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 #
1P30GM110758-01
Application #
8735401
Study Section
Special Emphasis Panel (ZGM1-TWD-C (C3))
Project Start
Project End
Budget Start
2014-09-30
Budget End
2015-07-31
Support Year
1
Fiscal Year
2014
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
Smith, Natalee J; Rohlfing, Katarina; Sawicki, Lisa A et al. (2018) Fast, irreversible modification of cysteines through strain releasing conjugate additions of cyclopropenyl ketones. Org Biomol Chem 16:2164-2169
Zhao, Jing; Konh, Mahsa; Teplyakov, Andrew (2018) Surface Chemistry of Thermal Dry Etching of Cobalt Thin Films Using Hexafluoroacetylacetone (hfacH). Appl Surf Sci 455:438-445
Garcia Garcia, Cristobal; Kiick, Kristi L (2018) Methods for producing microstructured hydrogels for targeted applications in biology. Acta Biomater :
Paramasivam, Sivakumar; Gronenborn, Angela M; Polenova, Tatyana (2018) Backbone amide 15N chemical shift tensors report on hydrogen bonding interactions in proteins: A magic angle spinning NMR study. Solid State Nucl Magn Reson 92:1-6
Wu, Pengcheng; Yap, Glenn P A; Theopold, Klaus H (2018) Structure and Reactivity of Chromium(VI) Alkylidenes. J Am Chem Soc 140:7088-7091
Fritz, Matthew; Quinn, Caitlin M; Wang, Mingzhang et al. (2018) Determination of accurate backbone chemical shift tensors in microcrystalline proteins by integrating MAS NMR and QM/MM. Phys Chem Chem Phys 20:9543-9553
Gupta, Rupal; Stringer, John; Struppe, Jochem et al. (2018) Direct detection and characterization of bioinorganic peroxo moieties in a vanadium complex by 17O solid-state NMR and density functional theory. Solid State Nucl Magn Reson 91:15-20
Liu, Jun; Chen, Qingqing; Rozovsky, Sharon (2018) Selenocysteine-Mediated Expressed Protein Ligation of SELENOM. Methods Mol Biol 1661:265-283
O'Brien, Jessica G K; Chintala, Srinivasa R; Fox, Joseph M (2018) Stereoselective Synthesis of Bicyclo[6.1.0]nonene Precursors of the Bioorthogonal Reagents s-TCO and BCN. J Org Chem 83:7500-7503
Burch, Jason M; Mashayekh, Siavash; Wykoff, Dennis D et al. (2018) Bacterial Derived Carbohydrates Bind Cyr1 and Trigger Hyphal Growth in Candida albicans. ACS Infect Dis 4:53-58

Showing the most recent 10 out of 177 publications