High-gradient microstructured hybrid microfluidic chip for rare tumor cell capture

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS Analytical and Bioanalytical Chemistry Pub Date : 2025-03-14 DOI:10.1007/s00216-025-05825-z
Wen Ding, Wu Ye, Huayan Liu, Jianbo Yang, Chengxing Chu, Huancheng Zhu, Jiakang Wang, Luping Zhou, Ming Zhao, Ming Liu
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Abstract

Cancer remains the leading cause of death worldwide, and early detection can significantly reduce patient mortality. Circulating tumor cells (CTCs), which are tumor cells shed from the primary tumor and transported to distant sites through the bloodstream, are key biomarkers for cancer diagnosis and contain critical information reflecting the primary tumor, making them important for monitoring cancer progression. Microfluidic chips utilizing a purely physical capture technique based on the size and deformability differences between CTCs and other blood cells have proven to be effective in capturing CTCs. This study investigates three high-gradient microstructured hybrid microfluidic chips (HGMH-Chips), each incorporating a microarray structure and a distinct geometric gradient design: linear, sawtooth, and waveform. Multiphysics simulations revealed significant differences in pressure distribution among the chip configurations. Notably, the sawtooth design exhibited a more uniform pressure drop, with only 25% of the particles in the high-pressure region. We employed two cancer cell lines (MDA-MB-231 and A549) to evaluate the chip’s capture capability. Additionally, we compared the capture efficiency and cell viability across the three designs in a single cancer cell system. Experimental results demonstrated that the sawtooth chip achieved a capture efficiency of up to 70%. When applied to mixed samples containing leukocytes, the high-gradient design exhibited a capture purity of up to 98%, effectively isolating a small number of cancer cells from complex samples. This model holds promise for the capture of CTCs in complex systems. Furthermore, the microarray structure aids in stabilizing the captured cancer cells, enhancing separation efficiency. This study presents a novel chip structure design for tumor cell capture, which holds promise for improving the capture of tumor cells in complex biological samples.

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用于捕获罕见肿瘤细胞的高梯度微结构混合微流控芯片。
癌症仍然是全球死亡的主要原因,而早期检测可以大大降低患者的死亡率。循环肿瘤细胞(CTCs)是从原发肿瘤脱落并通过血液运输到远处的肿瘤细胞,是诊断癌症的关键生物标记物,包含反映原发肿瘤的关键信息,因此对监测癌症进展非常重要。事实证明,基于 CTC 与其他血细胞之间的大小和变形性差异,利用纯物理捕获技术的微流控芯片能有效捕获 CTC。本研究调查了三种高梯度微结构混合微流控芯片(HGMH-Chips),每种芯片都结合了微阵列结构和独特的几何梯度设计:线性、锯齿和波形。多物理场模拟显示,不同芯片配置的压力分布存在显著差异。值得注意的是,锯齿形设计的压降更均匀,只有 25% 的颗粒处于高压区。我们采用了两种癌细胞系(MDA-MB-231 和 A549)来评估芯片的捕获能力。此外,我们还比较了三种设计在单一癌细胞系统中的捕获效率和细胞存活率。实验结果表明,锯齿形芯片的捕获效率高达 70%。当应用于含有白细胞的混合样本时,高梯度设计的捕获纯度高达 98%,能有效地从复杂样本中分离出少量癌细胞。这种模式有望在复杂系统中捕获 CTC。此外,芯片结构有助于稳定捕获的癌细胞,提高分离效率。本研究提出了一种用于捕获肿瘤细胞的新型芯片结构设计,有望改善复杂生物样本中肿瘤细胞的捕获。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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