Department of Preventive & Restorative Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.
Biofilm Research Laboratories, Levy Center for Oral Health, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.
Nano Lett. 2021 Nov 24;21(22):9442-9449. doi: 10.1021/acs.nanolett.1c02702. Epub 2021 Oct 25.
Severe tooth decay has been associated with iron deficiency anemia that disproportionally burdens susceptible populations. Current modalities are insufficient in severe cases where pathogenic dental biofilms rapidly accumulate, requiring new antibiofilm approaches. Here, we show that ferumoxytol, a Food and Drug Administration-approved nanoparticle formulation for treating iron deficiency, exerts an alternative therapeutic activity via the catalytic activation of hydrogen peroxide, which targets bacterial pathogens in biofilms and suppresses tooth enamel decay in an intraoral human disease model. Data reveal the potent antimicrobial specificity of ferumoxytol iron oxide nanoparticles (FerIONP) against biofilms harboring via preferential binding that promotes bacterial killing through free-radical generation. Further analysis indicates that the targeting mechanism involves interactions of FerIONP with pathogen-specific glucan-binding proteins, which have a minimal effect on commensal streptococci. In addition, we demonstrate that FerIONP can detect pathogenic biofilms on natural teeth via a facile colorimetric reaction. Our findings provide clinical evidence and the theranostic potential of catalytic nanoparticles as a targeted anti-infective nanomedicine.
严重的龋齿与缺铁性贫血有关,而缺铁性贫血不成比例地给易感人群带来负担。目前的方法在致病牙菌斑迅速积累的严重情况下是不够的,需要新的抗生物膜方法。在这里,我们表明,铁氧体,一种用于治疗缺铁的美国食品和药物管理局批准的纳米颗粒制剂,通过过氧化氢的催化激活发挥替代治疗活性,靶向生物膜中的细菌病原体,并抑制口腔内人类疾病模型中的牙釉质衰变。数据显示,铁氧体纳米颗粒(FerIONP)对携带的生物膜具有很强的抗菌特异性 通过优先结合促进细菌杀伤的自由基生成。进一步的分析表明,靶向机制涉及 FerIONP 与病原体特异性葡聚糖结合蛋白的相互作用,这对共生链球菌的影响很小。此外,我们证明 FerIONP 可以通过简单的比色反应检测天然牙齿上的致病生物膜。我们的发现为催化纳米颗粒作为靶向抗感染纳米药物提供了临床证据和治疗潜力。
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