Department of Pharmaceutical Analysis, College of Pharmacy, Third Military Medical University, Chongqing, 400038, China.
Center for Clinical Trial, Xinqiao Hospital, Third Military Medical University, Chongqing, 400038, China.
Anal Biochem. 2019 Jan 1;564-565:64-71. doi: 10.1016/j.ab.2018.10.011. Epub 2018 Oct 9.
Circulating tumor cells (CTCs) from peripheral blood of cancer patients are considered as one of the most promising pharmacodynamic (PD) biomarkers due to its non-invasive property in disease diagnosis and prognosis. However, the detection of extremely low number of CTCs in patient blood requires methods with high sensitivity and accuracy. We fabricated an arrayed geometrically enhanced mixing (GEM) chip with a "dislocation herringbone" layout based on cell immunoaffinity. By optimizing the injection and rinsing flow rate, an average cell capture rate of 87.02% and an average capture purity of 99.58% were achieved using the human lung adenocarcinoma cell lines H1975. In addition, we determined the specificity, precision, accuracy, and detection limit of our chip. The results demonstrated the chip was stable, accurate and reliable for the "liquid biopsy" of lung cancer cells using the peripheral blood of patients. Our chip can also be used to evaluate the potency of different drugs against tumor cells in parallel due to the presence of four independent microchannels.
循环肿瘤细胞(CTCs)来源于癌症患者外周血,因其在疾病诊断和预后方面具有非侵入性而被认为是最有前途的药效动力学(PD)生物标志物之一。然而,要检测患者血液中极其少量的 CTCs,需要使用具有高灵敏度和准确性的方法。我们基于细胞免疫亲和力,制造了一种具有“位错人字形”布局的阵列几何增强混合(GEM)芯片。通过优化注射和冲洗流速,使用人肺腺癌细胞系 H1975 实现了平均 87.02%的细胞捕获率和平均 99.58%的捕获纯度。此外,我们还确定了我们芯片的特异性、精密度、准确性和检测限。结果表明,该芯片在使用患者外周血进行肺癌细胞的“液体活检”方面稳定、准确、可靠。由于存在四个独立的微通道,我们的芯片还可用于平行评估不同药物对肿瘤细胞的药效。