1DZnO 与抗 CYFRA 21-1 的协同组装:光学生物传感的物理化学方法。

IF 5 Q1 ENGINEERING, BIOMEDICAL
BME frontiers Pub Date : 2024-09-18 eCollection Date: 2024-01-01 DOI:10.34133/bmef.0064
Rafael A Salinas, Shirlley E Martínez Tolibia, Patricia G Zayas-Bazán, Sandra E Rodil, Mathew T Mathew, Andrés Navarrete, Guillermo Santana, Ateet Dutt
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引用次数: 0

摘要

目的:我们对一维氧化锌纳米线(1DZnO)进行了全面的物理化学分析,并结合了抗 CYFRA 21-1 固定化技术,以促进高达 10 纳克 ml-1 的快速光学生物标记物检测。影响声明:这项研究通过研究 1DZnO 与这些生物受体的纳米级整合,提供可靠的光致发光输出信号,强调了概念验证 1DZnO 纳米平台在快速检测癌症生物标记物方面的有效性。导言:医疗保健领域对快速准确预后的迫切需求推动了用于癌症检测的灵敏生物传感纳米平台的兴起,而生物标记物的鉴定则使其受益匪浅。CYFRA 21-1 是早期预测癌症形成的可靠靶标,可在血液、唾液和血清中感知。然而,1DZnO 纳米结构还很少应用于 CYFRA 21-1 的检测。方法:我们评估了 1DZnO 与抗 CYFRA 21-1 抗体之间的纳米级相互作用,以开发在两种不同基质中快速检测 CYFRA 21-1:磷酸盐缓冲液(PBS)和人工唾液。利用傅立叶变换红外光谱对化学修饰进行了跟踪,而透射电子显微镜和能量色散光谱则证实了纳米结构上抗原与抗体之间的相互作用。结果:我们的研究结果表明,1DZnO 纳米平台具有很高的抗体固定效率,可在 5 分钟检测时间内对 PBS 和人工唾液中的 CYFRA 21-1 进行快速检测。光致发光测量还显示了不同生物标记物浓度(10 至 1,000 纳克 ml-1)下的不同光学响应。结论5 分钟后获得的可分辨的光致发光信号反应肯定了 1DZnO 纳米平台在光学生物标记物检测方面的进一步发展潜力,可应用于早期癌症预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic Assembly of 1DZnO and Anti-CYFRA 21-1: A Physicochemical Approach to Optical Biosensing.

Objective: We conducted a comprehensive physicochemical analysis of one-dimensional ZnO nanowires (1DZnO), incorporating anti-CYFRA 21-1 immobilization to promote fast optical biomarker detection up to 10 ng ml-1. Impact Statement: This study highlights the effectiveness of proof-of-concept 1DZnO nanoplatforms for rapid cancer biomarker detection by examining the nanoscale integration of 1DZnO with these bioreceptors to deliver reliable photoluminescent output signals. Introduction: The urgent need for swift and accurate prognoses in healthcare settings drives the rise of sensitive biosensing nanoplatforms for cancer detection, which has benefited from biomarker identification. CYFRA 21-1 is a reliable target for the early prediction of cancer formation that can be perceptible in blood, saliva, and serum. However, 1DZnO nanostructures have been barely applied for CYFRA 21-1 detection. Methods: We assessed the nanoscale interaction between 1DZnO and anti-CYFRA 21-1 antibodies to develop rapid CYFRA 21-1 detection in two distinct matrices: PhosphateBuffered Saline (PBS) buffer and artificial saliva. The chemical modifications were tracked utilizing Fourier transform infrared spectroscopy, while transmission electron microscopy and energy dispersive spectroscopy confirmed antigen-antibody interplay over nanostructures. Results: Our results show high antibody immobilization efficiencies, affirming the effectiveness of 1DZnO nanoplatforms for rapid CYFRA 21-1 testing within a 5-min detection window in both PBS and artificial saliva. Photoluminescence measurements also revealed distinct optical responses across biomarker concentrations ranging from 10 to 1,000 ng ml-1. Conclusion: Discernible PL signal responses obtained after 5 min affirm the potential of 1DZnO nanoplatforms for further advancement in optical biomarker detection for application in early cancer prognosis.

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CiteScore
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