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Holographic particle characterization treats holographic microscopy of colloidal particles as an inverse problem whose solution yields the diameter, refractive index and three-dimensional position of each particle in the field of view, all with exquisite precision. This rich source of information on the composition and dynamics of colloidal dispersions has created new opportunities for fundamental research in soft-matter physics, statistical physics and physical chemistry, and has been adopted for product development, quality assurance and process control in industrial applications. Aberrations introduced by real-world imaging conditions, however, can degrade performance by causing systematic and correlated errors in the estimated parameters. We identify a previously overlooked source of spherical aberration as a significant source of these errors. Modeling aberration-induced distortions with an operator-based formalism identifies a spatially varying phase factor that approximately compensates for spherical aberration in recorded holograms. Measurements on model colloidal dispersions demonstrate that phase-only aberration compensation greatly improves the accuracy of holographic particle characterization without significantly affecting measurement speed for high-throughput applications. 

Holographic particle characterization yields the diameter of individual colloidal spheres with nanometer precision and can resolve probe beads growing as molecules bind to their surfaces. We demonstrate label-free holographic assays for antibodies and for antigenic proteins from pathogenic viruses, including SARS-CoV-2 and H1N1. 

The size of a probe bead reported by holographic particle characterization depends on the proportion of the surface area covered by bound target molecules and so can be used as an assay for molecular binding. We validate this technique by measuring the kinetics of irreversible binding for the antibodies immunoglobulin G (IgG) and immunoglobulin M (IgM) as they attach to micrometer-diameter colloidal beads coated with protein A. These measurements yield the antibodies’ binding rates and can be inverted to obtain the concentration of antibodies in solution. Holographic molecular binding assays therefore can be used to perform fast quantitative immunoassays that are complementary to conventional serological tests.