Injectable biodegradation-visual self-healing citrate hydrogel with high tissue penetration for microenvironment-responsive degradation and local tumor therapy

被引:88
作者
Wang, Min [1 ]
Chen, Mi [1 ]
Niu, Wen [1 ]
Winston, Dagogo Dorothy [1 ]
Cheng, Wei [1 ]
Lei, Bo [1 ,2 ,3 ,4 ]
机构
[1] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710000, Peoples R China
[2] Xi An Jiao Tong Univ, Coll Stomatol, Key Lab Shaanxi Prov Craniofacial Precis Med Res, Xian 710054, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 2, Natl & Local Joint Engn Res Ctr Biodiag & Biother, Xian 710000, Peoples R China
[4] Xi An Jiao Tong Univ, Instrument Anal Ctr, Xian 710054, Peoples R China
基金
中国国家自然科学基金;
关键词
Multifunctional biomaterials; Citric acid polymers; Scaffolds; Biodegradation tracking; Tumor therapy; MESOPOROUS SILICA NANOPARTICLES; REAL-TIME; CARBOXYMETHYL CHITOSAN; NONINVASIVE TRACKING; DELIVERY; ACID; ANTIBACTERIAL; DOXORUBICIN; CARRIER; PHOTOLUMINESCENT;
D O I
10.1016/j.biomaterials.2020.120301
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Local tumor therapy through injectable biodegradable hydrogels with controlled drug release has attracted much attention recently, due to their easy operation, low side effect and efficiency. However, most of the reported therapeutic hydrogel system showed a lack of biodegradation tracking and tumor environment-responsive degradation/therapy. Herein, we developed a multifunctional injectable biodegradation-visual citric acid-based self-healing scaffolds with microenvimnment-responsive degradation and drug release for safe and efficient skin tumor therapy (FPRC hydrogel). FPRC scaffolds possess multifunctional properties including thermosensitive, injectable, self-healing, photoluminescent and pH-responsive degradation/drug release. The FPRC scaffolds with strong red fluorescence which has good photostability, tissue penetration and biocompatibility can be tracked and monitored to evaluate the degradation of the scaffolds in vivo. Moreover, the FPRC scaffolds showed pH-responsive doxorubicin (DOX) release, efficiently killed the A375 cancer cell in vitro and suppressed the tumor growth in vivo. Compared to the free drug (DOX), the FPRC@DOX scaffolds displayed a significantly high therapeutic effect and less biotoxicity. This work provides an alternative strategy to design smart visual scaffolds for tumor therapy and regenerative medicine.
引用
收藏
页数:12
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