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通过可注射的纳米酶功能化水凝胶微球耗尽局部乳酸积累以缓解炎症和促进组织再生。

Exhausted local lactate accumulation via injectable nanozyme-functionalized hydrogel microsphere for inflammation relief and tissue regeneration.

作者信息

Shen Jieliang, Chen Ao, Cai Zhengwei, Chen Zhijie, Cao Ruichao, Liu Zongchao, Li Yuling, Hao Jie

机构信息

Department of Orthopedics, Orthopedic Laboratory of Chongqing Medical University, The First Affiliated Hospital of Chongqing Medical University, No.1 Youyi Road, Chongqing, 40042, PR China.

School of Biomedical Engineering, Shanghai Jiao Tong University, 1954 Huashan Road, Shanghai, 200030, PR China.

出版信息

Bioact Mater. 2021 Oct 21;12:153-168. doi: 10.1016/j.bioactmat.2021.10.013. eCollection 2022 Jun.

Abstract

Local lactate accumulation greatly hinders tissue repair and regeneration under ischemic condition. Herein, an injectable microsphere (MS@MCL) for local lactate exhaustion was constructed by grafting manganese dioxide (MnO) -lactate oxidase (LOX) composite nanozyme on microfluidic hyaluronic acid methacrylate (HAMA) microspheres via chemical bonds, achieving a long-term oxygen-promoted lactate exhaustion effect and a long half-life . The uniform and porous microspheres synthesized by microfluidic technology is beneficial to injection therapy and improving encapsulation efficiency. Furthermore, chemical grafting into HAMA microspheres through amide reactions promoted local enzymatic concentration and activity enhancement. It was showed that the MS@MCL eliminated oxidative and inflammatory stress and promoted extracellular matrix metabolism and cell survival when co-cultured with nucleus pulposus cells (NPCs) . In the rat degenerative intervertebral disc model caused by lactate injection, MS@MCL showed a long-term therapeutic effect in reducing intervertebral height narrowing and preventing extracellular matrix (ECM) degradation as well as inflammatory damage . Altogether, this study confirms that this nanozyme-functionalized injectable MS@MCL effectively improves the regenerative and reparative effect in ischemic tissues by disposing of enriched lactate in local microenvironment.

摘要

局部乳酸积累在缺血条件下极大地阻碍了组织修复和再生。在此,通过化学键将二氧化锰(MnO)-乳酸氧化酶(LOX)复合纳米酶接枝到微流控甲基丙烯酸透明质酸(HAMA)微球上,构建了一种用于局部清除乳酸的可注射微球(MS@MCL),实现了长期的氧促进乳酸清除效果和较长的半衰期。通过微流控技术合成的均匀且多孔的微球有利于注射治疗并提高包封效率。此外,通过酰胺反应化学接枝到HAMA微球中促进了局部酶浓度和活性的增强。结果表明,MS@MCL与髓核细胞(NPCs)共培养时可消除氧化应激和炎症应激,并促进细胞外基质代谢和细胞存活。在乳酸注射所致的大鼠退变椎间盘模型中,MS@MCL在减轻椎间盘高度狭窄、防止细胞外基质(ECM)降解以及炎症损伤方面显示出长期治疗效果。总之,本研究证实这种纳米酶功能化的可注射MS@MCL通过清除局部微环境中富集的乳酸,有效改善了缺血组织中的再生和修复效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ba5/8897073/1f7047753c08/ga1.jpg

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