Affiliation:
1. Sorbonne Université CNRS Laboratoire de Réactivité de Surface (LRS) Paris F‐75005 France
2. Laboratoire de Biomécanique & Bioingénierie CNRS Université de Technologie de Compiègne BP 20529 Compiègne Cedex F‐60205 France
3. Service Analyses Physico‐Chimiques SAPC Université de Technologie de Compiègne BP 20529 Compiègne Cedex F‐60205 France
4. Fédération de Chimie et Matériaux de Paris‐Centre (FCMat) FR2482 Paris F‐75005 France
5. Univ Rouen Normandie, INSA Rouen Normandie CNRS Normandie Univ Polymères Biopolymères et Surfaces (PBS, UMR 6270) 55 Rue Saint‐Germain Évreux 27 000 France
Abstract
AbstractBiomimetic hydroxyapatites are widely explored for their potential applications in the repair of mineralized tissues, particularly dental enamel, which is acellular and, thus, not naturally reformed after damage. Enamel is formed with a highly‐controlled hierarchical structure, which is difficult to replicate up to the macroscale. A biomimetic approach is thus warranted, based on the same principles that drive biomineralization in vivo. Herein, a strategy for the design of enamel‐like architectures is described, utilizing enzymes embedded in polyelectrolyte multilayers to generate inorganic phosphate locally, and provide a favorable chemical environment for the nucleation and growth of minerals. Moreover, a method is proposed to build up seriated mineral layers with scalable thicknesses, continuous mineral growth, and tunable morphology. Results show the outstanding growth of cohesive mineral layers, yielding macroscopic standalone fluoride and/or carbonate‐substituted hydroxyapatite materials with comparable crystal structure and composition to native human mineralized tissues. This strategy presents a promising path forward for the biomimetic design of biomineral materials, particularly relevant for restorative applications, with an exquisite level of synthetic control over multiple orders of magnitude.