School of Advanced Technology, Xi'an Jiaotong - Liverpool University, 215123, Suzhou, China; Department of Electrical Engineering and Electronics, University of Liverpool, L69 7ZX, Liverpool, UK; State Key Laboratory for Manufacturing Systems Engineering, Xi'an Jiaotong University, 710049, Xi'an, China.
School of Advanced Technology, Xi'an Jiaotong - Liverpool University, 215123, Suzhou, China.
Anal Chim Acta. 2024 May 1;1301:342447. doi: 10.1016/j.aca.2024.342447. Epub 2024 Mar 4.
Alzheimer's disease (AD), one of the most prevalent neurodegenerative diseases, results in severe cognitive decline and irreversible memory loss. Early detection of AD is significant to patients for personalized intervention since effective cure and treatment methods for AD are still lacking. Despite the severity of the disease, existing highly sensitive AD detection methods, including neuroimaging and brain deposit-positive lesion tests, are not suitable for screening purposes due to their high cost and complicated operation. Therefore, these methods are unsuitable for early detection, especially in low-resource settings. Although regular paper-based microfluidics are cost-efficient for AD detection, they are restricted by a poor limit of detection (LOD).
To address the above limitations, we report the ultrasensitive and low-cost nanocellulose paper (nanopaper)-based analytical microfluidic devices (NanoPADs) for detecting one of the promising AD blood biomarkers (glial fibrillary acidic protein, GFAP) using Surface-enhanced Raman scattering (SERS) immunoassay. Nanopaper offers advantages as a SERS substrate, such as an ultrasmooth surface, high optical transparency, and tunable chemical properties. We detected the target GFAP in artificial serum, achieving a LOD of 150 fg mL.
The developed NanoPADs are distinguished by their cost-efficiency and ease of implementation, presenting a promising avenue for effective early detection of AD's GFAP biomarker with ultrahigh sensitivity. More importantly, our work provides the experimental routes for SERS-based immunoassay of biomarkers on NanoPADs for various diseases in the future.
阿尔茨海默病(AD)是最常见的神经退行性疾病之一,会导致严重的认知能力下降和不可逆转的记忆丧失。早期发现 AD 对患者进行个性化干预非常重要,因为目前仍缺乏有效的 AD 治疗方法。尽管疾病严重,但现有的高灵敏度 AD 检测方法,包括神经影像学和脑沉积阳性病变测试,由于成本高和操作复杂,不适合用于筛查目的。因此,这些方法不适合早期检测,尤其是在资源匮乏的环境中。虽然常规纸质微流控技术在 AD 检测方面具有成本效益,但由于检测限(LOD)较差而受到限制。
为了解决上述限制,我们报告了基于纳米纤维素纸(纳米纸)的超灵敏和低成本分析微流控装置(NanoPAD),用于使用表面增强拉曼散射(SERS)免疫分析检测 AD 的一种有前途的血液生物标志物(胶质纤维酸性蛋白,GFAP)。纳米纸作为 SERS 基底具有许多优势,如超光滑表面、高透光率和可调节的化学性质。我们在人工血清中检测到了目标 GFAP,检测限达到 150 fg mL。
开发的 NanoPAD 具有成本效益和易于实施的特点,为有效早期检测 AD 的 GFAP 生物标志物提供了超灵敏的途径。更重要的是,我们的工作为未来在 NanoPAD 上基于 SERS 的生物标志物免疫分析提供了实验途径,适用于各种疾病。