弹性体
材料科学
微尺度化学
聚酯纤维
固化(化学)
聚合物
单体
复合材料
化学工程
纳米技术
数学
工程类
数学教育
作者
Locke Davenport Huyer,Dawn Bannerman,Yufeng Wang,Houman Savoji,Ericka J. Knee‐Walden,Amanda Brissenden,Bess Yee,Mohammad Shoaib,Erin R. Bobicki,Brian G. Amsden,Milica Radisic
标识
DOI:10.1002/adhm.201900245
摘要
Abstract Synthetic polyester elastomeric constructs have become increasingly important for a range of healthcare applications, due to tunable soft elastic properties that mimic those of human tissues. A number of these constructs require intricate mechanical design to achieve a tunable material with controllable curing. Here, the synthesis and characterization of poly(itaconate‐ co‐ citrate‐ co‐ octanediol) (PICO) is presented, which exhibits tunable formation of elastomeric networks through radical crosslinking of itaconate in the polymer backbone of viscous polyester gels. Through variation of reaction times and monomer molar composition, materials with modulation of a wide range of elasticity (36–1476 kPa) are generated, indicating the tunability of materials to specific elastomeric constructs. This correlated with measured rapid and controllable gelation times. As a proof of principle, scaffold support for cardiac tissue patches is developed, which presents visible tissue organization and viability with appropriate elastomeric support from PICO materials. These formulations present potential application in a range of healthcare applications with requirement for elastomeric support with controllable, rapid gelation under mild conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI