2021
DOI: 10.1002/anie.202108714
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Sink/Float Magnetic Immunoassays for In‐Field Bioassays

Abstract: Analytical tests/devices that are used outside laboratory settings are required to have a very simple analytical protocol to get clearance by regulatory authorities. This study describes sink/float magnetic immunoassays, a new type of rapid, mix‐and‐observe, instrument‐free tests for the detection of biomarkers in untreated biological samples that are very simple and might meet the simple‐to‐use criterion of authorities to be used in the field. These tests can tell whether an analyte is above or below a predet… Show more

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Cited by 5 publications
(3 citation statements)
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“…We employed immunoassay as a format to illustrate the principle of the SOS platform, including sandwich/competitive immunoassays, differential sedimentation of spheres with diverse sizes in solution, and Coulter-principle-based analysis of spheres. The PS 1000μm spheres have a high density and abundant surface binding sites, enabling them to sediment and rapidly participate in the reactions . Meanwhile, the PS μm spheres are uniformly dispersed in solution, which increases their collision and separation probability with PS 1000μm spheres.…”
Section: Resultsmentioning
confidence: 99%
See 2 more Smart Citations
“…We employed immunoassay as a format to illustrate the principle of the SOS platform, including sandwich/competitive immunoassays, differential sedimentation of spheres with diverse sizes in solution, and Coulter-principle-based analysis of spheres. The PS 1000μm spheres have a high density and abundant surface binding sites, enabling them to sediment and rapidly participate in the reactions . Meanwhile, the PS μm spheres are uniformly dispersed in solution, which increases their collision and separation probability with PS 1000μm spheres.…”
Section: Resultsmentioning
confidence: 99%
“…The PS 1000μm spheres have a high density and abundant surface binding sites, enabling them to sediment and rapidly participate in the reactions. 31 Meanwhile, the PS μm spheres are uniformly dispersed in solution, which increases their collision and separation probability with PS 1000μm spheres. The presence of targets induces the formation of sandwich complexes, while the addition of NaOH disrupts the antigen−antibody conjugates and releases the PS μm spheres.…”
Section: Resultsmentioning
confidence: 99%
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