Journal of Polymer & Composites Original Research Special issue
Synthesis and Characterization of pH-Sensitive Poly (N-isopropylacrylamide-co-acrylic Acid) Hydrogels for Controlled Release of Doxorubicin
Abstract
pH-responsive polymeric hydrogels have attracted significant attention as intelligent biomaterials for site-specific and controlled drug delivery in cancer therapy due to their ability to respond to the acidic tumor microenvironment. In the present study, poly (N-isopropylacrylamide-co-acrylic acid) [P(NIPAM-co-AAc)] hydrogels were synthesized via free radical copolymerization and systematically characterized to evaluate their suitability for controlled delivery of doxorubicin, a widely used chemotherapeutic agent. The copolymer hydrogels were prepared using N-isopropylacrylamide and acrylic acid as monomers, N,N′-methylenebisacrylamide as a crosslinking agent, and ammonium persulfate as a thermal initiator. The formation and structural integrity of the hydrogels were confirmed by Fourier transform infrared spectroscopy, while thermal behavior was assessed using differential scanning calorimetry. Surface morphology and internal network structure were examined by scanning electron microscopy, revealing a porous architecture favorable for drug loading and diffusion. Swelling studies demonstrated pronounced pH-dependent behavior, with significantly higher swelling ratios under mildly acidic conditions compared to physiological pH, confirming the successful incorporation of pH-responsive functional groups. Doxorubicin loading efficiency was determined using equilibrium swelling methods, and in vitro release studies were conducted at pH 7.4 and 5.5 to simulate normal physiological and tumor microenvironments, respectively. The release profiles indicated sustained and controlled drug release over an extended period, with accelerated release under acidic conditions due to enhanced network expansion. The release kinetics suggested diffusion-controlled and swelling-assisted mechanisms. Overall, the findings demonstrate that P(NIPAM-co-AAc) hydrogels exhibit desirable physicochemical properties, efficient drug encapsulation, and pH-triggered release behavior, highlighting their potential as promising carriers for targeted and controlled anticancer drug delivery applications.
Keywords
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