Silica-coated magnetic nanobeads in a flow enrichment target capture Halbach (FETCH) magnetic separation system for circulating tumor cell enrichment

IF 3 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology FEBS Letters Pub Date : 2025-01-01 DOI:10.1002/1873-3468.15094
Peng Liu, Sitian He, Anouk Mentink, Pieter Hart, Yongjun Wu, Leon W. M. M. Terstappen, Pascal Jonkheijm, Michiel Stevens
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Abstract

Detecting circulating tumor cells (CTCs) is challenging due to their low presence and heterogeneity. Traditional methods using EpCAM-based separation struggle with CTCs that have undergone epithelial-mesenchymal transition, as this results in lower EpCAM expression. This study presents the use of silica-coated magnetic nanobeads functionalized with streptavidin for CTC capture. Using the FETCH magnetic separation system, we validated the capture efficiency of our beads on tumor cells with varying EpCAM expression. Our beads showed superior capture rates for LNCaP (97%), PC3-9 (91%), PC3 (23%), A549 (22%), and T24 (8%) cells compared to commercial MojoSort™ beads. Despite slightly higher nonspecific binding than CellSearch, our beads demonstrated improved sensitivity for EpCAMlow cells, suggesting they have promise for enhanced CTC capture.

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流动富集靶捕获Halbach (FETCH)磁分离系统中二氧化硅包被的磁性纳米珠用于循环肿瘤细胞富集。
检测循环肿瘤细胞(ctc)是具有挑战性的,因为他们的低存在和异质性。使用基于EpCAM的传统分离方法与经历上皮-间质转化的ctc存在冲突,因为这导致EpCAM表达降低。本研究提出了利用链霉亲和素功能化的二氧化硅涂层磁性纳米球捕获CTC。使用FETCH磁分离系统,我们验证了我们的珠粒在不同EpCAM表达的肿瘤细胞上的捕获效率。与商业MojoSort™珠粒相比,我们的珠粒对LNCaP(97%)、PC3-9(91%)、PC3(23%)、A549(22%)和T24(8%)细胞的捕获率更高。尽管比CellSearch的非特异性结合略高,但我们的微珠对EpCAMlow细胞的敏感性有所提高,这表明它们有望增强CTC的捕获。
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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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