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Quantification of theophylline or paracetamol in milk matrices by high-performance liquid chromatography

机译:高效液相色谱法定量测定牛奶基质中的茶碱或扑热息痛

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摘要

A simple, accurate and sensitive high-performance liquid chromatography (HPLC) method was developed, validated and applied to the determination of either theophylline or paracetamol in milk-based samples. The method allowed drug quantification in fresh and powdered milk with a relatively short run time of analysis and it was also successfully applied to the quantification of the drugs in solid dosage forms intended for pediatric use. Moreover, the main significant advantages over other published works are the simplicity of the sample preparation, reduced assay time and sample loss. The method meets the International Conference on Harmonization guideline for analytical methods validation regarding specificity, linearity, accuracy, precision, specificity and robustness as required by health authorities and applied by industry while designing and marketing new drug products. The technique encompasses the separation of the analytes with a reverse phase C18 column under isocratic conditions and UV detection at 272 nm and 243 nm, respectively, for theophylline and paracetamol. The lower limit of quantification for both drugs was determined as 0.2 µg/mL and the between-batch accuracy was approximately 99.7%. This HPLC method allows quantification of theophylline and paracetamol in milk matrices and it can be applied in the design, development and production of milk-based pediatric dosage forms.
机译:建立了一种简单,准确,灵敏的高效液相色谱(HPLC)方法,并将其验证并用于乳基样品中茶碱或扑热息痛的测定。该方法可以在较短的分析时间内对新鲜奶粉和奶粉中的药物进行定量,并且还成功地应用于了用于儿科的固体剂型中的药物定量。此外,与其他已发表的作品相比,主要的显着优点是样品制备的简便性,减少的测定时间和样品损失。该方法符合国际协调会议指南的要求,有关分析方法的验证涉及卫生当局的要求,并且在设计和销售新药品时,行业会应用有关特异性,线性,准确性,精密度,特异性和耐用性的分析方法。该技术包括在等度条件下使用反相C18色谱柱分离分析物,并在272 nm和243 nm处分别对茶碱和对乙酰氨基酚进行UV检测。两种药物的定量下限均为0.2 µg / mL,批间准确度约为99.7%。这种HPLC方法可以对牛奶基质中的茶碱和扑热息痛进行定量,可用于设计,开发和生产基于牛奶的儿科剂型。

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