The application of nanotechnology to drug transport requires an understanding of how nanoscale materials interact with and cross cellular membranes. The principle mechanisms debated in the literature for internalization of nanoscale materials into cells include energy-dependent endocytosis, energy-independent membrane translocation, and energy-dependent formation of nanoscale membrane holes. This research program will test these three mechanistic hypotheses for an important class of nanoscale materials, dendrimers, amine-terminated polycationic polymers, and cell-penetrating peptides, that have relevance to drug delivery and cell transfection. In addition to assessing the relative significance of these three internalization mechanisms, the research program will also explore the key physical interactions between the nanoscale materials and the membrane that cause cell membrane permeability. This is important regardless of the mechanism used for internalization since induction of permeability could lead to poor selectivity in drug delivery applications and/or toxicity. Developing an understanding of the physical parameters that lead to cell membrane permeability, and exploring the possible formation of nanoscale membrane holes as a microscopic mechanism of permeabiliy, is important for the rational use of nanotechnology for the application of drug transport.
The specific aims of this research are: 1) assessment of the membrane interaction and transport mechanism of a class of nanoscale materials including dendrimers and polycationic polymers 2) quantification of the relationship between hole formation in lipid bilayers and the size, surface chemistry, and charge of the nanoscale materials 3) determination of the extent and nature of nanoscale hole formation in living cell membranes induced by the nanoscale materials. This work is relevant to public health because it will provide the basic understanding needed to design delivery platforms for drug or gene therapy. Properly designed systems will lead to therapeutics with signficantly reduced side effects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB005028-04
Application #
7640879
Study Section
Biomaterials and Biointerfaces Study Section (BMBI)
Program Officer
Henderson, Lori
Project Start
2006-09-15
Project End
2010-08-14
Budget Start
2009-07-01
Budget End
2010-08-14
Support Year
4
Fiscal Year
2009
Total Cost
$276,170
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Merzel, Rachel L; Orr, Bradford G; Banaszak Holl, Mark M (2018) Distributions: The Importance of the Chemist's Molecular View for Biological Materials. Biomacromolecules 19:1469-1484
Shakya, Anisha; Dougherty, Casey A; Xue, Yi et al. (2016) Rapid Exchange Between Free and Bound States in RNA-Dendrimer Polyplexes: Implications on the Mechanism of Delivery and Release. Biomacromolecules 17:154-64
Vaidyanathan, Sriram; Chen, Junjie; Orr, Bradford G et al. (2016) Cationic Polymer Intercalation into the Lipid Membrane Enables Intact Polyplex DNA Escape from Endosomes for Gene Delivery. Mol Pharm 13:1967-78
Dougherty, Casey A; Vaidyanathan, Sriram; Orr, Bradford G et al. (2015) Fluorophore:dendrimer ratio impacts cellular uptake and intracellular fluorescence lifetime. Bioconjug Chem 26:304-15
Ma, Qian; Han, Yingchun; Chen, Cong et al. (2015) Oral absorption enhancement of probucol by PEGylated G5 PAMAM dendrimer modified nanoliposomes. Mol Pharm 12:665-74
Manono, Janet; Dougherty, Casey A; Jones, Kirsten et al. (2015) Generation 3 PAMAM dendrimer TAMRA conjugates containing precise dye/dendrimer ratios. Mater Today (Kidlington) 4:86-92
Vaidyanathan, Sriram; Anderson, Kevin B; Merzel, Rachel L et al. (2015) Quantitative Measurement of Cationic Polymer Vector and Polymer-pDNA Polyplex Intercalation into the Cell Plasma Membrane. ACS Nano 9:6097-109
van Dongen, Mallory A; Orr, Bradford G; Banaszak Holl, Mark M (2014) Diffusion NMR study of generation-five PAMAM dendrimer materials. J Phys Chem B 118:7195-202
Rattan, Rahul; Bielinska, Anna U; Banaszak Holl, Mark M (2014) Quantification of cytosolic plasmid DNA degradation using high-throughput sequencing: implications for gene delivery. J Gene Med 16:75-83
Dougherty, Casey A; Furgal, Joseph C; van Dongen, Mallory A et al. (2014) Isolation and characterization of precise dye/dendrimer ratios. Chemistry 20:4638-45

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