Dendrimers are an understudied class of nanometer-scale, globular polymers that offer candidates for the next-generation of polymer therapeutics. Size, shape, and composition impact all aspects of these vehicles including overall efficacy, bioavailability, toxicity, metabolism, absorption and excretion. Optimization of these parameters for drug delivery using dendrimers requires (1) exquisite control over the synthesis of dendrimer candidates; (2) an understanding of the physical organic chemistry of these macromolecules and macromolecule-drug complexes; and finally, (3) assessment of therapeutic efficacy. To date, owing to synthetic routes that lack an approach for systematic variation of size, shape, and composition as well as number of architectures for structure-property relationships (the hallmark of physical organic chemistry), there is little fundamental understanding of the design criteria for the use of dendrimers in drug delivery. There are three overall aims of proposed research which focuses on breast and prostate tumors: ? ? Specific Aim #1: Examine the fundamental physical organic chemistry of these macromolecules as it pertains to: 1 A) The number of """"""""phases"""""""" a biocompatible PEGylated dendrimer comprises in water and the impact that this has on the sequestration of drugs: In monophasic dendrimers, sequestration is proportional to MW. 1B) The ability to tailor release rates of drugs through systematic cleavage of bioloabile linkers in architectures showing a gradient of tethers and steric crowding. 1C) The global conformation of these macromolecules and the guests associated with them. ? ? Specific Aim #2: Identify the molecular determinants for biodistribution and tumor targeting using multifuctional dendrimers. ? ? Specific Aim #3: Explore macromolecular recognition to determine the molecular parameters that allow these dendrimers to serve as synthetic vaccines and as multi-functional adaptor units on antibodies. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM064560-05
Application #
7146967
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Fabian, Miles
Project Start
2001-12-01
Project End
2010-07-31
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
5
Fiscal Year
2006
Total Cost
$260,343
Indirect Cost
Name
Texas A&M University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
078592789
City
College Station
State
TX
Country
United States
Zip Code
77845
Lim, Jongdoo; Kostiainen, Mauri; Maly, Jan et al. (2013) Synthesis of large dendrimers with the dimensions of small viruses. J Am Chem Soc 135:4660-3
Lim, Jongdoo; Pavan, Giovanni M; Annunziata, Onofrio et al. (2012) Experimental and computational evidence for an inversion in guest capacity in high-generation triazine dendrimer hosts. J Am Chem Soc 134:1942-5
Barata, Teresa; Teo, Ian; Lalwani, Sanjiv et al. (2011) Computational design principles for bioactive dendrimer based constructs as antagonists of the TLR4-MD-2-LPS complex. Biomaterials 32:8702-11
Merkel, Olivia M; Zheng, Mengyao; Mintzer, Meredith A et al. (2011) Molecular modeling and in vivo imaging can identify successful flexible triazine dendrimer-based siRNA delivery systems. J Control Release 153:23-33
Pavan, Giovanni M; Mintzer, Meredith A; Simanek, Eric E et al. (2010) Computational insights into the interactions between DNA and siRNA with ""rigid"" and ""flexible"" triazine dendrimers. Biomacromolecules 11:721-30
Lo, Su-Tang; Stern, Stephan; Clogston, Jeffrey D et al. (2010) Biological assessment of triazine dendrimer: toxicological profiles, solution behavior, biodistribution, drug release and efficacy in a PEGylated, paclitaxel construct. Mol Pharm 7:993-1006
Lim, Jongdoo; Venditto, Vincent J; Simanek, Eric E (2010) Synthesis and characterization of a triazine dendrimer that sequesters iron(III) using 12 desferrioxamine B groups. Bioorg Med Chem 18:5749-53
Lim, Jongdoo; Mintzer, Meredith A; Perez, Lisa M et al. (2010) Synthesis of odd generation triazine dendrimers using a divergent, macromonomer approach. Org Lett 12:1148-51
Merkel, Olivia M; Mintzer, Meredith A; Simanek, Eric E et al. (2010) Perfectly shaped siRNA delivery. Ther Deliv 1:737-42
Lim, Jongdoo; Pellois, Jean-Philippe; Simanek, Eric E (2010) A retro-inverso TAT-like peptide designed to deliver cysteamine to cells. Bioorg Med Chem Lett 20:6321-3

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