Bio-inspired poly-DL-serine materials resist the foreign-body response

Implantation-caused foreign-body response (FBR) is a commonly encountered issue and can result in failure of implants. The high L-serine content in low immunogenic silk sericin, and the high D-serine content as a neurotransmitter together inspire us to prepare poly-DL-serine (PSer) materials in miti...

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Published inNature communications Vol. 12; no. 1; pp. 5327 - 12
Main Authors Zhang, Donghui, Chen, Qi, Bi, Yufang, Zhang, Haodong, Chen, Minzhang, Wan, Jianglin, Shi, Chao, Zhang, Wenjing, Zhang, Junyu, Qiao, Zhongqian, Li, Jin, Chen, Shengfu, Liu, Runhui
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.09.2021
Nature Publishing Group
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Summary:Implantation-caused foreign-body response (FBR) is a commonly encountered issue and can result in failure of implants. The high L-serine content in low immunogenic silk sericin, and the high D-serine content as a neurotransmitter together inspire us to prepare poly-DL-serine (PSer) materials in mitigating the FBR. Here we report highly water soluble, biocompatible and easily accessible PSer hydrogels that cause negligible inflammatory response after subcutaneous implantation in mice for 1 week and 2 weeks. No obvious collagen capsulation is found surrounding the PSer hydrogels after 4 weeks, 3 months and 7 months post implantation. Histological analysis on inflammatory cytokines and RNA-seq assay both indicate that PSer hydrogels show low FBR, comparable to the Mock group. The anti-FBR performance of PSer hydrogels at all time points surpass the poly(ethyleneglycol) hydrogels that is widely utilized as bio-inert materials, implying the potent and wide application of PSer materials in implantable biomaterials and biomedical devices. Implantation-caused foreign-body response is a commonly encountered issue and can result in failure of implants. Here, the authors demonstrate that a highly water soluble, biocompatible, and easily accessible poly-DL-serine hydrogel can mitigate foreign-body response.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-021-25581-9