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Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement
Polyalkenoate cement (PAC) is a promising material for regenerative hard tissue therapy. The ionically rich glass component of PAC encourages bioactive interaction via. the release of essential ions. However, PAC bioactivity is restricted owing to (i) structurally inherent cationic network formers a...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897648/ https://www.ncbi.nlm.nih.gov/pubmed/35310353 http://dx.doi.org/10.1016/j.bioactmat.2021.11.020 |
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author | Kim, Ji-Yeong Choi, Woojin Mangal, Utkarsh Seo, Ji-Young Kang, Tae-Yun Lee, Joohee Kim, Taeho Cha, Jung-Yul Lee, Kee-Joon Kim, Kwang-Mahn Kim, Jin-Man Kim, Dohyun Kwon, Jae-Sung Hong, Jinkee Choi, Sung-Hwan |
author_facet | Kim, Ji-Yeong Choi, Woojin Mangal, Utkarsh Seo, Ji-Young Kang, Tae-Yun Lee, Joohee Kim, Taeho Cha, Jung-Yul Lee, Kee-Joon Kim, Kwang-Mahn Kim, Jin-Man Kim, Dohyun Kwon, Jae-Sung Hong, Jinkee Choi, Sung-Hwan |
author_sort | Kim, Ji-Yeong |
collection | PubMed |
description | Polyalkenoate cement (PAC) is a promising material for regenerative hard tissue therapy. The ionically rich glass component of PAC encourages bioactive interaction via. the release of essential ions. However, PAC bioactivity is restricted owing to (i) structurally inherent cationic network formers and (ii) surface bacterial biofilm formation. These two factors cause a deficiency in ion release, further complicated by secondary infections and premature therapeutic failure. Here, a multivalent zwitterionic network modifier (mZM) is presented for upregulation of ionic exchange and bioactivity enhancement. By introducing a non-zero charged mZM into PACs, an increase in the proportion of non-bridging oxygen occurs. The network modification promotes ion channel formation, causing a multiple-fold increase in ion release and surface deposition of hydroxy-carbonate apatite (ca. 74%). Experiments ex vivo and animal models also demonstrate the efficient remineralization ability of the mZM. Furthermore, divalent cationic interaction results in bacterial biofilm reduction (ca. 68%) while also influencing a shift in the biofilm species composition, which favors commensal growth. Therefore, PAC modification with mZM offers a promising solution for upregulation of bioactivity, even aiding in customization by targeting site-specific regenerative therapy in future applications. |
format | Online Article Text |
id | pubmed-8897648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-88976482022-03-17 Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement Kim, Ji-Yeong Choi, Woojin Mangal, Utkarsh Seo, Ji-Young Kang, Tae-Yun Lee, Joohee Kim, Taeho Cha, Jung-Yul Lee, Kee-Joon Kim, Kwang-Mahn Kim, Jin-Man Kim, Dohyun Kwon, Jae-Sung Hong, Jinkee Choi, Sung-Hwan Bioact Mater Article Polyalkenoate cement (PAC) is a promising material for regenerative hard tissue therapy. The ionically rich glass component of PAC encourages bioactive interaction via. the release of essential ions. However, PAC bioactivity is restricted owing to (i) structurally inherent cationic network formers and (ii) surface bacterial biofilm formation. These two factors cause a deficiency in ion release, further complicated by secondary infections and premature therapeutic failure. Here, a multivalent zwitterionic network modifier (mZM) is presented for upregulation of ionic exchange and bioactivity enhancement. By introducing a non-zero charged mZM into PACs, an increase in the proportion of non-bridging oxygen occurs. The network modification promotes ion channel formation, causing a multiple-fold increase in ion release and surface deposition of hydroxy-carbonate apatite (ca. 74%). Experiments ex vivo and animal models also demonstrate the efficient remineralization ability of the mZM. Furthermore, divalent cationic interaction results in bacterial biofilm reduction (ca. 68%) while also influencing a shift in the biofilm species composition, which favors commensal growth. Therefore, PAC modification with mZM offers a promising solution for upregulation of bioactivity, even aiding in customization by targeting site-specific regenerative therapy in future applications. KeAi Publishing 2021-11-20 /pmc/articles/PMC8897648/ /pubmed/35310353 http://dx.doi.org/10.1016/j.bioactmat.2021.11.020 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kim, Ji-Yeong Choi, Woojin Mangal, Utkarsh Seo, Ji-Young Kang, Tae-Yun Lee, Joohee Kim, Taeho Cha, Jung-Yul Lee, Kee-Joon Kim, Kwang-Mahn Kim, Jin-Man Kim, Dohyun Kwon, Jae-Sung Hong, Jinkee Choi, Sung-Hwan Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
title | Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
title_full | Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
title_fullStr | Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
title_full_unstemmed | Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
title_short | Multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
title_sort | multivalent network modifier upregulates bioactivity of multispecies biofilm-resistant polyalkenoate cement |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897648/ https://www.ncbi.nlm.nih.gov/pubmed/35310353 http://dx.doi.org/10.1016/j.bioactmat.2021.11.020 |
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