Hunwin Kayleigh, Page Georgina, Edgar Mark, Botana Adolfo, Armitage Rachel, Bhogadia Mohammed, Desai Unmesh, Duffin Steven, Duffin Marcus, Chan Wyman, Grootveld Martin
Leicester School of Pharmacy, De Montfort University, The Gateway, Leicester, United Kingdom.
JEOL (U.K.) Ltd., Welwyn Garden City, United Kingdom.
Front Oral Health. 2024 Jul 23;5:1412751. doi: 10.3389/froh.2024.1412751. eCollection 2024.
This paper serves as a Part II follow-up of our research investigations performed on the molecular structures of silver(I)-fluoride (SF) and diammine-silver(I) fluoride (SDF) complexes in solution-based commercial products for clinical application, their precise chemical compositions, and their nature in aqueous solution, the latter including rapid fluoride-exchange processes at the silver(I) ion centre monitored by F NMR analysis (Part I). Part I of this series also explores the mechanisms of action (MoA) of these complexes, and is therefore largely focused on their chemical reactions with constituents of human saliva, which has access to their sites of application. Such reactions were found to slowly promote the generation of potentially physiologically-active Ag/AgCl nanoparticles from primarily-generated discoloured silver(I) chloride (AgCl) precipitates, a process involving salivary electron-donors such as thiocyanate and L-cysteine. Since this research has shed new light on potential MoAs for these products, in this accompanying report (Part II), we have performed a critical review of scientific literature in order to rationalize our results in relation to current views on these mechanisms for SF and SDF products employed for the successful clinical arrest of dental caries. Following an Introduction to the subject matter ( Section 1), this paper comprises a generalized overview of silver coordination chemistry ( Section 2), which is followed by a section focused on the aqueous solution status and equilibria involved in SF chemistry ( Section 3), the latter including results acquired from an original simulation of the electronic absorption spectra of coloured SF complexes in aqueous solution (Section 3.1). Section 4 then investigates detailed rationales for the biologically-relevant ligand-exchange and redox chemistries, disposition and fates of SF, SDF and silver(I)-nitrate when employed for the treatment of dental caries, with emphasis placed on their therapeutic MoAs. This Section is supported by the provision of valuable information centralized on (1) relevant biomolecular chemistry involved in solution- and solid-state matrices ( Section 4.1); (2) SF and perhaps silver(I)-nitrate as more cost-effective alternatives to SDF therapies ( Section 4.2); and (3) the potential therapeutic benefits and effects offered by silver-based nanoparticles and their associated MoAs ( Section 4.3). Recommendations for future investigations in this area are proposed.
本文是我们对临床应用的溶液型商业产品中氟化银(SF)和二氨合氟化银(SDF)配合物的分子结构、精确化学组成及其在水溶液中的性质所进行研究调查的第二部分后续内容,后者包括通过F NMR分析监测的银(I)离子中心的快速氟交换过程(第一部分)。本系列的第一部分还探讨了这些配合物的作用机制(MoA),因此主要关注它们与可接触到其应用部位的人类唾液成分的化学反应。发现此类反应会缓慢促进从最初生成的变色氯化银(AgCl)沉淀物中生成潜在具有生理活性的Ag/AgCl纳米颗粒,这一过程涉及唾液电子供体,如硫氰酸盐和L-半胱氨酸。由于这项研究为这些产品的潜在作用机制带来了新的认识,在这份附带报告(第二部分)中,我们对科学文献进行了批判性综述,以便将我们的结果与目前关于用于成功临床防治龋齿的SF和SDF产品这些机制的观点联系起来进行合理化分析。在对主题进行介绍(第1节)之后,本文包括对银配位化学的一般性概述(第2节),随后是一节重点关注SF化学中涉及的水溶液状态和平衡(第3节),后者包括从对水溶液中有色SF配合物的电子吸收光谱的原始模拟中获得的结果(第3.1节)。然后第4节研究了SF、SDF和硝酸银(I)用于治疗龋齿时与生物学相关的配体交换和氧化还原化学、分布及归宿的详细原理,重点是它们的治疗作用机制。本节得到了以下方面提供的有价值信息的支持:(1)溶液和固态基质中涉及的相关生物分子化学(第4.1节);(2)SF以及或许硝酸银(I)作为比SDF疗法更具成本效益的替代方案(第4.2节);以及(3)银基纳米颗粒及其相关作用机制提供的潜在治疗益处和效果(第4.3节)。并提出了该领域未来研究的建议。