非化学计量FeS2纳米颗粒作为光热和光动力复合抗菌药物的研究

IF 4.7 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-05-01 Epub Date: 2025-01-02 DOI:10.1016/j.jphotochem.2024.116260
Ahmed AlSarori , Abdurrahman Mustafa , Hasan Akyıldız , Ismail Cihan Kaya , Gulcihan Guzel Kaya
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引用次数: 0

摘要

本研究采用热注射法合成了非化学计量的FeS2纳米颗粒,并对其作为双效抗菌剂进行了评价。通过改变前驱体(即铁源和s源)的摩尔比,获得了非化学计量的FeS2纳米颗粒。x射线光电子能谱(XPS)分析表明,当Fe源与S源的比值分别为1/6、1/8、1/10和1/12时,FeS2纳米颗粒中的Fe/S比值分别为1.012:2、0.960:2、0.905:2和0.900:2。在Fe/S: 0.900:2的情况下,808 nm近红外(NIR)光照射下,除了产生活性氧(ROS)外,温度升高到约53℃(光热转换效率为52.6%)。基于体外抗菌活性测试,非化学计量FeS2纳米颗粒由于ROS形成和高温的协同作用,对大肠杆菌(98.00%)和金黄色葡萄球菌(99.89%)表现出良好的抗菌活性。在近红外辐射下,非化学计量FeS2纳米颗粒可以被认为是高潜力的抗菌材料。
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Non-Stoichiometric FeS2 nanoparticles as antibacterial agents with combined photothermal and photodynamic effect
In this study, non-stoichiometric FeS2 nanoparticles were synthesized via hot-injection method and evaluated as dual effect antibacterial agent. Non-stoichiometric FeS2 nanoparticles were achieved by altering the molar ratio of the precursors (i.e., Fe-source and S-source). X-ray photoelectron spectroscopy (XPS) analysis revealed that Fe/S ratio in the FeS2 nanoparticles were 1.012:2, 0.960:2, 0.905:2, and 0.900:2 for the samples with Fe-source to S-source ratios of 1/6, 1/8, 1/10, and 1/12, respectively. In the case of Fe/S: 0.900:2, the temperature increased up to about 53 °C (photothermal conversion efficiency: 52.6 %) in addition to reactive oxygen species (ROS) generation under 808 nm near-infrared (NIR) light irradiation. Based on the in vitro antibacterial activity tests, non-stoichiometric FeS2 nanoparticles exhibited promising antibacterial activity against Escherichia coli (98.00%) and Staphylococcus aureus (99.89%) due to the synergistic effects of ROS formation and hyperthermia. The non-stoichiometric FeS2 nanoparticles can be considered as high potential antibacterial material under NIR irradiation.
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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