对咖啡因增刊分析的导数分析方法的开发和验证

Dzurriatul Maghfiroh, Eva Monica, M. Afthoni
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引用次数: 0

摘要

补充剂是为了满足身体健康需要而食用的健康产品。它通常呈片剂或粉末状,含有有效成分,如咖啡因。2004年,POM发布了第2号法令。HK.00.05.23.3644关于“食品补充剂监管的基本规定”该决定指出,每日咖啡因摄入量的最大限制是150毫克/天,超过150毫克/天的摄入量可能会产生副作用。在本研究中,我们进行了一项实验研究来验证和发展紫外可见分光光度法的分析方法,并利用导数法分析补充剂中的咖啡因。本研究对四类溶剂进行了优化,选择甲醇作为柠檬酸混合物的溶剂,由于分析中存在波长偏移,采用dA/d的导数法,最大波长为239 nm。用选择性、线性度、精密度和准确度等参数验证了该方法的有效性。在宣布有效性后,对补充剂中的咖啡因含量进行了测定。用紫外-可见分光光度法测定咖啡因,其测定系数(R2)为0.988;相关系数(r) 0.976, p值为5,46 × 10^-5;检出限4.5 ppm;定量限13.6 ppm;偏差度为3.750%,准确率为97.443%。结果表明,该方法是有效的。该方法可用于咖啡因分析。
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PENGEMBANGAN DAN VALIDASI METODE SPEKTROFOTOMETRI UV VIS METODE DERIVATIF UNTUK ANALISIS KAFEIN DALAM SUPLEMEN
Supplements are health products that are consumed to meet the body's health needs. Usually shaped in dosage tablets or powder forms, it contains active ingredients, such as caffeine. In 2004, POM issued a decree of No. HK.00.05.23.3644 concerning 'Basic Provisions for Supervision of Food Supplements.' This decision states that the maximum limit of daily caffeine intake is 150 mg/day, and more than 150 mg/day consumption could cause side effects. In this study, an experimental study was conducted to validate and develop the analysis of the method using UV-Vis spectrophotometry using the derivative method to analyze the caffeine in supplements. In this research, optimization of solvent from four categories has been done, and methanol was selected as the solvent with the mixture of citric acid, and then carried out using a derivative method with dA/d by using a maximum wavelength of 239 nm because in this analysis there was a wavelength shift. The parameters for selectivity, linearity, precision, and accuracy were utilized to prove the validity of the method. After the validity was declared, the determination of caffeine content in the supplement was performed. The result from caffeine analysis with spectrophotometry UV-Vis with derivatives method show a result of coefficient of determination (R2) 0.988; coefficient of correlation (r) 0.976 with pvalue 5,46 x 10^-5; limit of detection 4,5ppm; limit of quantification 13,6ppm; and degree of deviation 3.750% with an accuracy of 97.443%. These results conclude that the method was valid. This method can be used for caffeine analysis.
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