Photo-initiated enhanced antibacterial therapy using a non-covalent functionalized graphene oxide nanoplatform
This study describes a novel antibacterial phototherapeutic platform for highly efficient healing of bacteria-infected wounds. It is based on the photodynamic and physical actions of a zinc tetraaminophthalocyanine-modified graphene oxide nanocomposite produced via non-covalent functionalization. Th...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2021-06, Vol.5 (24), p.844-8412 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This study describes a novel antibacterial phototherapeutic platform for highly efficient healing of bacteria-infected wounds. It is based on the photodynamic and physical actions of a zinc tetraaminophthalocyanine-modified graphene oxide nanocomposite produced
via
non-covalent functionalization. The nanocomposite is positively charged and can easily capture negatively charged bacteria
via
electrostatic interactions. The antibacterial action is two-fold: (1) reactive oxygen species are produced by the phthalocyanine photosensitizer after short-term exposure to 680 nm light and (2) the graphene oxide can physically cut bacterial cell membranes. These enhanced activities can kill Gram-positive and Gram-negative bacteria at very low dosages. An ultrastructural examination indicates that this nanocomposite causes enormous damage to bacterial morphology and leakage of intracellular substances that lead to bacterial death. A rat wound model is used to demonstrate that the proposed phototherapeutic platform has low cytotoxicity and can promote rapid healing in bacteria-infected wounds. These results suggest that the integration of different antibacterial methods into a single nanotherapeutic platform is a promising strategy for anti-infective treatment.
A non-covalent functionalized graphene oxide nanoplatform can kill bacteria at very low dosages and promote rapid healing of bacteria-infected wounds. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/d1dt00642h |