TY - JOUR
T1 - Sustainability-Driven Accelerated Shear-Mediated Immunoassay for Amyotrophic Lateral Sclerosis Detection
AU - Luo, Xuan
AU - Heydari, Amir
AU - Renfrey, Danielle
AU - Gardner, Zoe
AU - He, Shan
AU - Tang, Youhong
AU - Weiss , Gregory
AU - Rogers, Mary-Louise
AU - Raston, Colin
PY - 2024/11/11
Y1 - 2024/11/11
N2 - 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.
AB - 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.
KW - Portable Vortex Fluidic Device
KW - P-VFD
KW - immunoassay
KW - biomarker
KW - ALS
UR - http://www.scopus.com/inward/record.url?scp=85202829403&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/DP200101106
UR - http://purl.org/au-research/grants/ARC/IC190100034
U2 - 10.1002/cssc.202401008
DO - 10.1002/cssc.202401008
M3 - Article
SN - 1864-5631
VL - 17
JO - ChemSusChem
JF - ChemSusChem
IS - 21
M1 - e202401008
ER -