The use of materials to restore or replace the functions of damaged body parts has been proven historically. Any material can be considered as a biomaterial as long as it performs its biological function and does not cause adverse effects to the host. With the increasing demands for biofunctionality, biomaterials nowadays may not only encompass inertness but also specialized utility towards the target biological application. A hydrogel is a biomaterial with a 3D network made of hydrophilic polymers. It is regarded as one of the earliest biomaterials developed for human use. The preparation of hydrogel is often attributed to the polymerization of monomers or crosslinking of hydrophilic polymers to achieve the desired ability to hold large amounts of aqueous solvents and biological fluids. The generation of hydrogels, however, is shifting towards developing hydrogels through the aid of enabling technologies. This review provides the evolution of hydrogels and the different approaches considered for hydrogel preparation. Further, this review presents the plasma process as an enabling technology for tailoring hydrogel properties. The mechanism of plasma-assisted treatment during hydrogel synthesis and the current use of the plasma-treated hydrogels are also discussed.

Polyaniline–chitosan (PAni–Cs) composite films were synthesized using a solution casting method with varying PAni concentrations. Polyaniline powders used in the composite synthesis were polymerized using acetic acid as the dopant media. Raman spectroscopy revealed that the PAni powders synthesized using hydrochloric acid and acetic acid did not exhibit significant difference to the chemical features of PAni, implying that PAni was formed in varying concentrations of the dopant media. The presence of agglomerated particles on the surface of the Cs composite, which may have been due to the presence of PAni powders, was observed with scanning electron microscope–energy dispersive X-ray spectroscopy (SEM–EDX). Ultraviolet–visible (UV–Vis) spectroscopy further showed the interaction of PAni with Cs where the Cs characteristic peak shifted to a higher wavelength. Cell viability assay also revealed that the synthesized PAni–Cs composites were nontoxic and may be utilized for future biomedical applications.

This study explores the effect of atmospheric pressure plasma (APP) treatment on chitosan-acrylic acid (Cs-AA) blends. The experiment involves a custom-built APP setup used to modify a polymeric blend composed of natural (Cs) and synthetic (AA) polymers. Even with a low process temperature (<40 °C), reactive oxygen and nitrogen species (RONS) were observed in an air plasma plume. The interaction of plasma with the liquid surface was also observed. With de-ionized water as the test liquid, the operating parameters such as the treatment time and flow rate were shown to influence the pH and absorption spectrum of the liquid. The presence of RONS was investigated using optical emission spectroscopy coupled with principal component analysis. The analysis revealed that the air plasma contains the different N systems, NO, OH, H α, monatomic N, and monatomic O species. Varying the gas flow rate influences the production of NO and OH radicals while measuring plasma discharge in different conditions (ambient air, DI H 2O, Cs, and Cs-AA blend) affects the concentration of the N positive and negative systems. The effect of these RONS on the Cs-AA blends was also investigated by assessing the chemical structure, pH, and viscosity of the solution. In correlation with all of the findings, it was observed that plasma treatment could degrade pure Cs solution by dehydrogenation and glycosidic bond cleaving. However, the addition of AA reduces the degradation so that the AA radicals created by plasma form a complex with the Cs that reduces Cs fragmentation and chain entanglement, as observed in the reduction of viscosity. In summary, the rich reactive species created by plasma in the Cs-AA solution not only provided stable species but also introduced more Cs-AA complexes.