Dai Lin, Liu Yan, Salameh Ziad, Khan Sara, Mao Jing, Pashley David H, Tay Franklin R
Department of Stomatology, The First Hospital of Wuhan, Wuhan, China.
Dent Hypotheses. 2011 Jan 1;2(2):74-82. doi: 10.5436/j.dehy.2010.1.00011.
To date, there is no evidence that conventional remineralization techniques using calcium and phosphate ion- containing media will completely remineralize carious lesions in regions where remnant apatite seed crystallites are absent. Conversely, guided tissue remineralization using biomimetic analogs of dentin matrix proteins is successful in remineralizing thin layers of completely demineralized dentin. THE HYPOTHESIS: Conventional remineralization strategy depends on epitaxial growth over existing apatite crystallites. If there are no or few crystallites, there will be no remineralization. Guided tissue remineralization uses biomimetic analogs of dentin matrix proteins to introduce sequestered amorphous calcium phosphate nanoprecursors into the internal water compartments of collagen fibrils. Attachment of templating analogs of matrix phosphoproteins to the collagen fibrils further guided the nucleation and growth of apatite crystallites within the fibril. Such a strategy is independent of apatite seed crystallites. Our hypothesis is that 250-300 microns thick artificial carious lesions can be completely remineralized in vitro by guide tissue remineralization but not by conventional remineralization techniques. EVALUATION OF THE HYPOTHESIS: Validation of the hypothesis will address the critical barrier to progress in remineralization of caries- affected dentin and shift existing paradigms by providing a novel method of remineralization based on a nanotechnology-based bottom-up approach. This will also generate important information to support the translation of the proof-of-concept biomimetic strategy into a clinically-relevant delivery system for remineralizing caries-affected dentin created by micro-organisms in the oral cavity.
迄今为止,尚无证据表明使用含钙和磷酸根离子介质的传统再矿化技术能使不存在残余磷灰石籽晶微晶的区域的龋损完全再矿化。相反,使用牙本质基质蛋白的仿生类似物进行引导组织再矿化能成功使完全脱矿的牙本质薄层再矿化。
传统再矿化策略依赖于在现有磷灰石微晶上的外延生长。如果没有或只有很少的微晶,就不会有再矿化。引导组织再矿化使用牙本质基质蛋白的仿生类似物将螯合的无定形磷酸钙纳米前体引入胶原纤维的内部水腔。基质磷蛋白的模板类似物附着在胶原纤维上进一步引导了纤维内磷灰石微晶的成核和生长。这样的策略独立于磷灰石籽晶微晶。我们的假设是,250 - 300微米厚的人工龋损在体外可通过引导组织再矿化完全再矿化,但不能通过传统再矿化技术实现。
对该假设的验证将解决龋损牙本质再矿化进展中的关键障碍,并通过提供一种基于纳米技术的自下而上方法的新型再矿化方法来改变现有范式。这也将产生重要信息,以支持将概念验证仿生策略转化为用于再矿化口腔中微生物造成的龋损牙本质的临床相关递送系统。