Microfluidic-assisted polymer-protein assembly to fabricate homogeneous functionalnanoparticles
Libo Zhang1, Andrew Beatty1, Lin Lu1
1Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, SC 29208, USA.
Summary
Electrokinetics-driven microfluidics enable rapid, homogeneous assembly of functional polymer-protein nanoparticles (NPs). This method improves NP size distribution and preserves protein functionality, offering a novel approach for nanotechnology applications.
Area of Science:
- Biotechnology and Nanotechnology
- Materials Science
- Chemical Engineering
Background:
- Functional polymer-protein nanoparticles (NPs) are crucial for diverse biotechnological and nanotechnological applications.
- Conventional bulk synthesis methods struggle to achieve the homogeneous mixing required for uniform NP fabrication.
- Controllable and vigorous mixing is essential for creating well-defined polymer-protein nanostructures.
Purpose of the Study:
- To explore an electrokinetics (EK)-based microfluidic reactor for assembling functional proteins with polymers.
- To investigate the efficiency of fast mixing in producing homogeneous polymer-protein NPs.
- To assess the impact of the microfluidic method on NP size distribution and protein functionality.
Main Methods:
- Utilized an electrokinetics (EK)-based microfluidic reactor for rapid mixing of polymers and functional proteins.
- Employed an ethanol/water co-solvent system for nanoparticle assembly.
- Varied the mass ratio of polymer to protein to tune nanoparticle size.
Main Results:
- Achieved significantly improved size distribution of polymer-protein NPs compared to conventional bulk methods.
- Demonstrated tunability of NP size by adjusting the polymer-to-protein mass ratio.
- Confirmed sustained functionality of assembled proteins after microfluidic processing.
Conclusions:
- EK-based microfluidic mixing offers a superior method for fabricating homogeneous polymer-protein NPs.
- The microfluidic approach provides control over NP size and preserves protein activity.
- This method holds significant potential for the controlled assembly of various functional proteins in nanotechnology.


