Collection of serum albumin aggregate nanoparticles from human plasma by dielectrophoresis

Author:

Ware Jason12ORCID,Shea Delaney12ORCID,Lim Jeong Youn3ORCID,Malakian Anna1ORCID,Armstrong Randall1ORCID,Pethig Ronald4ORCID,Ibsen Stuart12ORCID

Affiliation:

1. Cancer Early Detection Advanced Research Center, Knight Cancer Institute Oregon Health and Science University Portland Oregon USA

2. Department of Biomedical Engineering, School of Medicine Oregon Health and Science University Portland Oregon USA

3. Biostatistics Shared Resource, Knight Cancer Institute Oregon Health and Science University Portland Oregon USA

4. Institute for Integrated Micro and Nano Systems School of Engineering & Electronics The University of Edinburgh Edinburgh UK

Abstract

AbstractDielectrophoresis (DEP) is a fast and reliable nanoparticle recovery method that utilizes nonuniform electric fields to manipulate particles based on their material composition and size, enabling recovery of biologically‐derived nanoparticles from plasma for diagnostic applications. When applying DEP to undiluted human plasma, collection of endogenous albumin proteins was observed at electric field gradients much lower than predicted by theory to collect molecular proteins. To understand this collection, nanoparticle tracking analysis of bovine serum albumin (BSA) dissolved in 0.5× phosphate‐buffered saline was performed and showed that albumin spontaneously formed aggregate nanoparticles with a mean diameter of 237 nm. These aggregates experienced a dielectrophoretic force as a function of aggregate radius rather than the diameter of individual protein molecules which contributed to their collection. In high conductance buffer (6.8 mS/cm), DEP was able to move these aggregates into regions of high electric field gradient, and in lower conductance buffer (0.68 mS/cm), these aggregates could be moved into high or low gradient regions depending on the applied frequency. Disruption of BSA aggregates using a nonionic detergent significantly decreased the particle diameter, resulting in decreased dielectrophoretic collection of albumin which increased the collection consistency of particles of interest. These results provide techniques to manipulate albumin aggregates via DEP, which impacts collection of diagnostic biomarkers.

Funder

National Institutes of Health

Publisher

Wiley

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