Specialized greenness sustainability tools for evaluation of the spectrophotometric methodologies greenness: Spectral signal manipulation for resolving the interfering telmisartan and metoprolol succinate spectra in their bulk and pharmaceutical formulation

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS Analytical biochemistry Pub Date : 2024-11-08 DOI:10.1016/j.ab.2024.115711
Michael Gamal Fawzy , Soad S. Abd El-Hay , Alaa Ahmed Mostafa , Youstina Mekhail Metias
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Abstract

Hypertension is a leading cause of cardiovascular mortality, often accompanied by complications such as arrhythmia and stroke. This silent killer requires a multifaceted pharmacological approach for effective management. This article presents new, environmentally friendly spectrophotometric methods for simultaneous quantification of telmisartan (TER) and metoprolol succinate (MTR) in laboratory prepared mixtures and pharmaceutical formulations. The suggested methodologies include the following: area under the curve method (AUC) utilizing area at specific wavelength ranges 228–233 nm (λ1λ2) and 240–245 nm (λ3λ4) for each analyte and Fourier self-deconvolution method (FD) depending on built-in function to address spectral interferences. In addition, the induced dual wavelength method (IDWL) employing equality factors to obtain absorbance differences at designated wavelengths, ratio difference method (RD) utilizing divisor-based ratio spectra where the utilized divisors were TER 40 μg/mL and MTR 90 μg/mL, and ratio derivative method (RDV) generating spectra through first derivative application that was measured at 266 nm and 246 nm for TER and MTR, respectively. These methods offer green alternatives for the accurate and precise determination of TER and MTR with exceptional linearity of 3–45, and 15–200 μg/mL for TER and MTR, respectively. Furthermore, the methods showed a coefficient of determination exceeding 0.9995 and good detection and quantification levels. A comprehensive greenness assessment, employing five distinct evaluation tools, confirmed the reduced environmental impact of the proposed methods in terms of waste generation, chemical consumption, and instrument safety. Successful analysis of pharmaceutical formulations and laboratory prepared mixtures containing different TER and MTR ratios confirmed the validity of the proposed methods. Standard addition studies further supported these findings, and the statistical results were comparable to those obtained using a reference method.

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评估分光光度法绿色可持续性的专用工具:光谱信号操作,用于消除替米沙坦和琥珀酸美托洛尔散装和药物制剂中的干扰光谱。
高血压是心血管疾病死亡的主要原因,通常伴有心律失常和中风等并发症。要有效控制这一无声杀手,需要采取多方面的药物治疗方法。本文介绍了一种新型、环保的分光光度法,用于同时定量检测实验室制备的混合物和药物制剂中的替米沙坦(TER)和琥珀酸美托洛尔(MTR)。建议采用的方法包括:利用特定波长范围 228-233 nm (λ1 - λ2) 和 240-245 nm (λ3 - λ4) 下的面积对每种分析物进行曲线下面积法 (AUC),以及傅立叶自旋法 (FD),根据内置功能解决光谱干扰问题。此外,诱导双波长法 (IDWL) 利用相等因子获得指定波长的吸光度差值;比值差法 (RD) 利用基于除数的比值光谱,其中使用的除数为 TER 40 μg/mL 和 MTR 90 μg/mL;比值导数法 (RDV) 通过一阶导数应用生成光谱,分别在 266 nm 和 246 nm 处测量 TER 和 MTR。这些方法为准确和精确地测定 TER 和 MTR 提供了绿色的替代方法,TER 和 MTR 的线性范围分别为 3-45 和 15-200 μg/mL。此外,这些方法的测定系数超过 0.9995,检测和定量水平良好。利用五种不同的评估工具进行的综合绿色评估证实,所建议的方法在废物产生、化学品消耗和仪器安全方面减少了对环境的影响。对含有不同 TER 和 MTR 比率的药物制剂和实验室制备的混合物的成功分析证实了建议方法的有效性。标准添加研究进一步支持了这些发现,统计结果与使用参考方法获得的结果相当。
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来源期刊
Analytical biochemistry
Analytical biochemistry 生物-分析化学
CiteScore
5.70
自引率
0.00%
发文量
283
审稿时长
44 days
期刊介绍: The journal''s title Analytical Biochemistry: Methods in the Biological Sciences declares its broad scope: methods for the basic biological sciences that include biochemistry, molecular genetics, cell biology, proteomics, immunology, bioinformatics and wherever the frontiers of research take the field. The emphasis is on methods from the strictly analytical to the more preparative that would include novel approaches to protein purification as well as improvements in cell and organ culture. The actual techniques are equally inclusive ranging from aptamers to zymology. The journal has been particularly active in: -Analytical techniques for biological molecules- Aptamer selection and utilization- Biosensors- Chromatography- Cloning, sequencing and mutagenesis- Electrochemical methods- Electrophoresis- Enzyme characterization methods- Immunological approaches- Mass spectrometry of proteins and nucleic acids- Metabolomics- Nano level techniques- Optical spectroscopy in all its forms. The journal is reluctant to include most drug and strictly clinical studies as there are more suitable publication platforms for these types of papers.
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