Buffer pH-Driven Electrokinetic Concentration of Proteins in a Straight Microfluidic Channel

We present a buffer-pH-modulated electrokinetic concentration strategy in MEMS microchannels that harnesses simple pH shifts to neutralize and charge proteins, reversibly “pausing” them at a planar electric-gate electrode by tuning to their isoelectric point (pI) and mobilizing them with slight pH offsets under an applied field. This synergistic coupling of dynamic pH control and electrode-gated focusing, which requires only buffer composition changes, enables rapid and tunable protein capture and release across diverse channel geometries for lab-on-chip, preparative, and point-of-care diagnostics. Moreover, it dovetails with established MEMS biomedical platforms ranging from diagnostics to drug delivery and microsurgery to gene and cell-manipulation devices. Future work on tailored electrode coatings and optimized channel profiles will further boost selectivity, speed, and integration in sub-100 µm MEMS devices.

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Publication Details

Journal
Surfaces
Published
2025-07-18
DOI
https://doi.org/10.3390/surfaces8030052
Primary Topic
Microfluidic and Capillary Electrophoresis Applications
Type
article
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article

Buffer pH-Driven Electrokinetic Concentration of Proteins in a Straight Microfluidic Channel

Xavier‐Lewis Palmer, Lanju Mei, Debajit Chakraborty, Diganta Dutta
Surfaces
Microfluidic and Capillary Electrophoresis Applications
article

Buffer pH-Driven Electrokinetic Concentration of Proteins in a Straight Microfluidic Channel

Xavier‐Lewis Palmer, Lanju Mei, Debajit Chakraborty, Diganta Dutta
article en

Abstract

We present a buffer-pH-modulated electrokinetic concentration strategy in MEMS microchannels that harnesses simple pH shifts to neutralize and charge proteins, reversibly “pausing” them at a planar electric-gate electrode by tuning to their isoelectric point (pI) and mobilizing them with slight pH offsets under an applied field. This synergistic coupling of dynamic pH control and electrode-gated focusing, which requires only buffer composition changes, enables rapid and tunable protein capture and release across diverse channel geometries for lab-on-chip, preparative, and point-of-care diagnostics. Moreover, it dovetails with established MEMS biomedical platforms ranging from diagnostics to drug delivery and microsurgery to gene and cell-manipulation devices. Future work on tailored electrode coatings and optimized channel profiles will further boost selectivity, speed, and integration in sub-100 µm MEMS devices.

SurfacesVol. 8(3)
University of Maryland Eastern Shore (US), University of Nebraska at Kearney (US), Old Dominion University (US)
Good health and well-being
Openalex Percentile: Top 81%
Microfluidic and Capillary Electrophoresis Applications
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