光引发剂
光子上转换
自愈水凝胶
纳米-
红外线的
固化(化学)
化学
化学工程
高分子化学
光致聚合物
材料科学
聚合
复合材料
有机化学
聚合物
光学
单体
离子
物理
工程类
作者
Xiong Xiao,Ziwei Huang,Hongying Duan,Liping Yang,Yu-Chu Yang,Yushang Lai,Chenxi Li,Li Feng
标识
DOI:10.1021/acs.biomac.4c01775
摘要
In vivo three-dimensional (3D) bioprinting is a promising strategy that can enable personalized organ repair with minimal injury. The current in vivo 3D bioprinting based on upconversion nanoparticles (UCNPs) mediating near-infrared (NIR) light curing is still limited by the low hydrogel cross-linking efficiency. Herein, we introduced a bioink system that allows enhanced NIR light curing by utilizing thiol-ene cross-linkable polymers and photoinitiator-modified UCNPs@LAP nano initiator. The norbornene functionalized hyaluronic acid (NorHA) and thiolated gelatin (GelSH) were first synthesized to prepare the thiol-ene polymer solution. Compared to radical cross-linkable gelatin methacryloyl (GelMA), the NorHA/GelSH exhibited much higher reactivity under weak photoinitiating conditions. With the addition of surface-modified UCNPs@LAP nano initiator, the bioinks showed improved NIR curing performances, which is beneficial to reduce potential thermal damage. Furthermore, in vitro evaluation showed that the NIR light-cured 3D scaffolds preserved excellent bioactivity, suggesting that the hybrid bioink holds great promise to serve as a candidate for in vivo 3D bioprinting.
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