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Design of therapeutic biomaterials to control inflammation.
Tu, Zhaoxu; Zhong, Yiling; Hu, Hanze; Shao, Dan; Haag, Rainer; Schirner, Michael; Lee, Jaewoo; Sullenger, Bruce; Leong, Kam W.
  • Tu Z; School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China.
  • Zhong Y; Department of Biomedical Engineering, Columbia University, New York, NY USA.
  • Hu H; National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou, China.
  • Shao D; Department of Biomedical Engineering, Columbia University, New York, NY USA.
  • Haag R; School of Chemistry, University of New South Wales, Sydney, New South Wales Australia.
  • Schirner M; Department of Biomedical Engineering, Columbia University, New York, NY USA.
  • Lee J; School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China.
  • Sullenger B; Institutes for Life Sciences, School of Medicine, South China University of Technology, Guangzhou, China.
  • Leong KW; National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou, China.
Nat Rev Mater ; 7(7): 557-574, 2022.
Article en En | MEDLINE | ID: mdl-35251702
Inflammation plays an important role in the response to danger signals arising from damage to our body and in restoring homeostasis. Dysregulated inflammatory responses occur in many diseases, including cancer, sepsis and autoimmunity. The efficacy of anti-inflammatory drugs, developed for the treatment of dysregulated inflammation, can be potentiated using biomaterials, by improving the bioavailability of drugs and by reducing side effects. In this Review, we first outline key elements and stages of the inflammatory environment and then discuss the design of biomaterials for different anti-inflammatory therapeutic strategies. Biomaterials can be engineered to scavenge danger signals, such as reactive oxygen and nitrogen species and cell-free DNA, in the early stages of inflammation. Materials can also be designed to prevent adhesive interactions of leukocytes and endothelial cells that initiate inflammatory responses. Furthermore, nanoscale platforms can deliver anti-inflammatory agents to inflammation sites. We conclude by discussing the challenges and opportunities for biomaterial innovations in addressing inflammation.
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