通过水插层激活MoO3纳米带作为近红外I型光敏剂用于光动力牙周炎治疗

SmartMat Pub Date : 2023-09-13 DOI:10.1002/smm2.1243
Bohua Li, Dandan Chu, Haohao Cui, Zhanrong Li, Zhan Zhou, Chaoliang Tan, Jingguo Li
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引用次数: 2

摘要

虽然三氧化钼纳米材料已经通过光热疗法、化学动力疗法和催化疗法被广泛探索作为生物医学应用的纳米药物,但它们作为光动力疗法(PDT)的光敏剂的应用迄今为止很少有报道。在这里,我们报道了通过在van der Waals间隙中水溶液共插Na +和h2o活化moo3纳米带作为近红外I型光敏剂用于光动力牙周炎治疗。在moo3纳米带中插入Na + / h2o可以缩短其长度,产生丰富的氧空位,并扩大其层间间隙。因此,这种结构变化可以诱导颜色从白色变为深蓝色,具有很强的近红外吸收。当用作光敏剂时,在808 nm激光照射下,I‐moo3 - x纳米带比原始moo3纳米带具有更高的生成超氧自由基(·o2 -)的活性。因此,制备的I‐MoO 3−x纳米带对大肠杆菌和金黄色酵母菌具有抗菌活性,因此对牙周炎具有良好的临床治疗效果。我们的研究证明,水插层可以是一种简单但强大的策略来激活层状moo3纳米材料,用于高性能PDT。
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Activating MoO3 nanobelts via aqueous intercalation as a near‐infrared type I photosensitizer for photodynamic periodontitis treatment
Abstract Although molybdenum trioxide nanomaterials have been widely explored as nanoagents for biomedical applications against bacteria through photothermal therapy, chemodynamic therapy, and catalytic therapy, their utilization as photosensitizers for photodynamic therapy (PDT) have been rarely reported so far. Herein, we report the activation of MoO 3 nanobelts via aqueous co‐intercalation of Na + and H 2 O into their van der Waals gaps as a near‐infrared Type I photosensitizer for photodynamic periodontitis treatment. The Na + /H 2 O intercalation of MoO 3 nanobelts can shorten its length, generate rich oxygen vacancies, and enlarge its interlayer gaps. Such structural changes thus can induce the color change from white to dark blue with a strong near‐infrared (NIR) absorption. When used as a photosensitizer, the I‐MoO 3− x nanobelts exhibit much higher activities for the generation of superoxide radical (·O 2 − ) under an 808 nm laser irradiation than that of the pristine MoO 3 nanobelts. Therefore, the prepared I‐MoO 3− x nanobelts show a spectral antibacterial activity against Escherichia coli and Saccharomyces aureus , thus yielding a good clinical therapeutic effect on periodontitis. Our study proves that aqueous intercalation can be a simple but powerful strategy to activate layered MoO 3 nanomaterials for high‐performance PDT.
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