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Smart superporous hydrogels (SPHs) based on dimethylaminoethyl methacrylate and acrylamide monomers with and without magnetic nanoparticles (MNPs) were synthesized via a microwave procedure. The synthesized samples were confirmed by various techniques such as Fourier transform spectroscopy, x-ray diffraction, thermogravimetric analysis, scanning electron microscopy, vibrating sample magnetometry, and transmission electron microscopy. The parameters such as pH, irradiation time, and MNPs content on the swelling behavior of products were studied. The results of swelling studies in artificial gastric and intestine media exhibited a higher swelling ratio of SPHs in lower pH, confirming smart performance of SPHs for gastroretentive drug delivery (GDD). The metronidazole (MTZ) was used as an effective antibiotic administered in peptic ulcer therapy. The in vitro release studies showed that the presence of MNPs into the hydrogel network provided the sustained release pattern for MTZ. It was concluded that our developed SPHs and MSPHs fabricated via a facile method have potential to be used in GDD. C

Poly (N-isopropylacrylamide-methyl methacrylic acid, PNIPAAm-MAA)-grafted magnetic nanoparticles were synthesized using silane-coated magnetic nanoparticles as a template for radical polymerization of N-isopropylacrylamide and methacrylic acid. Properties of these nanoparticles, such as size, drug-loading efficiency, and drug release kinetics, were evaluated in vitro for targeted and controlled drug delivery. The resulting nanoparticles had a diameter of 100 nm and a doxorubicin-loading efficiency of 75%, significantly higher doxorubicin release at 40°C compared with 37°C, and pH 5.8 compared with pH 7.4, demonstrating their temperature and pH sensitivity, respectively. In addition, the particles were characterized by X-ray powder diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and vibrating sample magnetometry. In vitro cytotoxicity testing showed that the PNIPAAm-MAA-coated magnetic nanoparticles had no cytotoxicity and were biocompatible, indicating their potential for biomedical application.

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