在流体动力封闭分离系统中使用多样品进样,通过 CZE 对治疗肽进行定量分析。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Ondrej Stefanik, Peter Mikus, Juraj Piestansky
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引用次数: 0

摘要

在现代医学中,治疗肽已成为一类创新且前景广阔的治疗化合物。合成肽类似物曲普瑞林(triptorelin)和兰瑞奥肽(lanreotide)以其显著的临床通用性和有效性而闻名。在本研究中,我们介绍了基于在流体动力封闭系统(HCS)中进行的毛细管区带电泳、紫外检测和重复进样的新型方法的开发和验证。据我们所知,我们开发出了第一种基于毛细管电泳的兰瑞奥肽测定方法,同时也是第一种测定曲普瑞林的水力封闭系统方法。采用50 mM甲酸为背景电解质,添加0.05%(v/v)甲基羟乙基纤维素,实现了最高的分离效率和信号强度。所提出的方法具有良好的性能特点,即校准曲线(r2 超过 0.99)、低检出限(在水基质中为 0.25 微克/毫升,在合成尿液中为 0.5 微克/毫升)、可接受的精密度(日内重复性的相对标准偏差在 2.2% 至 9.6% 之间,日间重现性在 5.2% 至 14.9% 之间)和准确度(相对误差在 91.1% 至 107.8% 之间)。随后,采用该方法对市售药物剂型(注射用粉末)和添加剂合成尿样中的曲普瑞林进行了定量检测。此外,还根据新的蓝色适用性等级指数对所开发的方法进行了评估,结果表明这些方法具有极佳的适用性。这些结果共同表明了所建议的方法在质量控制和临床研究方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative analysis of therapeutic peptides by CZE using multiple sample injection in hydrodynamically closed separation system.

Therapeutic peptides have emerged as an innovative and promising class of therapeutic compounds in modern medicine. Synthetic peptide analogs triptorelin and lanreotide are known for their pronounced clinical versatility and potency. In this study, we present the development and validation of novel methods based on capillary zone electrophoresis performed in hydrodynamically closed system (HCS) and paired with ultraviolet detection and repeated injection sample introduction. To the best of our knowledge, we developed the first capillary electrophoresis-based method for the determination of lanreotide, and concurrently, the first HCS method for the determination of triptorelin. Maximal separation efficiency and signal intensity were achieved using background electrolytes composed of 50 mM formic acid with the addition of 0.05% (v/v) methyl-hydroxyethyl cellulose. The proposed methods exhibit favorable performance characteristics, namely, calibration curve (r2 exceeding 0.99), low limits of detection (0.25 µg/mL in a water matrix and 0.5 µg/mL in synthetic urine), acceptable precision (relative standard deviation ranging from 2.2% to 9.6% for intraday repeatability and between 5.2% and 14.9% for interday reproducibility), and accuracy (relative errors falling within the 91.1%-107.8% range). The method for triptorelin determination was then used for its quantification in a commercially available drug dosage form (powder for injection) and in spiked synthetic urine samples. The developed methods were also evaluated according to the novel blue applicability grade index, revealing their superior applicability. The results collectively point out the potential of the proposed methods for both quality control and clinical investigations.

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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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