0000000000433750

AUTHOR

Matthew J. Webber

0000-0003-3111-6228

showing 5 related works from this author

Dynamic In Vivo Biocompatibility of Angiogenic Peptide Amphiphile Nanofibers

2009

Biomaterials that promote angiogenesis have great potential in regenerative medicine for rapid revascularization of damaged tissue, survival of transplanted cells, and healing of chronic wounds. Supramolecular nanofibers formed by self-assembly of a heparin-binding peptide amphiphile and heparan sulfate-like glycosaminoglycans were evaluated here using a dorsal skinfold chamber model to dynamically monitor the interaction between the nanofiber gel and the microcirculation, representing a novel application of this model. We paired this model with a conventional subcutaneous implantation model for static histological assessment of the interactions between the gel and host tissue. In the stati…

Materials scienceBiocompatibilityAngiogenesisBiophysicsConnective tissueBioengineeringBiocompatible Materials02 engineering and technology010402 general chemistry01 natural sciencesRegenerative medicineArticleMicrocirculationBiomaterialsMiceImplants ExperimentalFluorescence microscopemedicinePeptide amphiphileAnimalsAngiogenic ProteinsMicrocirculation021001 nanoscience & nanotechnology0104 chemical sciences3. Good healthmedicine.anatomical_structureMicroscopy FluorescenceMechanics of MaterialsNanofiberCeramics and CompositesFemaleHeparitin Sulfate0210 nano-technologyBiomedical engineering
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Scaffold vascularization in vivo driven by primary human osteoblasts in concert with host inflammatory cells.

2011

Successful cell-based tissue engineering requires a rapid and thorough vascularization in order to ensure long-term implant survival and tissue integration. The vascularization of a scaffold is a complex process, and is modulated by the presence of transplanted cells, exogenous and endogenous signaling proteins, and the host tissue reaction, among other influencing factors. This paper presents evidence for the significance of pre-seeded osteoblasts for the in vivo vascularization of a biodegradable scaffold. Human osteoblasts, cultured on silk fibroin micronets in vitro, migrated throughout the interconnected pores of the scaffold and produced extensive bone matrix. When these constructs we…

Vascular Endothelial Growth Factor AScaffoldMaterials scienceTime FactorsAngiogenesisCellBiophysicsFibroinNeovascularization PhysiologicBioengineeringMice SCIDBiomaterialsProsthesis ImplantationMiceTissue engineeringIn vivomedicineAnimalsHumansCells CulturedInflammationOsteoblastsTissue ScaffoldsIn vitroCell biologymedicine.anatomical_structureMechanics of MaterialsGiant cellCeramics and CompositesBlood VesselsFibroinsBiomedical engineeringBiomaterials
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Evaluation of the tissue reaction to a new bilayered collagen matrix in vivo and its translation to the clinic.

2011

This study evaluates a new collagen matrix that is designed with a bilayered structure in order to promote guided tissue regeneration and integration within the host tissue. This material induced a mild tissue reaction when assessed in a murine model and was well integrated within the host tissue, persisting in the implantation bed throughout the in vivo study. A more porous layer was rapidly infiltrated by host mesenchymal cells, while a layer designed to be a barrier allowed cell attachment and host tissue integration, but at the same time remained impermeable to invading cells for the first 30 days of the study. The tissue reaction was favorable, and unlike a typical foreign body respons…

MaleMaterials scienceBiomedical EngineeringConnective tissueNeovascularization PhysiologicBioengineeringContext (language use)Pilot ProjectsMatrix (biology)BiomaterialsMiceMaterials TestingmedicineAnimalsHumansTissue ScaffoldsRegeneration (biology)Foreign-Body ReactionMesenchymal stem cellGranulation tissueSoft tissueBiomaterialCell biologymedicine.anatomical_structureGuided Tissue Regeneration PeriodontalMicroscopy Electron ScanningFemaleCollagenPorosityBiomedical engineeringBiomedical materials (Bristol, England)
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Rapid vascularization of starchâ poly(caprolactone) in vivo by outgrowth endothelial cells in co-culture with primary osteoblasts

2011

The successful integration of in vitro-generated tissues is dependent on adequate vascularization in vivo. Human outgrowth endothelial cells (OECs) isolated from the mononuclear cell fraction of peripheral blood represent a potent population of circulating endothelial progenitors that could provide a cell source for rapid anastomosis and scaffold vascularization. Our previous work with these cells in co-culture with primary human osteoblasts has demonstrated their potential to form perfused vascular structures within a starch–poly(caprolactone) biomaterial in vivo. In the present study, we demonstrate the ability of OECs to form perfused vascular structures as early as 48 h following subcut…

AngiogenesisPolyestersPopulationBiomedical EngineeringNeovascularization PhysiologicMedicine (miscellaneous)02 engineering and technologyBiologyBiomaterialsNeovascularization03 medical and health sciencesTissue engineeringIn vivoIn vivomedicineHumansVimentinProgenitor celleducationCells CulturedCell Proliferation030304 developmental biologyPericyte0303 health scienceseducation.field_of_studyOsteoblastsScience & TechnologyOsteoblastEndothelial CellsOutgrowth endothelial cellStarchOsteoblast021001 nanoscience & nanotechnologyImmunohistochemistryCoculture Techniques3. Good healthCell biologyPlatelet Endothelial Cell Adhesion Molecule-1medicine.anatomical_structureBlood VesselsPericyteAngiogenesismedicine.symptomCo-culture0210 nano-technologyBiomedical engineering
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Fine-tuning scaffolds for tissue regeneration: effects of formic acid processing on tissue reaction to silk fibroin

2010

Formic acid (FA) plays a key role in the preparation of silk fibroin (SF) scaffolds from cocoons of Bombyx mori and is used for fibre distribution. In this study, we used a subcutaneous implantation model in Wistar rats to examine SF scaffolds prepared by treating the degummed cocoon with FA for either 30 or 60 min. The tissue reaction and inflammatory response to SF was assessed by qualitative histology at intervals from 3 to 180 days. Additionally, dynamic biomaterial-induced vascularization and biomaterial degradation were quantified using a technique for analysing an image of the entire implanted biomaterial. Varying the FA treatment time led to different scaffold morphologies and resul…

ScaffoldTime FactorsFormatesBiocompatibilityBiomedical EngineeringNeovascularization PhysiologicMedicine (miscellaneous)FibroinConnective tissueRegenerative MedicineRegenerative medicineBiomaterialsTissue engineeringmedicineAnimalsRegenerationRats WistarStaining and LabelingTissue EngineeringTissue ScaffoldsChemistryBiomaterialHistologyRatsmedicine.anatomical_structureMicroscopy Electron ScanningFibroinsBiomedical engineeringJournal of Tissue Engineering and Regenerative Medicine
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