grant

Personalized Strategies for Periodontal Tissue Regeneration - A Converged Biofabrication Approach

Organization UNIVERSITY OF MICHIGAN AT ANN ARBORLocation ANN ARBOR, UNITED STATESPosted 1 Aug 2022Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY20263-D3-Dimensional3D65 and older65 or older65 years of age and older65 years of age or more65 years of age or older65+ years65+ years oldAddressAdoptedAffectAg elementAged 65 and OverAlveolodental LigamentAlveolodental MembraneAmericanAnimal ModelAnimal Models and Related StudiesArchitectureBacteriaBiocompatible MaterialsBiological FunctionBiological ProcessBiomaterialsBody TissuesBone GrowthCementumCeramicsChemicalsChronicChronic PeriodontitisClinicalDataDefectDental CementumDentitionDevelopmentEngineeringEngineering / ArchitectureFiberGenesGoalsGrowth and DevelopmentGrowth and Development functionGum DiseaseIn VitroInflammatoryInkLaser ElectromagneticLaser RadiationLasersLeftMagnesiumMechanicsMedicineMg elementMorphologyMouth DiseasesNanostructuresNatural regenerationNatureOral Cavity DiseaseOral Cavity DisorderOral DiseaseOral DisorderParodontosisPatientsPeriodontal DiseasesPeriodontal LigamentPeriodontal MembranePeriodonticPeriodontic specialtyPeriodonticsPeriodontitisPhosphatesPhysiologicPhysiologicalPolymersPrintingRegenerationRoleSilverStructureSurfaceTechnologyTherapeuticTissuesTooth ExtractionTooth LossTracheobronchomalaciaTranslatingTranslationsabove age 65after age 65age 65 and greaterage 65 and olderage 65 or olderageage of 65 years onwardaged 65 and greateraged 65+aged ≥65alveolar bonealveolar supporting boneanti-microbialantimicrobialbio-fabricationbiofabricationbiological materialbonebone engineeringbone lossbone scaffoldcalcium phosphate coatingcanine animal modelcanine modelclinical efficacyclinical relevanceclinically relevantdesigndesigningdetermine efficacydevelopmentaldog modelefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationevaluate efficacyexamine efficacyfabricationhuman old age (65+)improvedin vivoin vivo Modelindividualized strategiesinnovateinnovationinnovativeinorganic phosphatemanufacturemaxilla alveolar processmechanicmechanicalmeltingmodel of animalmouth disordernano-sized structuresnano-structuresnovelover 65 yearsperiodontal disorderperiodontium diseaseperiodontium disorderpersonalization of treatmentpersonalized medicinepersonalized strategiespersonalized therapypersonalized treatmentpolymerpolymericregenerateregenerate new tissueregenerate tissueregenerating damaged tissueregenerating tissueregeneration based therapyregeneration therapyregenerative therapeuticsregenerative therapyscaffoldscaffoldingsocial rolesocket wallthree dimensionaltissue regenerationtissue regrowthtissue renewaltissue specific regenerationtooltranslation≥65 years
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Full Description


Periodontitis (gum disease) is a ubiquitous chronic inflammatory, bacteria-triggered oral disorder affecting two-thirds of Americans over age 65. If left untreated, it leads to severe destruction of the periodontal attachment apparatus, eventually resulting in tooth loss. There are no approaches for predictably regenerating defects with severe bone loss and avoiding tooth extraction. Thus, there is an emerging quest for personalized solutions that can guide coordinated growth and development of the periodontal attachment apparatus. We hypothesize that: (1) Melt ElectroWriting (MEW) is the fabrication tool required to develop a compositionally and structurally tailored, tissue-specific scaffold to hearten bone growth and PDL formation on root surfaces with moderate adjacent bone; and (2) the convergence of MEW with ceramic printing is key to engineering a compositionally graded and structurally tailored scaffold to support bone growth while guiding PDL formation on root surfaces with minimum adjacent bone. Two aims are proposed. Aim 1 will optimize a personalized, compositionally and structurally tailored, tissue-specific polymeric scaffold to regenerate defects with moderate surrounding bone. Aim 2 will develop a personalized, compositionally graded and structurally tailored, tissue-specific multi-material scaffold to regenerate defects with minimum surrounding bone. To expedite translation, we will determine efficacy using our clinically relevant animal models. Successful completion of this project is central to translating personalized therapies to treat tissue destruction caused by periodontitis and thus saving millions of teeth from extraction.

Grant Number: 5R01DE031476-05
NIH Institute/Center: NIH

Principal Investigator: Marco Bottino

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