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在质量源于设计驱动的研究中利用绿色色谱法同时分析基本的单片复方抗糖尿病药物组合

Leveraging Green Chromatography in Quality-by-Design-Driven Study for the Simultaneous Analysis of Essential Single-Pill Antidiabetic Drug Combinations.

作者信息

Ibrahim Adel Ehab, Alamir Samy G, Maged Khaled, Magdy Galal, Salman Baher I, Al-Harrasi Ahmed

机构信息

Natural and Medical Sciences Research Center, University of Nizwa, Nizwa City, Oman.

Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Port-Said University, Port-Said, Egypt.

出版信息

J Sep Sci. 2024 Dec;47(24):e70063. doi: 10.1002/jssc.70063.

Abstract

Micellar liquid chromatography (MLC) has proven beneficial efficiency and ecological impact for routine quality control activities. In the proposed study, cyrene was investigated for the first time, together with other green additives, as a novel safe organic solvent in reversed-phase MLC. Quality-by-design (QbD) approach screened their effect on the separation performance. Six antidiabetic drugs from different classes, namely, metformin (MTF), empagliflozin (EMP), ertugliflozin (ERT), linagliptin (LNT), sitagliptin (SIT), and gliclazide (GCZ) were utilized to assess some newly approved antidiabetic drugs and combinations. An organic solvent-free mobile phase consisting of (0.01 M Brij-35, 0.09 M sodium dodecyl sulfate, and 0.01 M ammonium acetate, pH 5.0) separated the studied drugs using an RP-C18 core-shell column. The flow rate was set at 1.2 mL/min, and analytes were detected using a photodiode array detector at 245, 270, and 225 nm. System suitability parameters demonstrated MLC capability to eliminate organic solvents without compromising separation efficiency. The method was validated across a concentration range of 2.0-30.0 µg/mL for EMP, ERT, and LNT, 20.0-120.0 µg/mL for GCZ and SIT, and 100.0-600.0 µg/mL for MTF. The method successfully determined analytes in different single and multicomponent tablets. Greenness assessment was performed using MoGAPI and AGREE metrics.

摘要

胶束液相色谱法(MLC)已被证明在常规质量控制活动中具有良好的效率和生态影响。在本研究中,首次将环戊酮与其他绿色添加剂一起作为反相MLC中的新型安全有机溶剂进行研究。质量源于设计(QbD)方法筛选了它们对分离性能的影响。使用六种不同类别的抗糖尿病药物,即二甲双胍(MTF)、恩格列净(EMP)、依鲁格列净(ERT)、利格列汀(LNT)、西他列汀(SIT)和格列齐特(GCZ)来评估一些新批准的抗糖尿病药物及其组合。由(0.01 M 月桂醇聚醚-35、0.09 M 十二烷基硫酸钠和 0.01 M 醋酸铵,pH 5.0)组成的无有机溶剂流动相使用 RP-C18 核壳柱分离所研究的药物。流速设定为 1.2 mL/min,使用光电二极管阵列检测器在 245、270 和 225 nm 处检测分析物。系统适用性参数表明 MLC 有能力在不影响分离效率的情况下消除有机溶剂。该方法在 2.0 - 30.0 μg/mL 浓度范围内对 EMP、ERT 和 LNT,20.0 - 120.0 μg/mL 对 GCZ 和 SIT,以及 100.0 - 600.0 μg/mL 对 MTF 进行了验证。该方法成功测定了不同单组分和多组分片剂中的分析物。使用 MoGAPI 和 AGREE 指标进行了绿色度评估。

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