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30秒内无光引发剂的可见光激光直写高分辨率、生物相容性、超多功能且坚韧的水凝胶

Visible light laser direct-writing of high-resolution, biocompatible, super-multifunctional and tough hydrogels without photoinitiators in 30 s.

作者信息

Li Zhangkang, He Xiao, Kumar Hitendra, Shin Jaemyung, Guo Chijie, Abraham Brett, Shayesteh Ali, Kibria Md, Lu Qingye, Bai Huiyu, Kim Keekyoung, Hu Jinguang

机构信息

Department of Biomedical Engineering, University of Calgary, 2500 University Dr. NW, Calgary, Alberta T2N 1N4, Canada.

Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Drive, NW, Calgary T2N 1N4, Alberta, Canada.

出版信息

Biomater Adv. 2023 Apr;147:213318. doi: 10.1016/j.bioadv.2023.213318. Epub 2023 Feb 1.

DOI:10.1016/j.bioadv.2023.213318
PMID:36746100
Abstract

Currently, the lack of bioinks and long printing time limits the further development of biofabrication. Here we report a novel biocompatible, multi-functional and tough 3D printable hydrogel via visible light photocrosslinking of polyvinyl alcohol bearing styrylpyridinium group (PVA-SbQ). The high-resolution PVA-SbQ hydrogels with different designed shapes can be generated via laser direct-writing in 30 s without extra toxic crosslinkers or photoinitiators, and demonstrates excellent biocompatibility. The rapid laser direct-writing technology also results in a super-strong, tough hydrogel with excellent adhesive, swelling, self-healing, and photo-tunable properties due to the photodimerization of styrylpyridinium (SbQ) groups and the left-over massive amount of free hydroxyl groups in the hydrogel. For example, the maximum tensile strength, elongation, compressive strength adhesive strength of printed PVA-SbQ hydrogels can reach 1.0 MPa, 810 %, 33 MPa, 31 kPa, and 25,000 % respectively. And these properties can be adjusted by controlling the parameters for laser direct-writing. In addition, the introduced nitrogen cations by SbQ groups further endow hydrogels with the potential to develop novel functionality, which is demonstrated by integrating negatively charged nanocelluloses in the PVA-SbQ system to develop underwater adhesives, anti-freezing (-24.9 °C), and anti-bacterial hydrogels. This discovery opens multiple doors for developing PVA-SbQ based multi-functional hydrogel for various applications including biofabrication and tissue engineering.

摘要

目前,生物墨水的缺乏和较长的打印时间限制了生物制造的进一步发展。在此,我们报道了一种通过含苯乙烯基吡啶鎓基团的聚乙烯醇(PVA-SbQ)的可见光光交联制备的新型生物相容性、多功能且坚韧的3D可打印水凝胶。具有不同设计形状的高分辨率PVA-SbQ水凝胶可通过激光直写在30秒内生成,无需额外的有毒交联剂或光引发剂,并且具有优异的生物相容性。这种快速激光直写技术还由于苯乙烯基吡啶鎓(SbQ)基团的光二聚作用以及水凝胶中大量剩余的游离羟基,产生了一种具有超强、坚韧特性以及优异的粘附性、溶胀性、自愈性和光可调性的水凝胶。例如,打印的PVA-SbQ水凝胶的最大拉伸强度、伸长率、抗压强度、粘附强度分别可达1.0 MPa、810%、33 MPa、31 kPa和25000%。并且这些性能可以通过控制激光直写的参数来调节。此外,SbQ基团引入的氮阳离子进一步赋予水凝胶开发新功能的潜力,这通过在PVA-SbQ体系中整合带负电荷的纳米纤维素来开发水下粘合剂、抗冻(-24.9°C)和抗菌水凝胶得以证明。这一发现为开发基于PVA-SbQ的多功能水凝胶用于包括生物制造和组织工程在内的各种应用打开了多扇大门。

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