Sergio Fernández-Trujillo , Gregorio Castañeda-Peñalvo , Juana Rodríguez-Flores , Rosa del Carmen Rodríguez Martín-Doimeadios
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Here, a rapid capillary electrophoresis with diode-array detector methodology was developed and applied for the first time to detect, identify and determine revumenib in complex clinical matrices such as human blood serum in less than 5 min of analysis with a minimal sample preparation procedure based on a protein precipitation with acetonitrile. Various chemical and instrumental critical parameters were rigorously optimized for the separation process in a fused-silica capillary with a background electrolyte of phosphate buffer (50 mM, pH = 2.0) in deionized water. Adequate analytical performance parameters were obtained involving a good linearity, detection and quantification limits at ng mL<sup>−1</sup> levels, and a correct precision and accuracy. Furthermore, this approach can be characterized as an ecofriendly strategy in the bioanalysis field based on an estimated greenness evaluation via AGREEprep and AGREE metrics tool with acceptable scores. 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引用次数: 0
摘要
Revumenib(原SNDX-5613)是一种新型、有效的口服menin抑制剂,用于临床治疗危重患者的急性髓系白血病。然而,安全性仍然是一个值得关注的问题,因为这种抗癌药物的最佳给药时间和剂量。治疗性药物监测是解决药物剂量方案的有效工具。从这个意义上说,需要简单、敏感和准确的生物分析策略。本研究开发了一种快速毛细管电泳二极管阵列检测器方法,并首次应用于检测、鉴定和测定复杂临床基质(如人血清)中的revumenib,分析时间不到5分钟,采用基于乙腈蛋白沉淀的最小样品制备程序。在去离子水中,以磷酸盐缓冲液(50 mM, pH = 2.0)为背景电解质,对熔融石英毛细管分离过程的各种化学和仪器关键参数进行了严格优化。获得了足够的分析性能参数,包括良好的线性,检测和定量限在ng mL−1水平,以及正确的精密度和准确度。此外,这种方法可以被描述为生物分析领域的一种生态友好策略,该策略基于通过AGREEprep和AGREE指标工具进行的可接受分数的估计绿色评估。考虑到这些结果,本工作可以作为一种新的医学工具,成功地应用于常规临床实验室对revumenib的治疗监测,但也可以在未来(预)临床试验和/或阶段做出适当的决定。
A rapid and green analytical strategy to determine menin inhibitor revumenib in human blood serum via CE-DAD
Revumenib (formerly SNDX-5613) is a novel, potent and oral menin inhibitor employed in clinical settings because of treating acute myeloid leukemia in critically ill patients. Nevertheless, safety is still a matter of concern due to the optimal timing of administration and doses of this anticancer agent. An effective tool that allows to solve the drug dosage regimen is therapeutic drug monitoring. In that sense, simple, sensitive and accurate bioanalytical strategies are required. Here, a rapid capillary electrophoresis with diode-array detector methodology was developed and applied for the first time to detect, identify and determine revumenib in complex clinical matrices such as human blood serum in less than 5 min of analysis with a minimal sample preparation procedure based on a protein precipitation with acetonitrile. Various chemical and instrumental critical parameters were rigorously optimized for the separation process in a fused-silica capillary with a background electrolyte of phosphate buffer (50 mM, pH = 2.0) in deionized water. Adequate analytical performance parameters were obtained involving a good linearity, detection and quantification limits at ng mL−1 levels, and a correct precision and accuracy. Furthermore, this approach can be characterized as an ecofriendly strategy in the bioanalysis field based on an estimated greenness evaluation via AGREEprep and AGREE metrics tool with acceptable scores. Considering the results, the present work can be used as a new medical tool and successfully applied in the therapeutic monitoring of revumenib in routine clinical laboratories but also to take appropriate decisions in future (pre)clinical trials and/or phases.
期刊介绍:
The Microchemical Journal is a peer reviewed journal devoted to all aspects and phases of analytical chemistry and chemical analysis. The Microchemical Journal publishes articles which are at the forefront of modern analytical chemistry and cover innovations in the techniques to the finest possible limits. This includes fundamental aspects, instrumentation, new developments, innovative and novel methods and applications including environmental and clinical field.
Traditional classical analytical methods such as spectrophotometry and titrimetry as well as established instrumentation methods such as flame and graphite furnace atomic absorption spectrometry, gas chromatography, and modified glassy or carbon electrode electrochemical methods will be considered, provided they show significant improvements and novelty compared to the established methods.