Literature DB >> 25862514

Multifunctional poly(methacrylate) polyplex libraries: A platform for gene delivery inspired by nature.

M E Favretto1, A Krieg2, S Schubert3, U S Schubert2, R Brock4.   

Abstract

Polymer-based gene delivery systems have enormous potential in biomedicine, but their efficiency is often limited by poor biocompatibility. Poly(methacrylate)s (PMAs) are an interesting class of polymers which allow to explore structure-activity relationships of polymer functionalities for polyplex formation in oligonucleotide delivery. Here, we synthesized and tested a library of PMA polymers, containing functional groups contributing to the different steps of gene delivery, from oligonucleotide complexation to cellular internalization and endosomal escape. By variation of the molar ratios of the individual building blocks, the physicochemical properties of the polymers and polyplexes were fine-tuned to reduce toxicity as well as to increase activity of the polyplexes. To further enhance transfection efficiency, a cell-penetrating peptide (CPP)-like functionality was introduced on the polymeric backbone. With the ability to synthesize large libraries of polymers in parallel we also developed a workflow for a mid-to-high throughput screening, focusing first on safety parameters that are accessible by high-throughput approaches such as blood compatibility and toxicity towards host cells and only at a later stage on more laborious tests for the ability to deliver oligonucleotides. To arrive at a better understanding of the molecular basis of activity, furthermore, the effect of the presence of heparan sulfates on the surface of host cells was assessed and the mechanism of cell entry and intracellular trafficking investigated for those polymers that showed a suitable pharmacological profile. Following endocytic uptake, rapid endosomal release occurred. Interestingly, the presence of heparan sulfates on the cell surface had a negative impact on the activity of those polyplexes that were sensitive to decomplexation by heparin in solution. In summary, the screening approach identified two polymers, which form polyplexes with high stability and transfection capacity exceeding the one of poly(ethylene imine) also in the presence of serum.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Blood compatibility; Gene delivery; Oligonucleotides; Poly(methacrylate)s; Polyplex; Screening strategies

Mesh:

Substances:

Year:  2015        PMID: 25862514     DOI: 10.1016/j.jconrel.2015.04.005

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  3 in total

Review 1.  Exploring the role of polymer structure on intracellular nucleic acid delivery via polymeric nanoparticles.

Authors:  Corey J Bishop; Kristen L Kozielski; Jordan J Green
Journal:  J Control Release       Date:  2015-10-01       Impact factor: 9.776

2.  Cationic β-Cyclodextrin-Chitosan Conjugates as Potential Carrier for pmCherry-C1 Gene Delivery.

Authors:  Touba Eslaminejad; Seyed Noureddin Nematollahi-Mahani; Mehdi Ansari
Journal:  Mol Biotechnol       Date:  2016-04       Impact factor: 2.695

3.  Multivalent cationic pseudopeptide polyplexes as a tool for cancer therapy.

Authors:  Zoi Diamantopoulou; Maud-Emmanuelle Gilles; Maha Sader; Mélissande Cossutta; Benoit Vallée; Claire Houppe; Damien Habert; Blandine Brissault; Eric Leroy; Federica Maione; Enrico Giraudo; Damien Destouches; Jacques Penelle; José Courty; Ilaria Cascone
Journal:  Oncotarget       Date:  2017-09-30
  3 in total

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