Noninvasive photothermal therapy (PTT) is an emerging strategy for eliminating multidrug-resistant (MDR) bacteria that achieve sterilization by generating temperatures above 50 °C; however, such a high temperature also causes collateral damage to healthy tissues. In this study, we developed a low-temperature PTT based on borneol-containing polymer-modified MXene nanosheets (BPM) with bacteria-targeting capabilities. BPM was fabricated through the electrostatic coassembly of negatively charged two-dimensional MXene nanosheets (2DM) and positively charged quaternized α-(+)-borneol-poly(N,N-dimethyl ethyl methacrylate) (BPQ) polymers. Integrating BPQ with 2DM improved the stability of 2DM in physiological environments and enabled the bacterial membrane to be targeted due to the presence of a borneol group and the partially positive charge of BPQ. With the aid of near-infrared irradiation, BPM was able to effectively eliminate methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli) through targeted photothermal hyperthermia. More importantly, BPM effectively eradicated more than 99.999% (>5 orders of magnitude) of MRSA by localized heating at a temperature that is safe for the human body (≤40 °C). Together, these findings suggest that BPM has good biocompatibility and that membrane-targeting low-temperature PTT could have great therapeutic potential against MDR infections.
Photothermal therapy is an ideal non-invasive treatment for bacterial infections. However, if the photothermal agents are unable to target bacteria, it can also cause thermal damage to healthy tissue. This...
Antibacterial cotton helps prevent the growth and spread of harmful microorganisms, reduces the risk of infection, and has a prolonged service life by reducing bacterial degradation. However, most antibacterial agents used are toxic to humans and the environment. Citronellol‐poly(N,N‐dimethyl ethyl methacrylate) (CD), a highly effective antibacterial polymer, is synthesized from natural herbal essential oils (EOs). CD exhibited efficient, rapid bactericidal activity against Gram‐positive, Gram‐negative, and drug‐resistant bacteria. Citronellol's environmental benignity makes CDs less hemolytic. Notably, negligible drug resistance developed after 15 bacterial subcultures. The CD‐treated cotton fabric displayed better antibacterial performance than AAA‐grade antibacterial fabric, even after repeated washing. This study extends the practical application of EOs to antibacterial surfaces and fabrics, which is promising for use in personal care products and medical settings.
Polymer/inorganic colloidal nanocomposites can be prepared via Pickering emulsion polymerization (PEP); however, this process usually requires the use of surfactants, auxiliary comonomers, and volatile organic compounds. Herein, we report a versatile and efficient method for synthesizing stable monodisperse polymer/silica colloidal nanocomposite particles via PEP. First, silica nanoparticles were modified by depositing a multifunctional polydopamine (PDA) film. The outermost PDA film could enhance the precipitation of oligomeric polymer radicals on the silica surface, which is crucial for the preparation of stable polymer/inorganic colloidal nanocomposites via PEP. Notably, this PDA modification approach can employ different initiator systems, such as cationic initiators and redox initiator couples, and can be applied to various monomers and monomer pairs (St, St/nBA, MMA, MMA/nBA, Vac, Vac/nBA). The influence of the concentration and size of polydopamine-coated silica (SiO2@PDA) on the colloidal nanocomposite was investigated. Increasing the diameter of SiO2@PDA and decreasing the concentration of SiO2@PDA both lead to the formation of larger nanocomposite particles. Considering its wide applicability, the proposed PDA modification approach can be applied to other functional inorganic particles to prepare multifunctional polymer/inorganic nanocomposite particles.
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