Literature DB >> 28284104

Development of switchable polymers to address the dilemma of stability and cargo release in polycationic nucleic acid carriers.

Yilong Cheng1, Drew L Sellers1, James-Kevin Y Tan1, David J Peeler1, Philip J Horner2, Suzie H Pun3.   

Abstract

Cationic <n class="Chemical">span class="Chemical">polymern> gene delivery vehicles that effectively resist premature serum degradation often have difficulty releasing their nucleic acid cargoes. In this work, we report a pH-sensitive <spn>an class="Chemical">polymer (SP), poly(oligo(<span class="Chemical">ethylene glycol) monomethyl ether methacrylate)-co-poly(2-(dimethylamino)ethyl methacrylate)-block- poly(propargyl methacrylate-graft-propyl-(4-methoxy-benzylidene)-amine) (p(PMA-PMBA)-b-(p(OEGMA-DMAEMA)), for successful in vitro and in vivo gene transfer. In the physiological condition, the hydrophobization of p(OEGMA-DMAEMA) polycations by p(PMA-PMBA) significantly enhanced the stability of its polyplexes counterpart. In endosomes, the polymer undergoes an acid-triggered hydrophilic transition through the cleavage of benzoic imines, thus allowing the vector to quickly release nucleic acid cargo due to the loss of hydrophobic functionalization. Compared to a pH-insensitive polymer (IP), SP exhibited more significant luciferase plasmid delivery efficiency with HeLa cells in vitro and with in vivo intraventricular brain injections. Therefore, the polymer designed here is a good solution to address the dilemma of stability and cargo release in gene delivery, and may have broad potential applications in therapeutic agent delivery.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Benzoic imine; Gene delivery; Hydrophobization; pH sensitive

Mesh:

Substances:

Year:  2017        PMID: 28284104      PMCID: PMC5382035          DOI: 10.1016/j.biomaterials.2017.02.036

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  31 in total

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