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用于在体温下检测癌症核酸生物标志物的集成装置。

Integrated Device for Cancer Nucleic Acid Biomarker Detection at Body Temperature.

作者信息

Chen Chang, Wu Bin, Li Xuesong, Jin Yuhang, Zhang Hangyu, Liu Bo, Zhang Zhengyao, Li Na

机构信息

Central Hospital of Dalian University of Technology, Dalian 116033, China.

Faculty of Medicine, Dalian University of Technology, Dalian 116024, China.

出版信息

Micromachines (Basel). 2025 Feb 7;16(2):192. doi: 10.3390/mi16020192.

Abstract

The quantitative analysis of nucleic acid markers is extensively utilized in cancer detection. However, it faces significant challenges, such as the need for specialized detection devices and the inherent complexity of testing procedures. To address these issues, this study proposes a simplified, rapid, and user-friendly platform for cancer nucleic acid marker detection. We firstly designed a polydimethylsiloxane (PDMS) device for the isothermal amplification reaction of nucleic acid biomarkers based on reverse-transcription recombinase-aided amplification (RT-RAA) technology. Specifically, three potential cancer nucleic acid biomarkers, carcinoembryonic antigen (CEA), prostate-specific antigen (PSA), and prostate cancer antigen 3 (PCA3) were amplified from human serum or urine samples in the PDMS device at body temperature. The reaction chamber was directly integrated with nucleic acid test strips labeled with colloidal gold nanoparticles, allowing for the visual observation of the detection results for the amplification products. The optimal reaction conditions, such as pH, reaction time, antibody, and streptavidin concentration, were defined after a series of optimization studies. The findings demonstrated that the optimal RT-RAA reaction time was 20 min, the primary antibodies were labeled with colloidal gold to the greatest extent at pH 8.5, and the optimal concentrations of secondary antibody and streptavidin were 1.0 mg/mL and 0.5 mg/mL, respectively. Furthermore, this novel detection approach could not only exhibit excellent sensitivity and specificity but also show high accuracy for the analysis of nucleic acid biomarkers in both clinical serum and urine samples. Therefore, the simplified and more convenient operation platform provides a new insight for the semi-quantitative analysis of cancer nucleic acid biomarkers and the rapid screening of early cancer, thereby offering a promising alternative to oncological point-of-care testing (POCT) diagnostics.

摘要

核酸标志物的定量分析在癌症检测中得到了广泛应用。然而,它面临着重大挑战,例如需要专门的检测设备以及检测程序本身的复杂性。为了解决这些问题,本研究提出了一种用于癌症核酸标志物检测的简化、快速且用户友好的平台。我们首先基于逆转录重组酶辅助扩增(RT-RAA)技术设计了一种用于核酸生物标志物等温扩增反应的聚二甲基硅氧烷(PDMS)装置。具体而言,在体温下,从人血清或尿液样本中在PDMS装置中扩增三种潜在的癌症核酸生物标志物,即癌胚抗原(CEA)、前列腺特异性抗原(PSA)和前列腺癌抗原3(PCA3)。反应室直接与标记有胶体金纳米颗粒的核酸试纸条集成,从而可以直观地观察扩增产物的检测结果。经过一系列优化研究后,确定了最佳反应条件,如pH值、反应时间、抗体和链霉亲和素浓度。研究结果表明,最佳RT-RAA反应时间为20分钟,在pH 8.5时一抗被胶体金标记的程度最大,二抗和链霉亲和素的最佳浓度分别为1.0 mg/mL和0.5 mg/mL。此外,这种新型检测方法不仅具有出色的灵敏度和特异性,而且在临床血清和尿液样本中对核酸生物标志物的分析也显示出高准确性。因此,这个简化且操作更便捷的平台为癌症核酸生物标志物的半定量分析和早期癌症的快速筛查提供了新的思路,从而为肿瘤即时检测(POCT)诊断提供了一种有前景的替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dabb/11857440/c64126db5a9b/micromachines-16-00192-g001.jpg

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