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Penetrating Macrophage-Based Nanoformulation for Periodontitis Treatment.
Yan, Na; Xu, Junchao; Liu, Guolin; Ma, Chao; Bao, Lin; Cong, Yalin; Wang, Ziyao; Zhao, Yuliang; Xu, Weihua; Chen, Chunying.
Afiliación
  • Yan N; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing100190, P. R. China.
  • Xu J; University of Chinese Academy of Sciences, Beijing100049, P. R. China.
  • Liu G; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing100190, P. R. China.
  • Ma C; University of Chinese Academy of Sciences, Beijing100049, P. R. China.
  • Bao L; Liangxiang Hospital, Capital Medical University, Beijing100024, P. R. China.
  • Cong Y; Peking Union Medical College Hospital, Beijing100032, P. R. China.
  • Wang Z; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing100190, P. R. China.
  • Zhao Y; University of Chinese Academy of Sciences, Beijing100049, P. R. China.
  • Xu W; CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing100190, P. R. China.
  • Chen C; University of Chinese Academy of Sciences, Beijing100049, P. R. China.
ACS Nano ; 16(11): 18253-18265, 2022 11 22.
Article en En | MEDLINE | ID: mdl-36288552
Periodontitis is a chronic inflammatory disease caused by the interaction of oral microorganisms with the host immune response. Porphyromonas gingivalis (P.g.) acts as a key mediator in subverting the homeostasis of the local immune system. On the one hand, P.g. inhibits phagocytosis and the killing capacity of immune cells. On the other hand, P.g. increases selective cytokine release, which is beneficial to its further proliferation. Here, we prepared a penetrating macrophage-based nanoformulation (MZ@PNM)-encapsulating hydrogel (MZ@PNM@GCP) that responded to the periodontitis microenvironment. MZ@PNM targeted P.g. via the Toll-like receptor complex 2/1 (TLR2/1) on its macrophage-mimicking membrane, then directly killed P.g. through disruption of bacterial structural integrity by the cationic nanoparticles and intracellular release of an antibacterial drug, metronidazole (MZ). Meanwhile, MZ@PNM interrupted the specific binding of P.g. to immune cells and neutralized complement component 5a (C5a), preventing P.g. subversion of periodontal host immune response. Overall, MZ@PNM@GCP showed potent efficacy in periodontitis treatment, restoring local immune function and killing pathogenic bacteria, while exhibiting favorable biocompatibility, all of which have been demonstrated both in vivo and in vitro.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Periodontitis Límite: Humans Idioma: En Revista: ACS Nano Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Periodontitis Límite: Humans Idioma: En Revista: ACS Nano Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos