Main content area

Polydopamine functionalized hydrogel beads as magnetically separable antibacterial materials

Matai, Ishita, Garg, Mayank, Rana, Kajal, Singh, Suman
RSC advances 2019 v.9 no.24 pp. 13444-13457
Escherichia coli, Fourier transform infrared spectroscopy, Listeria monocytogenes, Staphylococcus aureus, X-ray diffraction, alginates, antibiotics, crosslinking, fluorescence, granules, hydrogels, hydrophilicity, magnetism, magnetite, nanoparticles, scanning electron microscopy, staining, storage modulus, transmission electron microscopy, viscosity, wettability
In the present study, magnetically separable hydrogel beads of ionically cross-linked alginate were functionalized with polydopamine (PDA). The rationale behind this was to enhance the structural stability and antibacterial profile of PDA/Alg/Fe₃O₄ beads (K3). Incorporation of superparamagnetic magnetite (Fe₃O₄) nanoparticles endowed the hydrogel beads with magnetism. X-ray diffraction (XRD) analysis revealed the successful formation of pure Alg/Fe₃O₄ nanoparticles having an inverse spinel structure. Vibrating sample magnetometry (VSM) confirmed their superparamagnetic behaviour with Mₛ values of 36.18 and 30.46 emu g⁻¹ at 5 and 300 K, respectively. High resolution-transmission electron microscopy (HR-TEM) images showed alginate capping and the size of the Alg/Fe₃O₄ nanoparticles (∼8 nm). The successful deposition of PDA granules on the K3 bead surface was verified by field emission-scanning electron microscopy (FE-SEM). The PDA functionalization was further justified by VSM, XRD and Fourier-transform infrared spectroscopy (FT-IR). During swelling experiments, K3 beads displayed appreciable structural stability compared to bare/non-functionalized beads. Wettability studies revealed K3 beads to be hydrophilic with a contact angle of ∼55°. Rheological parameters including storage modulus (G′) and shear viscosity of K3 increased upon PDA functionalization. During antibacterial tests, K3 strongly inhibited E. coli, S. typhi, S. aureus and L. monocytogenes in a concentration and time dependent manner. Fluorescence staining experiments showed that K3 could greatly alter the bacterial membrane integrity. Reusability experiments with K3 beads substantiated their effective broad-spectrum antibacterial performance for three consecutive cycles.