Asma S. Al-Wasidi , Mahmoud A. Mohamed , Hoda A. Ahmed , Manal A. Almalki , Alaa A. Ahmed-Anwar
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MIR and SOL at λmax of 248.9 nm and 229.8 nm have a zero-order (D<sup>0</sup>) after being multiplied by a divisor. The MCR technique has successfully addressed the issue of spectral overlaps for SOL and MIR at 218.5 and 249.7 nm wavelengths. The second method, UPLC densitometry, separates pharmaceuticals using a UPLC C18 1.7 µm (2.1 × 50 mm) column with Ethanol: phosphate buffer pH 4.2 (35:65 v/v) mobile phase at a 0.6 ml/min flow rate, detecting drugs at 210 nm. Calibration curves for both techniques showed a correlation coefficient greater than 0.999 for SOL and MIR in the 1–65 µg mL<sup>−1</sup>, 1–60 µg mL<sup>−1</sup>, and 5–25 µg mL<sup>−1</sup>, respectively. The methods were validated according to International Conference on Harmonization (ICH) principles. 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引用次数: 0
摘要
本研究采用两种直接超高效液相色谱法和分光光度法对广泛用于治疗膀胱过度活动症(OAB)的米拉贝琼(MIR)和索利那新(SOL)进行了分析评估。这些方法是利用 AGREE、GAPI、AGREEprep、ComplexGAPI、AMGS、ESA、HPLC-EAT、AMVI 和 BAGI 工具开发的环保型方法。分光光度法,包括一阶导数比分光光度法(1DD),分别在 224.8 纳米和 258.6 纳米波长处测量 SOL 和 MIR。一种称为扩展比值减法(EXRSM)的方法用于解决 SOL 和 MIR 之间的重叠问题。在这种方法中,二元混合物光谱被除数整除。从高原区减去一个恒定值。在 λmax 为 248.9 nm 和 229.8 nm 处的 MIR 和 SOL 在乘以除数后具有零阶 (D0)。MCR 技术成功地解决了 SOL 和 MIR 在 218.5 和 249.7 nm 波长处的光谱重叠问题。第二种方法是 UPLC 密度测定法,使用 UPLC C18 1.7 µm (2.1 × 50 mm) 色谱柱,以乙醇:pH 值为 4.2 的磷酸盐缓冲液(35:65 v/v)为流动相,流速为 0.6 ml/min,在 210 nm 波长处检测药物,从而分离药物。两种技术的校准曲线显示,SOL 和 MIR 在 1-65 µg mL-1、1-60 µg mL-1 和 5-25 µg mL-1 范围内的相关系数分别大于 0.999。这些方法根据国际协调会议(ICH)的原则进行了验证。这些技术为传统方法提供了经济、环保的替代方法,促进了分析化学的可持续发展。
Comparative analysis using UPLC and UV methods for concurrent quantification of therapeutic drugs for overactive bladder: Effective approach in green and white chemistry
This study evaluates the analysis of Mirabegron (MIR) and Solifenacin (SOL), widely used for treating overactive bladder (OAB), using two direct UPLC and spectrophotometric techniques. These methods were developed to be environmentally friendly, utilizing AGREE, GAPI, AGREEprep, ComplexGAPI, AMGS, ESA, HPLC-EAT, AMVI, and BAGI tools. Spectrophotometry, including the first derivative ratio spectrophotometric method (1DD), measures SOL and MIR at 224.8 nm and 258.6 nm, respectively. A method known as the extended ratio subtraction method (EXRSM) is used to resolve the overlap between the SOL and MIR. In this method, the binary mixture spectrum is divided by the divisor. A constant value is subtracted from the plateau region. MIR and SOL at λmax of 248.9 nm and 229.8 nm have a zero-order (D0) after being multiplied by a divisor. The MCR technique has successfully addressed the issue of spectral overlaps for SOL and MIR at 218.5 and 249.7 nm wavelengths. The second method, UPLC densitometry, separates pharmaceuticals using a UPLC C18 1.7 µm (2.1 × 50 mm) column with Ethanol: phosphate buffer pH 4.2 (35:65 v/v) mobile phase at a 0.6 ml/min flow rate, detecting drugs at 210 nm. Calibration curves for both techniques showed a correlation coefficient greater than 0.999 for SOL and MIR in the 1–65 µg mL−1, 1–60 µg mL−1, and 5–25 µg mL−1, respectively. The methods were validated according to International Conference on Harmonization (ICH) principles. These techniques offer cost-effective, eco-friendly alternatives to traditional methods, promoting sustainability in analytical chemistry.