首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Optimization and validation of liquid chromatography and headspace-gas chromatography based methods for the quantitative determination of capsaicinoids, salicylic acid, glycol monosalicylate, methyl salicylate, ethyl salicylate, camphor and l-menthol in a topical formulation
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Optimization and validation of liquid chromatography and headspace-gas chromatography based methods for the quantitative determination of capsaicinoids, salicylic acid, glycol monosalicylate, methyl salicylate, ethyl salicylate, camphor and l-menthol in a topical formulation

机译:基于液相色谱和顶空气相色谱的局部制剂中辣椒素,水杨酸,单水杨酸乙二醇酯,水杨酸甲酯,水杨酸乙酯,樟脑和1-薄荷醇的定量方法的优化和验证

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摘要

Capsaicinoids, salicylic acid, methyl and ethyl salicylate, glycol monosalicylate, camphor and l-menthol are widely used in topical formulations to relieve local pain. For each separate compound or simple mixtures, quantitative analysis methods are reported. However, for a mixture containing all above mentioned active compounds, no assay methods were found. Due to the differing physicochemical characteristics, two methods were developed and optimized simultaneously. The non-volatile capsaicinoids, salicylic acid and glycol monosalicylate were analyzed with liquid chromatography following liquid-liquid extraction, whereas the volatile compounds were analyzed with static headspace-gas chromatography. For the latter method, liquid paraffin was selected as compatible dilution solvent. The optimized methods were validated in terms of specificity, linearity, accuracy and precision in a range of 80% to 120% of the expected concentrations. For both methods, peaks were well separated without interference of other compounds. Linear relationships were demonstrated with R 2 values higher than 0.996 for all compounds. Accuracy was assessed by performing replicate recovery experiments with spiked blank samples. Mean recovery values were all between 98% and 102%. Precision was checked at three levels: system repeatability, method precision and intermediate precision. Both methods were found to be acceptably precise at all three levels. Finally, the method was successfully applied to the analysis of some real samples (cutaneous sticks).
机译:辣椒素,水杨酸,水杨酸甲酯和乙酯,单水杨酸乙二醇酯,樟脑和薄荷脑被广泛用于局部制剂中以减轻局部疼痛。对于每种单独的化合物或简单混合物,报告了定量分析方法。然而,对于包含所有上述活性化合物的混合物,未发现测定方法。由于不同的理化特性,同时开发和优化了两种方法。液-液萃取后,用液相色谱法分析非挥发性辣椒素,水杨酸和单水杨酸乙二醇酯,而使用静态顶空-气相色谱法分析挥发性化合物。对于后一种方法,选择液体石蜡作为兼容的稀释溶剂。在预期浓度的80%至120%范围内,针对特异性,线性,准确性和精密度对优化方法进行了验证。对于这两种方法,峰都可以很好地分离,而不会受到其他化合物的干扰。所有化合物的R 2值均高于0.996,表现出线性关系。通过对加标空白样品进行重复回收实验来评估准确性。平均回收率均在98%至102%之间。从三个级别检查精度:系统重复性,方法精度和中间精度。发现这两种方法在所有三个级别上都是可接受的精确度。最终,该方法成功地应用于一些真实样品(皮肤棒)的分析。

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