1. Tailoring the Dependency between Rigidity and WaterUptake of a Microfabricated Hydrogel with the Conformational Rigidityof a Polymer Cross-Linker.
- Author
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Schmidt, John J., Jeong, Jae Hyun, Chan, Vincent, Cha, Chaenyung, Baek, Kwanghyun, Lai, Mei-Hsiu, Bashir, Rashid, and Kong, Hyunjoon
- Subjects
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MICROFABRICATION , *GEOMETRIC rigidity , *HYDROGELS , *CONFORMATIONAL analysis , *CROSSLINKED polymers , *HYDROPHOBIC compounds - Abstract
Many diverse applications utilizehydrogels as carriers, sensors,and actuators, and these applications rely on the refined controlof physical properties of the hydrogel, such as elastic modulus anddegree of swelling. Often, hydrogel properties are interdependent;for example, when elastic modulus is increased, degree of swellingis decreased. Controlling these inverse dependencies remains a majorbarrier for broader hydrogel applications. We hypothesized that polymercross-linkers with varied chain flexibility would allow us to tunethe inverse dependency between the elastic modulus and the degreeof swelling of the hydrogels. We examined this hypothesis by usingalginate and poly(acrylic acid) (PAA) modified with a controlled numberof methacrylic groups as model inflexible and flexible cross-linkers,respectively. Interestingly, the polyacrylamide hydrogel cross-linkedby the inflexible alginate methacrylates exhibited less dependencybetween the degree of swelling and the elastic modulus than the hydrogelcross-linked by flexible PAA methacrylates. This critical role ofthe cross-linker’s inflexibility was related to the differenceof the degree of hydrophobic association between polymer cross-linkers,as confirmed with pyrene probes added in pregel solutions. Furthermore,hydrogels cross-linked with alginate methacrylates could tune theprojection area of adhered cells by solely altering elastic moduli.In contrast, gels cross-linked with PAA methacrylates failed to modulatethe cellular adhesion morphology due to a lower, and smaller, elasticmodulus range to be controlled. Overall, the results of this studywill significantly advance the controllability of hydrogel propertiesand greatly enhance the performance of hydrogels in various biologicalapplications. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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