Enhancing Doxorubicin Detection: Multiphase Electroextraction for Efficient and Affordable UHPLC-DAD Analysis in Saliva.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Denise V M Sousa, Fabiano V Pereira, Ricardo M Orlando
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Abstract

Attesting optimal drug concentrations in biological fluids is crucial to ensure precise dosage adjustment, to guarantee therapy adherence, and to manage side effects in chemotherapy. Accurate drug determination relies on liquid chromatography and advanced detectors, with sample preparation playing a pivotal role, especially in complex matrices such as biological fluids. This study introduces a multiphase electroextraction (MPEE) of doxorubicin (DOX) in saliva by utilizing a paper point, followed by ultra-high-performance liquid chromatography coupled to diode array detection. The extraction time and electric potential were carried out by using the Doehlert optimization approach, whereas the desorption solvent was fine-tuned through the centroid-simplex experimental design. After optimization, DOX and the internal standard were extracted in 35 min, utilizing an applied voltage of 300 V and a multiwell plate capable of simultaneous extraction of 66 samples. The recovery was 87%-101%, with a linear range between 50 and 500 µg L-1 (R2 > 0.999). The intra- and inter-assay coefficients of variation for precision were <10%, and the limit of detection and limit of quantification were 25 and 50 µg L-¹, respectively. When applied to five different fortified saliva samples, there were no statistically significant differences in the detected concentrations. Although the enrichment factor (0.6) was not as high as expected, the other results confirm that the method obtained is suitable for monitoring DOX in this complex matrix and can contribute to further developments in sample preparation using MPEE approaches.

加强多柔比星检测:多相电萃取用于唾液中高效、经济的超高效液相色谱-DAD 分析
检测生物液体中的最佳药物浓度对于确保精确调整剂量、保证治疗的依从性以及控制化疗副作用至关重要。药物的精确测定有赖于液相色谱法和先进的检测器,其中样品制备起着关键作用,尤其是在生物液体等复杂基质中。本研究采用纸点多相电萃取法(MPEE)萃取唾液中的多柔比星(DOX),然后采用超高效液相色谱法和二极管阵列检测器进行检测。萃取时间和电位采用 Doehlert 优化方法,解吸溶剂则通过中心-复数实验设计进行微调。经过优化后,利用 300 V 的外加电压和可同时萃取 66 个样品的多孔板,在 35 分钟内萃取了 DOX 和内标物。回收率为 87%-101%,线性范围在 50 至 500 µg L-1 之间(R2 > 0.999)。精密度的测定内变异系数和测定间变异系数分别为-¹。在对五种不同的强化唾液样本进行检测时,检测到的浓度没有明显的统计学差异。虽然富集因子(0.6)没有预期的那么高,但其他结果证实了所获得的方法适用于监测这种复杂基质中的 DOX,并有助于使用 MPEE 方法制备样品的进一步发展。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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