This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Dendrimers are highly customizable polymers that act as basic building blocks allowing specific nanostructures to be built. The purpose of this project is to design dendrimers that cross the blood brain barrier (BBB), for potential use in drug delivery.
The aims of this project are to synthesize and charaterize novel poly(lysine) dendrimers and poly(amidoamine) (PAMAM) dendrimers, each with a biotin label or dansyl chloride label and surface groups including anandamide (a compound that may aid the dendrimer in crossing the BBB). Additionally, we will investigate dendrimer penetration into model lipid bilayers using attenuated total reflection infrared spectroscopy; characterize the fundamental interactions of dendrimer nanostructures at a solid/solution interface using scanning probe microscopy; measure the passage of dendrimers across a cell co-culture of brain endothelial cells and astrocytes and through the rat BBB, using ultra performance liquid chromatography (UPLC) and HPLC. Collectively, these studies will provide valuable information on the use of dendrimers in applications such as drug delivery and chemical sensing. This far, we have sunthesized all G4 and G5 PAMAM dendrimer conjugates and submitted a manuscript to Journal of Nanomaterials (with undergraduate student co-authors). In the paper, UPLC analysis was utilized for the first time as a methodology for monitoring PAMAM dendrimer surface transformations (biotin) and product quality. Currently, we are testing of passage of various dendrimers across the in vitro BBB model. Faculty Mentor Robert Yokel will share his in vivo method of testing nanoparticle passage across a rat BBB in the next 2 weeks as PI Martines will travel to UK to perfect this technique. An NIH R15 grant proposal and SOMAS (Support of Mentors and their Students in the Neurosciences) grant proposal are currently in review. Two internal grant proposals were awarded. Manuscripts are also in prepar ation for the characteriztion and in vitro and in vivo studies. PI Martines traveled to Magdeburg, Germany to establish a collaboration with the University of Madgeburg Medical School where new nanoparticles (with potential of treating glioma) and a new in vivo model will be shared, trip supported by NKU Research Foundation grant.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR016481-08
Application #
7720148
Study Section
Special Emphasis Panel (ZRR1-RI-7 (01))
Project Start
2008-05-01
Project End
2009-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
8
Fiscal Year
2008
Total Cost
$16,887
Indirect Cost
Name
University of Louisville
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
057588857
City
Louisville
State
KY
Country
United States
Zip Code
40292
Stenslik, M J; Evans, A; Pomerleau, F et al. (2018) Methodology and effects of repeated intranasal delivery of DNSP-11 in awake Rhesus macaques. J Neurosci Methods 303:30-40
Green, Kimberly A; Becker, Yvonne; Fitzsimons, Helen L et al. (2016) An Epichloƫ festucae homologue of MOB3, a component of the STRIPAK complex, is required for the establishment of a mutualistic symbiotic interaction with Lolium perenne. Mol Plant Pathol 17:1480-1492
Rouchka, Eric C; Flight, Robert M; Fasciotto, Brigitte H et al. (2016) Transcriptional profile of immediate response to ionizing radiation exposure. Genom Data 7:82-5
Saikkonen, Kari; Young, Carolyn A; Helander, Marjo et al. (2016) Endophytic Epichloƫ species and their grass hosts: from evolution to applications. Plant Mol Biol 90:665-75
Smith, Michael E; Monroe, J David (2016) Causes and Consequences of Sensory Hair Cell Damage and Recovery in Fishes. Adv Exp Med Biol 877:393-417
Witkowski, Travis A; Grice, Alison N; Stinnett, DeAnna B et al. (2016) UmuDAb: An Error-Prone Polymerase Accessory Homolog Whose N-Terminal Domain Is Required for Repression of DNA Damage Inducible Gene Expression in Acinetobacter baylyi. PLoS One 11:e0152013
Hofmann, Emily; Webster, Jonathan; Do, Thuy et al. (2016) Hydroxylated chalcones with dual properties: Xanthine oxidase inhibitors and radical scavengers. Bioorg Med Chem 24:578-87
Harrison, Benjamin J; Venkat, Gayathri; Lamb, James L et al. (2016) The Adaptor Protein CD2AP Is a Coordinator of Neurotrophin Signaling-Mediated Axon Arbor Plasticity. J Neurosci 36:4259-75
Rau, Kristofer K; Hill, Caitlin E; Harrison, Benjamin J et al. (2016) Cutaneous tissue damage induces long-lasting nociceptive sensitization and regulation of cellular stress- and nerve injury-associated genes in sensory neurons. Exp Neurol 283:413-27
Gemmell, Amber P; Marcus, Jeffrey M (2015) A tale of two haplotype groups: Evaluating the New World Junonia ring species hypothesis using the distribution of divergent COI haplotypes. Syst Entomol 40:532-546

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