The morphological characteristics and the mechanical properties of advanced biomaterials are the determining factors for their successful applications in drug delivery and tissue engineering applications. In drug delivery, the morphology and the mechanical properties of synthetic biomaterials determine the tissue distribution and the ultimate fate of the drug carriers. Depending on the shape, size and porosity of polymeric particles, the kinetics and the mechanisms of cellular internationalization can be dramatically different. In the context of tissue engineering, the structures of scaffolding materials, from the molecular level to the macroscopic scale, determine the mechanical properties, solute diffusion and cell-matrix interactions. Indeed, Nature modulates the mechanical properties of biological tissues by subtle adjustments of its composition with a perceivable alteration of its nanoscale organization. Recent studies have confirmed the effects of matrix stiffness in controlling cell morphology, adhesion, proliferation and differentiation. An interesting new development in recent years is the alteration of materials structures in response to the applied chemical signals and mechanical stress and how these stimuli can be used to manipulate the spatial distribution of biological signals. The Microscopy and Mechanical Testing (MMT) Core, equipped with stateof- the-art imaging techniques, scattering tools and mechanical testing capabilities, is designed to answer these important questions. The MMT Core was established during previous COBRE funding years and will be strengthened and maintained by our COBRE team through new method developments. The MMT Core will be developed in two steps. The initial phase (years 1-3) focuses on cultivating user groups, facility development and staff training, leading to the mature phase (years 4-5 & beyond) where the Core will be self- sustained with user-fees.

Public Health Relevance

The ability to develop advanced biomaterials with customized control over morphological, mechanical and biological properties will lead to significant advancement in biomedical fields. The MMT Core will provide advanced characterization capabilities to help COBRE researchers gain fundamental understanding of structure-property relationship of their materials in the context of specific cellular and tissue environment. These studies will ultimately generate materials systems that are optimized for their targeted drug delivery and tissue engineering applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
5P30GM110758-03
Application #
9117577
Study Section
Special Emphasis Panel (ZGM1-TWD-C)
Project Start
Project End
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
3
Fiscal Year
2016
Total Cost
$63,743
Indirect Cost
$22,882
Name
University of Delaware
Department
Type
DUNS #
059007500
City
Newark
State
DE
Country
United States
Zip Code
19716
He, Chuan; Teplyakov, Andrew V (2018) 29,31- H Phthalocyanine Covalently Bonded Directly to a Si(111) Surface Retains Its Metalation Ability. Langmuir 34:10880-10888
Dick, Robert A; Zadrozny, Kaneil K; Xu, Chaoyi et al. (2018) Inositol phosphates are assembly co-factors for HIV-1. Nature 560:509-512
Macdougall, Laura J; Wiley, Katherine L; Kloxin, April M et al. (2018) Design of synthetic extracellular matrices for probing breast cancer cell growth using robust cyctocompatible nucleophilic thiol-yne addition chemistry. Biomaterials 178:435-447
Drolen, Claire; Conklin, Eric; Hetterich, Stephen J et al. (2018) pH-Driven Mechanistic Switching from Electron Transfer to Energy Transfer between [Ru(bpy)3]2+ and Ferrocene Derivatives. J Am Chem Soc 140:10169-10178
Dicker, K T; Song, J; Moore, A C et al. (2018) Core-shell patterning of synthetic hydrogels via interfacial bioorthogonal chemistry for spatial control of stem cell behavior. Chem Sci 9:5394-5404
Sawicki, Lisa A; Choe, Leila H; Wiley, Katherine L et al. (2018) Isolation and Identification of Proteins Secreted by Cells Cultured within Synthetic Hydrogel-Based Matrices. ACS Biomater Sci Eng 4:836-845
Duan, Yichen; Rani, Sana; Newberg, John T et al. (2018) Investigation of the influence of oxygen plasma on supported silver nanoparticles. J Vac Sci Technol A 36:01B101
Sallam, Sahar; Dolog, Ivan; Paik, Bradford A et al. (2018) Sequence and Conformational Analysis of Peptide-Polymer Bioconjugates by Multidimensional Mass Spectrometry. Biomacromolecules 19:1498-1507
Wang, Mingzhang; Lu, Manman; Fritz, Matthew P et al. (2018) Fast Magic-Angle Spinning 19 F?NMR Spectroscopy of HIV-1 Capsid Protein Assemblies. Angew Chem Int Ed Engl 57:16375-16379
Sutherland, Bryan P; El-Zaatari, Bassil M; Halaszynski, Nicole I et al. (2018) On-Resin Macrocyclization of Peptides Using Vinyl Sulfonamides as a Thiol-Michael ""Click"" Acceptor. Bioconjug Chem :

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