Rapid Separation and Analysis of Exosomes in Milk Sample by on-Line Nano-Liquid Chromatography.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
ELECTROPHORESIS Pub Date : 2025-05-21 DOI:10.1002/elps.8155
Cemil Aydoğan, Zeynep Günyel, Sarah Alharthi, Hakiye Aslan, İbrahim Y Erdoğan, Ziad El Rassi
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Abstract

Exosomes are very small vesicles of 30-150 nm average particle size and hold great potential in new therapeutic applications. The aim of this study is to develop a new method for the isolation and analysis of exosomes in milk via hydrophobic interaction chromatography (HIC), including salting-out process in nano-liquid chromatography (nano-LC). On the basis of this approach, a trap column combined with graphene oxide (GO)-based monolithic nano-column was used for on-line analysis of exosomes in nano-LC. The monolith was prepared by an in situ polymerization of butyl methacrylate (BMA), ethylene glycol dimethacrylate (EDMA), and methacryloyl graphene oxide nanoparticles (MGONPs). The final solution was introduced into a fused silica capillary with a 50 µm i.d. for polymerization. After preparation, the column was further modified with dimethyloctadecylchlorosilane (DODCS) to increase its hydrophobicity. The characterization of monolith was performed using scanning electron microscopy (SEM) and chromatographic examination. The final monolith was applied for the isolation and analysis of exosomes in milk via HIC-nano-LC. Nanoparticle tracking analysis (NTA), SEM, and Fourier transform-infrared (FT-IR) for the tandem characterization of milk exosomes were used, whereas step gradient elution was employed for HIC. The results demonstrated good ability to isolate exosomes from milk with three dilution factors, and a loading capacity of 7.3 ± 02 × 1011 exosomes could be obtained using the on-line nano-LC system. The developed method holds many advantages and may be adapted for the isolation of exosomes from a diverse range of media.

在线纳米液相色谱法快速分离和分析牛奶样品中的外泌体。
外泌体是一种平均粒径为30- 150nm的小囊泡,在新的治疗应用中具有很大的潜力。本研究的目的是建立一种利用疏水相互作用色谱(HIC)分离和分析牛奶中外泌体的新方法,包括纳米液相色谱(nano-LC)中的盐析工艺。在此基础上,利用基于氧化石墨烯(GO)的单片纳米柱结合陷阱柱对纳米lc中外泌体进行在线分析。采用原位聚合法制备了甲基丙烯酸丁酯(BMA)、乙二醇二甲基丙烯酸酯(EDMA)和甲基丙烯酰氧化石墨烯纳米颗粒(MGONPs)。将最终溶液引入直径为50µm的熔融石英毛细管中进行聚合。制备完成后,用二甲基十八烷基氯硅烷(DODCS)对柱进行进一步修饰,以提高其疏水性。采用扫描电镜(SEM)和色谱法对其进行表征。最后的整体应用于HIC-nano-LC分离和分析牛奶中的外泌体。采用纳米颗粒跟踪分析(NTA)、扫描电镜(SEM)和傅里叶变换红外(FT-IR)对乳外泌体进行串联表征,而HIC采用阶梯梯度洗脱。结果表明,在三种稀释倍数下,乳中外泌体的分离效果良好,在线纳米- lc系统可获得7.3±02 × 1011个外泌体。所开发的方法具有许多优点,可适用于从各种培养基中分离外泌体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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