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快速毛细管电泳法同时测定药物制剂中阿贝西利、瑞博西利和哌柏西利的含量:一种绿色方法。

Rapid Capillary Electrophoresis Method for Simultaneous Determination of Abemaciclib, Ribociclib, and Palbociclib in Pharmaceutical Dosage Forms: A Green Approach.

机构信息

Department of Pharmaceutical Analysis, Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10000 Zagreb, Croatia.

出版信息

Molecules. 2022 Nov 6;27(21):7603. doi: 10.3390/molecules27217603.

Abstract

Advances in the treatment of HR+/HER2- breast cancer phenotype have been made with the introduction of abemaciclib, ribociclib, and palbociclib, inhibitors of cyclin D dependent kinases 4 and 6 (CDK4/6). Here, a novel, fast, cheap, and green CE method for the simultaneous determination of these three CDK4/6 inhibitors in less than 4 min is proposed for the first time. Separation was achieved by capillary zone electrophoresis in an acidic medium, in accordance with the structures of the analytes and their pKa values. The optimal pH of the running buffer was found to be 2.9. The optimal method conditions were 27.5 kV separation voltage, 30 °C, 5 s injection time under 50 mbar pressure, and 50 mM phosphate background buffer with benzimidazole as an internal standard. The developed method was validated with respect to robustness, selectivity, accuracy, precision, linearity, and limits of detection. The method was shown to be linear in the range of 10 to 100 µg mL with correlation coefficients higher than 0.9981. A greenness assessment of the proposed method was performed, and the method was shown to be green. The validated method was successfully applied to pharmaceutical dosage forms of all CDK4/6 inhibitors.

摘要

CDK4/6 抑制剂的治疗 HR+/HER2- 乳腺癌的研究进展,得益于阿贝西利、瑞博西利和哌柏西利的问世,这三种药物均为细胞周期蛋白依赖性激酶 4 和 6(CDK4/6)抑制剂。本研究首次提出了一种新颖、快速、廉价、绿色的毛细管电泳(CE)方法,可在不到 4 分钟的时间内同时测定这三种 CDK4/6 抑制剂。根据分析物的结构及其 pKa 值,在酸性介质中采用毛细管区带电泳进行分离。运行缓冲液的最佳 pH 值为 2.9。最佳方法条件为 27.5 kV 分离电压、30°C、5 s 进样时间(50 mbar 压力下)和 50 mM 磷酸盐背景缓冲液,以苯并咪唑为内标。该方法经过稳健性、选择性、准确性、精密度、线性和检测限验证。结果表明,该方法在 10 至 100 µg mL 范围内呈线性,相关系数均高于 0.9981。对所提议的方法进行了绿色度评估,结果表明该方法具有绿色性。该验证后的方法成功应用于所有 CDK4/6 抑制剂的药物制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ebb/9657767/d30e5744998a/molecules-27-07603-g001.jpg

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