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首页> 外文期刊>Chromatographia >Quantitative HPLC Determination and Stability Studies of Pyridostemin in Extracts and Water Dispersible Granule Formulations of Stemona curtisii
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Quantitative HPLC Determination and Stability Studies of Pyridostemin in Extracts and Water Dispersible Granule Formulations of Stemona curtisii

机译:蛇麻风提取物和水分散性颗粒剂制剂中吡啶硫醇的定量HPLC测定和稳定性研究

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A reversed-phase high-performance liquid chromatographic method has been developed and validated for the determination of pyridostemin, the major pesticidal alkaloid found in Stemona curtisii. This methodology was applied to the investigation of plant extracts and water dispersible granule formulations. Stability indicating procedures have also been carried out. The chromatographic separation was on a C18 column with a mixture of acetonitrile–water–triethylamine (30:70:0.12, v/v/v), using UV detection at 300 nm. Validation procedures showed that the method was specific, accurate and precise. The response was linear over a range of 5–25 μg mL−1 with recoveries in the range of 98.28–102.85%. The RSD for intra- and inter-day precision were <0.72 and <1.29%, respectively. Extraction of plant material with dichloromethane gave a significantly higher pyridostemin content in the crude extracts when compared with extractions in methanol. Partial purification of the crude extracts by silica gel column chromatography was used to concentrate the mixture about fourfold. Degradation behavior of pyridostemin in the partially purified extracts followed first-order kinetics. The main pathways for its decomposition were base hydrolysis and oxidation.
机译:已经开发了一种反相高效液相色谱方法,并已用于测定蛇麻风中主要的杀虫生物碱吡啶酮的测定。该方法学被用于植物提取物和水分散性颗粒制剂的研究。稳定性指示程序也已执行。色谱分离是在C 18 色谱柱上进行的,使用的是乙腈-水-三乙胺的混合物(30:70:0.12,v / v / v),使用300 nm的紫外检测。验证程序表明该方法具有特异性,准确性和准确性。响应在5–25μgmL -1 范围内呈线性,回收率在98.28–102.85%之间。日内和日间精度的RSD分别为<0.72%和<1.29%。与在甲醇中提取相比,用二氯甲烷提取植物材料时,粗提取物中的吡啶氨基甜菊素含量明显更高。通过硅胶柱色谱法部分纯化粗提取物,将混合物浓缩约四倍。部分纯化的提取物中嘧啶类固醇的降解行为遵循一级动力学。其分解的主要途径是碱水解和氧化。

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