分光光度法同时测定利伐沙班和氯吡格雷二元混合物中的含量

M. Sharafeldin, F. Ibrahim, S. Shalan, H. Abdelaziz
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引用次数: 3

摘要

建立了三种快速、准确、简便的分光光度法测定RIV和CLP的二元混合物和片剂剂型。方法(1)为一阶导数分光光度法,分别在289和249.5 nm的零交叉波长处测量导数振幅来估计RIV和CLP。RIV和CLP的线性范围分别为2.0 ~ 20.0 μg/ml和5.0 ~ 60.0 μg/ml,检出限分别为0.211和0.361 μ ml,检出限分别为0.641和1.095 μ ml。方法(二)为比值导数分光光度法。每一种药物的比例光谱是通过将其光谱除以另一种药物的恒定浓度作为除数得到的。在相同的线性范围内,RIV和CLP分别在256 nm和214.5 nm处测得导数振幅,LOQ分别为0.137和0.485 μg mL-1, LOQ分别为0.417和1.471 μg mL-1。方法(III)为吸光度比法,记录两种药物在RIV波长λ1(232)等吸收点和λ2 (249) λmax处的吸光度。最终浓度由Q方程得到。该方法与第一种方法在相同的浓度范围内呈线性关系,RIV和CLP的LOQ分别为0.272和0.485 μ mL-1, LOQ分别为0.826和1.471 μ mL-1。根据ICH指南对建议的方法进行了验证。所建立的方法成功地应用于两种药物在实验室制备的复方片剂中的分析。将所得结果与参考方法进行统计比较,结果吻合较好,并证实本文方法与参考方法在准确度和精密度上均无显著差异。
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Spectrophotometric Methods for Simultaneous Determination of Rivaroxaban and Clopidogrel in Their Binary Mixture
Three rapid, accurate and very simple derivative spectrophotometric methods for RIV and CLP assay in their binary mixture and tablet dosage forms were developed. Method (I) is first derivative spectrophotometric method, derivative amplitudes were measured at the zero crossing wavelength of 289 and 249.5 nm for estimation of RIV and CLP, respectively. The linearity is over the range 2.0 - 20.0 μg/ml for RIV and 5.0 - 60.0 μg/ml for CLP with LOD of 0.211 and 0.361 μg mL-1 and LOQ of 0.641 and 1.095 μg mL-1 for RIV and CLP, respectively. Method (II) is ratio derivative spectrophotometric method. The ratio spectra of each drug were derived by dividing its spectra on a constant concentration of the other drug as a divisor. Derivative amplitudes were measured at 256 nm for RIV and at 214.5 nm for CLP over the same linearity range as the first method with LOD of 0.137 and 0.485 μg mL-1 and LOQ of 0.417 and 1.471 μg mL-1 for RIV and CLP, respectively. Method (III) is absorbance ratio method, absorbance of both drugs were recorded at two wavelengths λ1 (232) iso-absorptive point and λ2 (249) λmax of RIV. The final concentrations were obtained by applying the Q equations. The method was linear over the same concentration range as the first method with LOD of 0.272 and 0.485 μg mL-1 and LOQ of 0.826 and 1.471 μg mL-1 for RIV and CLP, respectively. The proposed methods were validated as per ICH guidelines. The proposed methods were successfully applied to both drugs analysis in their laboratory prepared co formulated tablet. Statistical comparison of the obtained results with those of the reference method show good agreement and confirm that there were no significant difference in the accuracy and precision between the proposed and reference one respectively.
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