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      Influence of Oligospermines Architecture on Their Suitability for siRNA Delivery

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          Abstract

          Spermines are naturally abundant polyamines that partially condense nucleic acids and exhibit the proton-sponge effect in an acidic environment. However, spermines show a limited efficiency for transfecting nucleic acids because of their low molecular weight. Therefore, spermines need to be modified to be used as nonviral vectors for nucleic acids. Here, we synthesized linear bisspermine as well as a linear and dendritic tetraspermine with different molecular architectures. These oligospermines were self-assembled into polyplexes with siRNA. The structure–activity relationship of the oligospermines was evaluated in terms of their efficiency for delivering siRNA into a nonsmall cell lung carcinoma cell line. Oligospermines displayed minimal cytotoxicity but efficient siRNA condensation and showed better stability against polyanions than polyethylenimine. The morphology of the polyplexes was strongly affected by the oligospermine architecture. Linear tetraspermine/siRNA polyplexes showed the best gene-silencing efficiency among the oligospermines tested at both the mRNA and protein expression levels, indicating the most favorable structure for siRNA delivery.

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          Nonviral vectors for gene delivery.

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            Polyamines.

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              Gene silencing in mammals by small interfering RNAs.

              Among the 3 billion base pairs of the human genome, there are approximately 30,000-40,000 protein-coding genes, but the function of at least half of them remains unknown. A new tool - short interfering RNAs (siRNAs) - has now been developed for systematically deciphering the functions and interactions of these thousands of genes. siRNAs are an intermediate of RNA interference, the process by which double-stranded RNA silences homologous genes. Although the use of siRNAs to silence genes in vertebrate cells was only reported a year ago, the emerging literature indicates that most vertebrate genes can be studied with this technology.
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                Author and article information

                Journal
                Biomacromolecules
                Biomacromolecules
                bm
                bomaf6
                Biomacromolecules
                American Chemical Society
                1525-7797
                1526-4602
                19 February 2015
                19 February 2014
                14 April 2014
                : 15
                : 4
                : 1299-1310
                Affiliations
                []Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University , 259 Mack Avenue, Detroit, Michigan 48201, United States
                []Department of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois , 1601 Parkview Avenue, Rockford, Illinois 61107, United States
                [§ ]Molecular Therapeutics Program, Barbara Ann Karmanos Cancer Institute , Detroit, Michigan 48201, United States
                Author notes
                [* ]Phone: 313-577-1523; Fax: 313-577-2033; E-mail: olivia.merkel@ 123456wayne.edu .
                Article
                10.1021/bm401849d
                3993926
                24552396
                11dd05b8-23eb-4b2a-8fc9-1bf7895fbc1b
                Copyright © 2014 American Chemical Society
                History
                : 17 December 2013
                : 12 February 2014
                Funding
                National Institutes of Health, United States
                Categories
                Article
                Custom metadata
                bm401849d
                bm-2013-01849d

                Biochemistry
                Biochemistry

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