肌萎缩侧索硬化
免疫分析
化学
医学
内科学
抗体
免疫学
疾病
作者
Xuan Luo,Amir Heydari,Danielle Renfrey,Zoe Gardner,Shan He,Youhong Tang,Gregory A. Weiss,Mary‐Louise Rogers,Colin L. Raston
出处
期刊:Chemsuschem
[Wiley]
日期:2024-07-11
卷期号:17 (21)
被引量:2
标识
DOI:10.1002/cssc.202401008
摘要
Abstract Healthcare facilities produce millions of tons of waste annually, with a significant portion consisting of diagnostic plasticware. Here, we introduce a new detection platform that completely replaces traditional assay plates with a piece of membrane, offering a much greener and more sustainable alternative. The membrane, integrated within the portable vortex fluidic device (P‐VFD), enables rapid detection of a clinically relevant protein biomarker, urinary p75 ECD . This biomarker is utilized to evaluate the prognosis, disease severity, and progression of amyotrophic lateral sclerosis (ALS). This assay has a limit‐of‐detection (LOD) of 4.03 pg, which is comparable to the plate‐based assay (2.24 pg) and has been optimised through a full factorial design of experiments (DOE) and response surface methodology (RSM). P‐VFD has great potential in quantifying p75 ECD in human biofluids and can significantly reduce the assay time to 5 min compared to the current plate‐based p75 ECD ELISA assay (3 days), with at least a 4.4‐fold reduction in the usage of the detection antibody.
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