Spectrophotometric Method Using the Derivative for the Determination of the Drug Losartan

IF 0.8 4区 化学 Q4 SPECTROSCOPY
Maha A. Mohammed, Kawther Ahmed Sadiq, Elham N. Mezaal, Dheefaf F. Hassan
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Abstract

A sensitive, easy, and low-cost method used in the determination of pure forms of losartan and mebeverine hydrochloride, also in pharmaceutical preparations with derivative spectrometry using UV-Vis technology. This method depends on measuring the first derivative of the spectrum using zero cross, peak to base line, and peak area. The linear range of concentrations used was equal to 2–14 ppm for losartan, whereas for mebeverine hydrochloride it was equal to 2–16 ppm in a mixture. For losartan, in the presence of mebeverine hydrochloride, 12 ppm by utilizing peak to baseline correlation coefficients 0.9984, 0.9994, and peak area 0.9972, whereas for mebeverine hydrochloride in the presence of losartan, 12 ppm by utilizing peak to fundamental correlation coefficients 0.9952, 0.9966, 0.9957, and peak area 0.9970, 0.9971, 0.9968, 0.9971. The limit of detection for each drug, losartan and mebeverine hydrochloride, is equal to 0.0113 ppm. The accuracy and precision of the method were estimated by calculating relative standard deviation (%RSD) values less than 3% while maintaining a recovery percentage of acceptable value. The proposed method proved effective and efficient at estimating both losartan and mebeverine hydrochloride, in the presence of the other in a mixture of the two without interference, despite the closeness of their spectral absorption peaks. There are no other more accurate methods for estimating the two in a mixture than the proposed method. The proposed method is considered one of the most direct and economical methods that do not require reagents or additional materials for conducting reactions and studying the optimal conditions for those interactions. Thus, it is considered one of the green chemistry techniques that reduce the use of chemicals and reagents in the process of estimating these drugs in a mixture and in a shorter period of time. The proposed method can be used to estimate the different properties in a mixture of the two compounds whose absorption spectra are close.

使用衍生物的分光光度法测定药物洛沙坦
一种灵敏、简便、低成本的方法,用于测定药物制剂中的纯品盐酸洛沙坦和美贝维林,也可使用紫外可见技术的衍生光谱法。该方法利用零交叉、峰至基线和峰面积测量光谱的一阶导数。洛沙坦的线性浓度范围为 2-14 ppm,而盐酸甲贝维林在混合物中的线性浓度范围为 2-16 ppm。对于洛沙坦,在有盐酸美贝维林存在的情况下,利用峰与基线的相关系数 0.9984、0.9994 和峰面积 0.9972,可测得 12 ppm;而对于盐酸美贝维林,在有洛沙坦存在的情况下,利用峰与基线的相关系数 0.9952、0.9966、0.9957 和峰面积 0.9970、0.9971、0.9968、0.9971,可测得 12 ppm。洛沙坦和盐酸甲泼尼龙的检出限均为 0.0113 ppm。通过计算相对标准偏差(%RSD)值小于 3%,同时保持回收率为可接受值,估计了该方法的准确度和精密度。事实证明,尽管洛沙坦和盐酸甲贝维林的光谱吸收峰很接近,但在两者的混合物中同时存在另一种药物时,所提出的方法能有效且高效地估算出两者的含量,而不会产生干扰。目前还没有比该方法更准确的方法来估算混合物中的这两种药物。建议的方法被认为是最直接、最经济的方法之一,它不需要试剂或其他材料来进行反应和研究这些相互作用的最佳条件。因此,它被认为是绿色化学技术之一,可在较短时间内减少混合物中这些药物的估算过程中化学品和试剂的使用。所提出的方法可用于估算吸收光谱接近的两种化合物混合物的不同性质。
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来源期刊
CiteScore
1.30
自引率
14.30%
发文量
145
审稿时长
2.5 months
期刊介绍: Journal of Applied Spectroscopy reports on many key applications of spectroscopy in chemistry, physics, metallurgy, and biology. An increasing number of papers focus on the theory of lasers, as well as the tremendous potential for the practical applications of lasers in numerous fields and industries.
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