pH-Responsive Gamma-Irradiated Poly(Acrylic Acid)-Cellulose-Nanocrystal-Reinforced Hydrogels

A pH-sensitive poly(acrylic acid) composite hydrogel was successfully synthesized via gamma irradiation and reinforced with cellulosic materials of different sizes. Cellulose was extracted from rice husks via alkali and bleaching treatment, and an acid hydrolysis treatment was performed to extract cellulose nanocrystals (CNCs). Morphological observation of cellulose and CNCs using scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed diameters of 22–123 μm and 5–16 nm, respectively. The swelling properties of the fabricated poly(acrylic acid)/cellulosic hydrogels were found to respond to changes in pH, and CNC-reinforced hydrogels performed better than cellulose-reinforced hydrogels. The highly crystalline CNC provided a greater storage modulus, hence acting as a better reinforcing material for poly(acrylic acid)-based hydrogels. SEM showed that hydrogels reinforced with the CNC nanofillers contained a homogeneous pore distribution and produced better interfacial interactions than those reinforced with the cellulose microfillers, thus performing better as hydrogels. These findings demonstrate that gamma-irradiated poly(acrylic acid) hydrogels reinforced with CNCs exhibit a better stimuli response toward pH than poly(acrylic acid) hydrogels reinforced with cellulose

Gamma Irradiation-Assisted Synthesis of Cellulose Nanocrystal-Reinforced Gelatin Hydrogels

Herein, we describe the use of gamma irradiation to prepare hydrogels comprising α-cellulose and cellulose nanocrystal (CNC)-reinforced gelatin in the absence of crosslinking agents. In this study, cellulose was extracted from rice husks by an alkali and bleaching treatment followed by acid hydrolysis to produce CNC. A semi-interpenetrating network (semi-IPN) of hydrogels was developed by the miscibility between gelatin and cellulosic materials. Compared to those prepared from α-cellulose, hydrogels prepared by dispersion of CNCs exhibited remarkably enhanced stiffness and swelling properties, which was ascribed to the uniform distribution of CNCs and their increased crystallinity. Improved pore structure, arrangement, and rigidity of CNC-reinforced gelatin hydrogels, which induced the swelling mechanism resulting in higher and faster water uptake was observed with a scanning electron microscope (SEM), compared to cellulose-reinforced gelatin hydrogels. Moreover, in vitro drug profiling demonstrated that CNC/gelatin hydrogels exhibit good drug loading/release behavior and are thus suitable for use in drug-delivery applications