Literature DB >> 15614818

Structure/function relationships of polyamidoamine/DNA dendrimers as gene delivery vehicles.

Chad S Braun1, Joseph A Vetro, Donald A Tomalia, Gary S Koe, Janet G Koe, C Russell Middaugh.   

Abstract

PAMAM dendrimers are members of a class of polyamine polymers that demonstrate significant gene delivery ability. In this study, a selection of PAMAM dendrimers, spanning a range of sizes (generations 2, 4, 7, and 9) and transfection efficiencies, are characterized by various biophysical methods to search for structural properties that correlate with transfection. Measurements of colloidal properties (size and zeta potential) as a function of charge ratio reveal that highly transfecting dendrimer/DNA complexes have size/zeta potential values between 4 and 8. Circular dichroism (CD) and FTIR spectroscopy of complexes confirm the DNA component remains in B form when associated with all dendrimer generations up to a 5:1 charge ratio (+/-). Isothermal titration calorimetry and differential scanning calorimetry detect changes that are related to polymer structure and charge ratio but do not directly correlate with transfection efficiency. Despite DNA structural and stability changes detected by CD, FTIR, DSC, and ITC that are similar to those seen with other cationic delivery vehicles [e.g., cationic lipids, peptoids/lipitoids, peptides, polyethyleneimines (PEIs), etc.], clear correlations with transfection activity are not readily apparent. This may be due, at least in part, to the heterogeneity of the complexes. Copyright 2004 Wiley-Liss, Inc.

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Year:  2005        PMID: 15614818     DOI: 10.1002/jps.20251

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  45 in total

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7.  PEGylated polyamidoamine dendrimers with bis-aryl hydrazone linkages for enhanced gene delivery.

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Review 8.  Nanoparticle-mediated brain-specific drug delivery, imaging, and diagnosis.

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9.  Labile catalytic packaging of DNA/siRNA: control of gold nanoparticles "out" of DNA/siRNA complexes.

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10.  An efficient, non-viral dendritic vector for gene delivery in tissue engineering.

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Journal:  Gene Ther       Date:  2017-09-14       Impact factor: 5.250

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