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Integrating Image-Based Design and 3D Biomaterial Printing to Create Patient Specific Devices within a Design Control Framework for Clinical Translation

dc.contributor.authorHollister, SJ
dc.contributor.authorFlanagan, CL
dc.contributor.authorMorrison, RJ
dc.contributor.authorPatel, JJ
dc.contributor.authorWheeler, MB
dc.contributor.authorEdwards, SP
dc.contributor.authorGreen, GE
dc.coverage.spatialUnited States
dc.date.accessioned2024-01-09T16:59:02Z
dc.date.available2024-01-09T16:59:02Z
dc.date.issued2016-10-10
dc.identifier.issn2373-9878
dc.identifier.issn2373-9878
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/31231678
dc.identifier.urihttps://hdl.handle.net/2027.42/191956en
dc.description.abstractDespite significant advances in 3D biomaterial printing, the potential of 3D printing for patient specific implants and tissue reconstruction has not been fully exploited. This is due in part to the lack of integration of image-based patient specific design with 3D biomaterial printing within a relevant regulatory framework, namely design control, required by the FDA. In this manuscript, we describe the integration of image-based, multiscale patient specific design with 3D biomaterial printing within a design control framework for clinical translation. Specifically, we define design inputs for patient specific implants and scaffolds, and utilize image-based patient specific design to achieve these design inputs. We then illustrate realization of these topology designed patient specific implants by laser sintering of polycaprolactone (PCL). Finally, we present initial results in large animal models using 3D printed PCL implants addressing two challenging problems in tissue reconstruction: 1) designing and 3D printing implantable devices to allow growth in pediatric airway applications and 2) utilizing 3D printed scaffolds as foundations for prefabricated flaps to obtain vascularization and bone formation for large volume bone/soft tissue reconstruction. We illustrate these challenging problems as they need to be incorporated in design control, but as of yet there are few data to direct how growth and vascularization should be utilized in design control.
dc.format.mediumPrint-Electronic
dc.languageeng
dc.publisherAmerican Chemical Society (ACS)
dc.subject3D Printing
dc.subjectAirway Splint
dc.subjectClinical Translation
dc.subjectDesign Control
dc.subjectImage-Based Design
dc.subjectPatient Specific Implants
dc.subjectPrefabricated Flap
dc.titleIntegrating Image-Based Design and 3D Biomaterial Printing to Create Patient Specific Devices within a Design Control Framework for Clinical Translation
dc.typeArticle
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/191956/2/2016_ACS Biomater_3D Printing Design Control.pdf
dc.identifier.doi10.1021/acsbiomaterials.6b00332
dc.identifier.doihttps://dx.doi.org/10.7302/21957
dc.identifier.sourceACS Biomaterials Science and Engineering
dc.description.versionPublished version
dc.date.updated2024-01-09T16:59:00Z
dc.identifier.orcid0000-0002-2313-8542
dc.identifier.orcid0000-0002-5156-9542
dc.identifier.volume2
dc.identifier.issue10
dc.identifier.startpage1827
dc.identifier.endpage1836
dc.identifier.name-orcidHollister, SJ
dc.identifier.name-orcidFlanagan, CL
dc.identifier.name-orcidMorrison, RJ; 0000-0002-2313-8542
dc.identifier.name-orcidPatel, JJ
dc.identifier.name-orcidWheeler, MB
dc.identifier.name-orcidEdwards, SP
dc.identifier.name-orcidGreen, GE; 0000-0002-5156-9542
dc.working.doi10.7302/21957en
dc.owningcollnameBiomedical Engineering, Department of


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