用于皮质醇定量的激光诱导石墨烯基法布里-佩罗腔无标记免疫传感器

IF 6.5 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Sensors and Actuators Reports Pub Date : 2024-01-19 DOI:10.1016/j.snr.2024.100186
Hugo Coutinho Gomes , Xuecheng Liu , António Fernandes , Catarina Moreirinha , Ragini Singh , Santosh Kumar , Florinda Costa , Nuno Santos , Carlos Marques
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引用次数: 0

摘要

人类和动物体内的压力生物标志物是健康的一个关键指标,为了对压力生物标志物进行实时健康评估,对压力生物标志物进行监测的需求日益强烈。为此,我们报告了一种基于激光诱导石墨烯(LIG)的光纤免疫传感器,可用于皮质醇激素的潜在定量和监测。所开发的传感器是利用法布里-佩罗空腔原理制造的。空腔中填充了聚酰亚胺(PI),在某些情况下,PI 中还混合了金纳米颗粒。对干涉仪进行了温度和折射率测试,发现由于加入了金纳米粒子,对折射率的灵敏度提高了两倍。此外,使用 20 kHz CO2 脉冲激光将 PI 腔部分转化为 LIG。由此产生的 LIG 形貌多孔,呈现出叶状纹理。LIG 的存在在干涉仪内形成了第二个空腔,因此干涉仪的光谱响应类似于 Vernier 效应。LIG 改良型干涉仪的折射率特性表明,由于 LIG 腔的产生,其灵敏度提高了 15.3 倍。然后,用抗皮质醇对干涉仪进行功能化,以提高其对皮质醇的亲和力。在几毫微克/毫升的浓度范围内(0.5 至 3 毫微克/毫升),灵敏度高达 -34.7 ± 0.7 nm/log(毫微克/毫升)。结果表明,与其他皮质醇传感器相比,灵敏度最多提高了 50 倍。拟议传感器的检测限为 0.1 纳克/毫升。研究还表明,传感器的响应不受葡萄糖、蔗糖、果糖和抗坏血酸等物质的干扰。这项研究为新型皮质醇生物传感器奠定了基础,它以简单、高灵敏度的方式展示了巨大的检测潜力,为实际样品中的相关生物医学和环境监测应用开辟了道路。作为未来的纲要,将利用合成和真实样品,完成在存在干扰物的情况下检测皮质醇的选择性研究,以充分研究这些传感工具在现实生活中的潜力。
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Laser-Induced graphene-based Fabry-Pérot cavity label-free immunosensors for the quantification of cortisol

There is a strong and growing need to monitor stress biomarkers in human beings and animals for real-time wellness assessment, which is a key indicator of health. Toward this, we report an optical fiber immunosensor based on laser-induced graphene (LIG) for the potential quantification and monitoring of cortisol hormone. The developed sensors were created using the Fabry-Pérot cavity principle. The cavities were filled with polyimide (PI) and, in some cases, PI mixed with gold nanoparticles. The interferometers were tested for temperature and refractive index, and an increase of two times in the sensitivity to the refractive index was observed due to the addition of the gold nanoparticles. In addition, the PI cavity was partially transformed into LIG using a CO2 20 kHz pulsed laser. The resulting LIG morphology was quite porous and presented a leafy texture. The presence of LIG creates a second cavity within the interferometer, and as a consequence, the spectral response of the interferometers resembled the Vernier effect. The refractive index behavior of the LIG-modified interferometers shows improvements in sensitivity up to 15.3 times due to the creation of the LIG cavity. The interferometers were then functionalized with anti-cortisol to promote an affinity for cortisol. Excellent sensitivities of up to -34.7 ± 0.7 nm/log(ng/mL) were achieved within few ng/mL concentration ranges (within the 0.5 to 3 ng/mL). The results obtained show an increase of up to 50 times in sensitivity when compared with other cortisol sensors. The achieved limit of detection was 0.1 ng/mL for the proposed sensors. The sensors’ responses were also shown to be immune to the interference from substances such as glucose, sucrose, fructose, and ascorbic acid. This study lays the foundation for new cortisol biosensors demonstrating a great potential for detection in a simple and highly sensitive way, opening its path for relevant biomedical and environmental monitoring applications in real samples. As a future outline, selectivity studies employing the detection of cortisol in the presence of interfering agents, both using synthetic and real samples, will be accomplished in order to fully investigate the potential of these sensing tools in real-life scenarios.

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期刊介绍: Sensors and Actuators Reports is a peer-reviewed open access journal launched out from the Sensors and Actuators journal family. Sensors and Actuators Reports is dedicated to publishing new and original works in the field of all type of sensors and actuators, including bio-, chemical-, physical-, and nano- sensors and actuators, which demonstrates significant progress beyond the current state of the art. The journal regularly publishes original research papers, reviews, and short communications. For research papers and short communications, the journal aims to publish the new and original work supported by experimental results and as such purely theoretical works are not accepted.
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