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    Area of Science:

    • Biomaterials Science
    • Nanotechnology
    • Surface Chemistry

    Background:

    • Developing selective adsorbents for biomolecules is crucial for diagnostics and purification.
    • Zwitterionic polymers offer excellent biocompatibility and antifouling properties.
    • Magnetic nanoparticles (NPs) provide a versatile platform for separation and sensing applications.

    Purpose of the Study:

    • To fabricate and characterize zwitterionic polymer-modified magnetic nanoparticles (NPs) for selective biomolecule adsorption.
    • To compare the performance of one-step (1S NPs) and two-step (2S NPs) fabrication methods.
    • To investigate the specificity of the developed NPs towards Immunoglobulin G (IgG) in complex biological environments.

    Main Methods:

    • Conjugation of poly(sulfobetaine methacrylate) (pSBMA) onto polyethyleneimine (PEI)-precoated magnetic NPs using divinyl sulfone as a linker.
    • Fabrication of 1S NPs (one-step) and 2S NPs (two-step) with varying surface chemistries.
    • Characterization of NP properties and assessment of IgG and Bovine Serum Albumin (BSA) adsorption in serum mixtures.

    Main Results:

    • Both 1S and 2S NPs demonstrated resistance to non-specific protein adsorption (IgG and BSA).
    • 2S NPs exhibited significant specificity for IgG adsorption in complex biological fluids, such as serum mixtures.
    • The binding affinity (Kd ≈ 1.2 μM) of IgG to 2S NPs was moderate, significantly lower than IgG-Protein A interactions (Kd 10 nM).
    • IgG specificity of 2S NPs was attributed to the combination of short-chain polyzwitterions and high-density sulfone groups.

    Conclusions:

    • The two-step fabrication method successfully produced zwitterionic magnetic nanoparticles with high specificity for IgG.
    • The developed NPs show potential for selective capture of IgG in complex biological samples.
    • Surface characteristics, including polyzwitterion chain length and sulfone group density, are critical for achieving targeted biomolecule recognition.