부산대학교 도서관

Establishing the independent tunability of transport and mechanical properties in polymer gels would significantly contribute to their implementation as transdermal drug delivery media, among other things. The work conducted herein uses facile changes in the formulation of physically crosslinked styrenic ABA/AB block copolymer organogels to alter their mechanical properties independently from the mass transport of an internally‐loaded nanocarrier. Such independent tunability is made possible by altering the relative amounts of ABA triblock and AB diblock copolymers while holding total copolymer concentration fixed. Specifically, three series of gels each with a fixed total copolymer concentration (10, 20, or 30 wt%) comprised of varying triblock copolymer concentration are studied. Small angle x‐ray scattering confirms that, at the nanoscale, only gel network connectivity changes within each series, while mechanical and release experiments show that increasing network connectivity leads to significant growth of gel moduli, but little change in nanocarrier release rate. Simple formulation changes in block copolymer gels can lead to alteration of their properties. Increasing copolymer concentration, for example, typically translates to increased stiffness and strength and decreased release rate of encapsulated payload compounds. In this study, the release rate of nanocarriers within gels and gel’s mechanical behavior are decoupled using a diblock/triblock copolymer blending strategy.