Materiomics using synthetic materials: Metals, cements, covalent polymers and supramolecular systems

Björne B. Mollet, A.C.H. Pape, Rosa P. Félix Lanao, Sander C.G. Leeuwenburgh, Patricia Y.W. Dankers

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To screen biomaterials in a materiomics approach, libraries of materials are produced. Different materials are used, varying from metals and cements, to covalent polymers that can be either premixed or polymerized in situ, to supramolecular systems that can be applied in a modular approach. This chapter describes the generation of such libraries using different kinds of materials and chemistries. Additionally, the advantages and limitations of the application of these different systems/biomaterials in a materiomics approach are discussed. Different synthetic biomaterials are used for many biomedical applications, varying from metals and ceramic cements, to polymers and supramolecular systems. To screen these biomaterials in a materiomics approach, as said above, libraries of materials are produced. Variations in biomaterials are screened as continuous gradients or in a discrete fashion. The properties that are varied and methods used to create variation within these libraries depend on the type of biomaterial. For the hard metal and ceramic-based biomaterials, the surface interaction with tissue is the property of most interest, and therefore properties such as surface roughness and topography are varied. Covalent polymers are diversified using combinatorial chemistry. The dynamic and self-assembling nature of supramolecular systems allows for the development of material libraries using a modular approach by mixing and matching of different compounds modified with supramolecular moieties.

Original languageEnglish
Title of host publicationMateriomics
Subtitle of host publicationHigh-Throughput Screening of Biomaterial Properties
EditorsJan de Boer, Clemens A. van Blitterswijk
PublisherCambridge University Press
Number of pages20
ISBN (Electronic)9781139061414
ISBN (Print)9781107016774
Publication statusPublished - 1 Jan 2011


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