Abstract
ABSTRACTSensitive nanohydrogels were prepared via surfactant free emulsion copolymerization of N‐vinylcaprolactam and poly(ethylene glycol) methyl ether methacrylate, and either N‐vinylpyrrolidone (VP) or 2‐methacryloyloxybenzoic acid (2MBA) to adjust the transition temperature (Ttr). The crosslinker ethylene glycol dimethacrylate was used for the polymer network construction. The resulting nanohydrogel sizes are between 120 and 300 nm. ρ‐Parameter, obtained from light scattering studies, suggests that core‐sell nanogels of flexible chains were obtained. Ttr increases with increasing comonomer content (VP or 2MBA) and decreases with decreasing pH for 2MBA containing nanohydrogels. Nanohydrogels containing 15.5% of 2MBA exhibit Ttr close to 38 °C. Nanogels are able to control the release of the loaded antineoplastic drug 5‐fluorouracil. For the prepared T/pH‐sensitive nanogels, the release is slower at pH 7.4 and 37 °C than at tumor conditions: pH 6 and 40 °C. Mathematical models were applied to evaluate the kinetics of drug release; Peppas model fitted best indicating a Fickian diffusion trough a sphere. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 2662–2672
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More From: Journal of Polymer Science Part A: Polymer Chemistry
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