Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules

Abstract Critical bone defects, exacerbated by infections, pose significant challenges to bone healing and homeostasis, necessitating the development of dual-functional biomimetics that combine anti-infective and reparative capabilities. The EGaIn holds promise across various disciplines, though its...

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Main Authors: Kevin H. Mwangi, Yue Qu, Peilun Hu, Toshitatsu Nagayasu, Jia-Feng Liu, Xiumei Wang
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:npj Biofilms and Microbiomes
Online Access:https://doi.org/10.1038/s41522-025-00724-8
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author Kevin H. Mwangi
Yue Qu
Peilun Hu
Toshitatsu Nagayasu
Jia-Feng Liu
Xiumei Wang
author_facet Kevin H. Mwangi
Yue Qu
Peilun Hu
Toshitatsu Nagayasu
Jia-Feng Liu
Xiumei Wang
author_sort Kevin H. Mwangi
collection DOAJ
description Abstract Critical bone defects, exacerbated by infections, pose significant challenges to bone healing and homeostasis, necessitating the development of dual-functional biomimetics that combine anti-infective and reparative capabilities. The EGaIn holds promise across various disciplines, though its interactions with microbial cells require further elucidation. This investigation evaluates the antimicrobial efficacy of PEG-EGaIn nanocapsules against a spectrum of bacterial, employing electron microscopy. Constructs containing 1.5% PEG-EGaIn hinder biofilm-producing bacteria, while 3% concentrations amplify the biocidal effect. Furthermore, the nanocapsules promoted osteogenic differentiation rBMSCs, evidenced by enhanced mineralization and upregulation of key osteogenic genes. In addressing large bone defects, PEG-EGaIn-Col-Ap-lamellar and ethanolic-mediated Col-Ap-lamellar constructs serve as potential solutions for bone resorption mitigation and osteo-angiogenesis. Bone-remodeling were validated through μ-CT and histomorphometry confirming no evidence of chronic inflammation or fibrosis. In this study, PEG-EGaIn nanocapsules emerge as potent biocide and bone repair, underscoring their potential in combating antibiotic resistance and enhancing bone healing.
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issn 2055-5008
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publishDate 2025-07-01
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spelling doaj-art-a9577786b17e464aa3357d43e47ffdf52025-08-20T03:03:38ZengNature Portfolionpj Biofilms and Microbiomes2055-50082025-07-0111111610.1038/s41522-025-00724-8Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsulesKevin H. Mwangi0Yue Qu1Peilun Hu2Toshitatsu Nagayasu3Jia-Feng Liu4Xiumei Wang5State Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua UniversitySchool of Life science, Center of Biology, Tsinghua UniversityState Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua UniversityState Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua UniversityCenter for Infection Biology, School of Basic Medical Science, Tsinghua UniversityState Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua UniversityAbstract Critical bone defects, exacerbated by infections, pose significant challenges to bone healing and homeostasis, necessitating the development of dual-functional biomimetics that combine anti-infective and reparative capabilities. The EGaIn holds promise across various disciplines, though its interactions with microbial cells require further elucidation. This investigation evaluates the antimicrobial efficacy of PEG-EGaIn nanocapsules against a spectrum of bacterial, employing electron microscopy. Constructs containing 1.5% PEG-EGaIn hinder biofilm-producing bacteria, while 3% concentrations amplify the biocidal effect. Furthermore, the nanocapsules promoted osteogenic differentiation rBMSCs, evidenced by enhanced mineralization and upregulation of key osteogenic genes. In addressing large bone defects, PEG-EGaIn-Col-Ap-lamellar and ethanolic-mediated Col-Ap-lamellar constructs serve as potential solutions for bone resorption mitigation and osteo-angiogenesis. Bone-remodeling were validated through μ-CT and histomorphometry confirming no evidence of chronic inflammation or fibrosis. In this study, PEG-EGaIn nanocapsules emerge as potent biocide and bone repair, underscoring their potential in combating antibiotic resistance and enhancing bone healing.https://doi.org/10.1038/s41522-025-00724-8
spellingShingle Kevin H. Mwangi
Yue Qu
Peilun Hu
Toshitatsu Nagayasu
Jia-Feng Liu
Xiumei Wang
Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules
npj Biofilms and Microbiomes
title Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules
title_full Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules
title_fullStr Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules
title_full_unstemmed Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules
title_short Microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of PEG EGaIn nanocapsules
title_sort microanatomy related biocidal activity at cellular resolution and bone reconstruction potential of peg egain nanocapsules
url https://doi.org/10.1038/s41522-025-00724-8
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