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一步法无设备细胞外囊泡浓缩法,使用超吸收聚合物珠。

Single-step equipment-free extracellular vesicle concentration using super absorbent polymer beads.

机构信息

Department of Bioengineering and Nano-Bioengineering Incheon National University Incheon Republic of Korea.

Center for Scientific Instrumentation Korea Basic Science Institute Chungbuk Republic of Korea.

出版信息

J Extracell Vesicles. 2021 Feb;10(4):e12074. doi: 10.1002/jev2.12074. Epub 2021 Feb 23.

Abstract

Extracellular vesicles (EVs) contain useful biomarkers for disease diagnosis and are promising biomaterials for the delivery of therapeutic molecules . Accordingly, an efficient concentration method is necessary for large-scale production or high-throughput isolation of EVs from bulk liquid samples, including culture medium and body fluids, to achieve their clinical application. However, current EV concentration methods, including ultrafiltration, are limited with respect to cost, efficiency, and centrifugation time. In this study, we developed the first single-step, equipment-free EV concentration method using super absorbent polymer (SAP) beads. SAP beads absorb small molecules, including water, via nano-sized channels but expel and thereby concentrate EVs. Consequently, the beads drastically enrich EVs by reducing the solution volume in a single step, without affecting EV characteristics. Moreover, the purity of the concentrated EV solution was high due to the absorption of protein impurities by SAP beads. To further demonstrate the versatility of the method, we showed that SAP beads successfully enrich EVs in human urine samples and culture medium, enabling better isolation performance than conventional ultrafiltration. We believe the newly developed approach and insight gained in this study will facilitate the use of EVs as prominent biomaterials for disease diagnosis and therapy.

摘要

细胞外囊泡(EVs)包含用于疾病诊断的有用生物标志物,并且是治疗分子递药的有前途的生物材料。因此,需要有效的浓缩方法,以便从包括培养基和体液在内的大量液体样品中大规模生产或高通量分离 EVs,从而实现其临床应用。然而,目前的 EV 浓缩方法(包括超滤)在成本、效率和离心时间方面都受到限制。在这项研究中,我们开发了使用超吸水性聚合物 (SAP) 珠的首个单步、无设备的 EV 浓缩方法。SAP 珠通过纳米通道吸收包括水在内的小分子,但通过排出从而浓缩 EVs。因此,珠粒通过在单个步骤中减少溶液体积,急剧富集 EVs,而不会影响 EV 的特性。此外,由于 SAP 珠吸收了蛋白质杂质,因此浓缩的 EV 溶液的纯度很高。为了进一步证明该方法的多功能性,我们表明 SAP 珠粒可成功富集人尿液样品和培养基中的 EVs,其分离性能优于传统的超滤。我们相信,新开发的方法和本研究中获得的见解将促进 EVs 作为用于疾病诊断和治疗的重要生物材料的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/feb4/7902527/53e63889dc3d/JEV2-10-e12074-g001.jpg

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