自愈水凝胶
硅酮
有机硅水凝胶
挤压
硅油
材料科学
弹性体
弹性聚硅酮类
聚合物
粘度
3D打印
高分子科学
互穿聚合物网络
高分子化学
复合材料
眼科
医学
隐形眼镜
作者
Sayan Ganguly,David Wulff,Chau-Minh Phan,Lyndon Jones,Xiaowu Tang
标识
DOI:10.1021/acsabm.4c00901
摘要
While silicone elastomers have found widespread use in the biomedical industry, 3D printing them has proven to be difficult due to the material's slow drying time, low viscosity, and hydrophobicity. Herein, we arrested the hydrophilic silicone (HS) macrochains into a semi-interpenetrating polymer network (semi-IPN) via an in situ photogelation-assisted 3D microextrusion printing technique. The flow behavior of the pregel solutions and the mechanical properties of the printed HS hydrogels were tested, showing a high elastic modulus (approximately 15 kPa), a low tan δ, high elasticity, and delayed network rupturing. The uniaxial compression tests demonstrated a nearly negligible permanent deformation, suggesting that the printed hybrid hydrogel maintained its elastic properties. Drug loading and diffusion in the microporous hydrogel are shown via the non-Fickian anomalous transport mechanism, leading to highly tunable loading/releasing profiles (approximately 20% cumulative release) depending on the HS concentration. The drug encapsulation exhibits exceptional stability, remaining intact without any degradation even after a storage period of 1 month. As far as we know, this is the first soft biomaterial based on HS that functions as an exceptional controlled drug delivery device.
科研通智能强力驱动
Strongly Powered by AbleSci AI