.0 ml/ min. UV detection was performed using PDA detectors at 264 nm. The method was validated for accuracy, precision, linearity, LOD, LOQ and robustness in accordance with ICH guidelines. Amounts of ascorbic and gallic acid detected in capsule were 99.20% and 99.45%. Total run time was below 3 min, ascorbic and gailic acid was eluted with retention times of 1.541 and 2.591 min respectively. Validation revealed that the method is specific, accurate, precise, reliable and reproducible. Calibration plots were linear over the concentration ranges 1-9 μg/ml for ascorbic acid and for gallic acid, respectively. Limits of detection were 0.0382 and 0.14811 μg/ml and limits of quantification were 0.1159 and 0.4488 μg/ml for ascorbic and gallic acid, respectively. Recovery was 99.60 -100.28% and 100.26 -101.35% for ascorbic and gallic acid, respectively. The stress degradation studies were performed for both API and Ayurvedic as per ICH guidelines, the degradation was observed in oxidative, photolytic, hydrolytic degradation under acidic, alkaline conditions and dry heat induced studies. The proposed method is rapid, simple and also it can be applied for the routine analysis of herbal formulations.
机译:已经开发并验证了一种超快速液相色谱方法,可同时估算API和阿育吠陀制剂中的抗坏血酸和没食子酸。使用甲醇:磷酸盐缓冲液,PH 3.0(1:5)的流动相,以1.0 ml / min的流速,用C8色谱柱进行化合物的色谱分离。使用PDA检测器在264 nm处进行UV检测。该方法已按照ICH指南验证了准确性,精密度,线性,LOD,LOQ和鲁棒性。胶囊中检测到的抗坏血酸和没食子酸的量分别为99.20%和99.45%。总运行时间在3分钟以下,洗脱的抗坏血酸和盖利酸的保留时间分别为1.541和2.591分钟。验证表明,该方法具有特异性,准确性,精确性,可靠性和可重复性。校准曲线在抗坏血酸和没食子酸的浓度范围分别为1-9μg/ ml时是线性的。抗坏血酸和没食子酸的检出限分别为0.0382和0.14811μg/ ml,定量限分别为0.1159和0.4488μg/ ml。抗坏血酸和没食子酸的回收率分别为99.60 -100.28%和100.26 -101.35%。根据ICH指南对API和Ayurvedic进行了应力降解研究,在酸性,碱性条件和干热诱导研究中观察到了氧化降解,光降解,水解降解。所提出的方法快速,简便,也可用于草药配方的常规分析。

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