Huang Yue, Liu Yuan, Pandey Nil, Shah Shrey, Simon-Soro Aurea, Hsu Jessica, Ren Zhi, Xiang Zhenting, Kim Dongyeop, Ito Tatsuro, Oh Min Jun, Buckley Christine, Alawi Faizan, Li Yong, Smeets Paul, Boyer Sarah, Zhao Xingchen, Joester Derk, Zero Domenick, Cormode David, Koo Hyun
University of Pennsylvania.
Biofilm Research Labs, Levy Center for Oral Health, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Res Sq. 2023 Apr 3:rs.3.rs-2723097. doi: 10.21203/rs.3.rs-2723097/v1.
Dental caries (tooth decay) is the most prevalent human disease caused by oral biofilms, affecting nearly half of the global population despite increased use of fluoride, the mainstay anticaries (tooth-enamel protective) agent. Recently, an FDA-approved iron oxide nanozyme formulation (ferumoxytol, Fer) has been shown to disrupt caries-causing biofilms with high specificity via catalytic activation of hydrogen peroxide, but it is incapable of interfering with enamel acid demineralization. Here, we find notable synergy when Fer is combined with stannous fluoride (SnF ), markedly inhibiting both biofilm accumulation and enamel damage more effectively than either alone. Unexpectedly, our data show that SnF enhances the catalytic activity of Fer, significantly increasing reactive oxygen species (ROS) generation and antibiofilm activity. We discover that the stability of SnF (unstable in water) is markedly enhanced when mixed with Fer in aqueous solutions without any additives. Further analyses reveal that Sn is bound by carboxylate groups in the carboxymethyl-dextran coating of Fer, thus stabilizing SnF and boosting the catalytic activity. Notably, Fer in combination with SnF is exceptionally effective in controlling dental caries , preventing enamel demineralization and cavitation altogether without adverse effects on the host tissues or causing changes in the oral microbiome diversity. The efficacy of SnF is also enhanced when combined with Fer, showing comparable therapeutic effects at four times lower fluoride concentration. Enamel ultrastructure examination shows that fluoride, iron, and tin are detected in the outer layers of the enamel forming a polyion-rich film, indicating co-delivery onto the tooth surface. Overall, our results reveal a unique therapeutic synergism using approved agents that target complementary biological and physicochemical traits, while providing facile SnF stabilization, to prevent a widespread oral disease more effectively with reduced fluoride exposure.
龋齿(蛀牙)是由口腔生物膜引起的最普遍的人类疾病,尽管作为主要防龋(保护牙釉质)剂的氟化物使用有所增加,但仍影响着近一半的全球人口。最近,一种经美国食品药品监督管理局(FDA)批准的氧化铁纳米酶制剂( ferumoxytol,Fer)已被证明可通过过氧化氢的催化活化以高特异性破坏致龋生物膜,但它无法干扰牙釉质酸脱矿。在此,我们发现Fer与氟化亚锡(SnF₂)联合使用时具有显著的协同作用,比单独使用任何一种更有效地显著抑制生物膜积累和牙釉质损伤。出乎意料的是,我们的数据表明SnF₂增强了Fer的催化活性,显著增加了活性氧(ROS)的产生和抗生物膜活性。我们发现,在没有任何添加剂的水溶液中,SnF₂与Fer混合时,其稳定性(在水中不稳定)显著增强。进一步分析表明,Sn²⁺与Fer的羧甲基葡聚糖涂层中的羧基结合,从而稳定了SnF₂并提高了催化活性。值得注意的是,Fer与SnF₂联合使用在控制龋齿方面异常有效,完全防止牙釉质脱矿和空洞形成,而对宿主组织没有不良影响,也不会导致口腔微生物群多样性的变化。SnF₂与Fer联合使用时其功效也得到增强,在氟化物浓度降低四倍时显示出相当的治疗效果。牙釉质超微结构检查表明,在牙釉质外层检测到氟、铁和锡,形成了富含聚离子的膜,表明它们共同递送至牙齿表面。总体而言,我们的结果揭示了一种独特的治疗协同作用,使用经批准的针对互补生物学和物理化学特性的药物,同时提供简便的SnF₂稳定化,以更有效地预防一种广泛的口腔疾病,同时减少氟暴露。