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Development and validation of a rapid derivative spectrophotometric method for simultaneous determination of acetaminophen, ibuprofen and caffeine

机译:同时测定对乙酰氨基酚,布洛芬和咖啡因的快速导数分光光度法的开发和验证

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A zero-crossing derivative spectrophotometric method was used for the simultaneous determination of acetaminophen, ibuprofen and caffeine. The derivative spectra of standard solutions of each compound were obtained at different orders to find out the suitable zero-crossing points. Under the optimized conditions, determination of acetaminophen was performed at wavelengths of 311 and 270 nm using the third order (Delta lambda = 24.5) and fourth order (Delta lambda = 12.0) derivative spectra, respectively. Ibuprofen and caffeine were determined at wavelengths of 235 and 300 nm using the second order (Delta lambda = 21.0) and fourth order (Delta lambda = 27.0) derivative spectra. The method was found to be linear (r (2) > 0.998) in the range of (mu g/mL) 5-50 for acetaminophen, 5-30 for ibuprofen and 1-7 for caffeine in the presence of other compounds. The within-day and between-day precision and accuracy of the proposed method were acceptable (CV < 3% and error < 2%) for all three components and the proposed method was satisfactory for quality control purposes. The method was successfully applied to the simultaneous determination of acetaminophen, ibuprofen and caffeine in pharmaceutical dosage forms without any interference from excipients and there was no need to any prior separation before analysis.
机译:零交叉导数分光光度法用于同时测定对乙酰氨基酚,布洛芬和咖啡因。以不同的顺序获得每种化合物的标准溶液的导数光谱,以找出合适的过零点。在优化的条件下,分别使用三阶(Δλ= 24.5)和四阶(Δλ= 12.0)导数光谱在311和270 nm波长处进行对乙酰氨基酚的测定。使用二阶(德尔塔λ= 21.0)和四阶(德尔塔λ= 27.0)导数光谱在235和300 nm的波长处测定布洛芬和咖啡因。发现该方法是线性的(r(2)> 0.998),在其他化合物存在下,对乙酰氨基酚的范围为(μg / mL)5-50,对布洛芬为5-30,对咖啡因为1-7。所提方法的日内和日间精度和准确度对于所有三个组件均可接受(CV <3%,误差<2%),并且所提方法对于质量控制而言是令人满意的。该方法已成功应用于药物剂型中对乙酰氨基酚,布洛芬和咖啡因的同时测定,而不受赋形剂的干扰,并且在分析之前无需进行任何事先分离。

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