Neutral Block Copolymer Assisted Gene Delivery using Hydrodynamic Limb Vein Injection

Author:

Guen Yann Le12,Delecourt Gwendoline3,Gall Tony Le1,Du Haiqin3,Illy Nicolas3,Huin Cécile34,Bennevault Véronique34,Midoux Patrick5,Montier Tristan12,Guégan Philippe3ORCID

Affiliation:

1. Univ Brest INSERM EFS UMR 1078 GGB‐GTCA Team Brest F‐29200 France

2. CHU de Brest Service de Génétique Médicale et de Biologie de la Reproduction Centre de Référence des Maladies Rares Maladies Neuromusculaires Brest 29200 France

3. Institut Parisien de Chimie Moléculaire Equipe Chimie des Polymères Sorbonne University UMR 8232 CNRS Paris 75005 France

4. University of Evry Essonne Evry 91000 France

5. Centre de Biophysique Moléculaire CNRS UPR4301 Orléans 45100 France

Abstract

AbstractThree different amphiphilic block copolymer families are synthesized to investigate new opportunities to enhance gene delivery via Hydrodynamic Limb Vein (HLV) injections. First a polyoxazoline‐based family containing mostly one poly(2‐methyl‐2‐oxazoline) (PMeOx) block and a second block POx with an ethyl (EtOx), isopropyl (iPrOx) or phenyl substituent (PhOx) is synthesized. Then an ABC poly(2‐ethyl‐2‐oxazoline)‐b‐poly(2‐n‐propyl‐2‐oxazoline)‐b‐poly(2‐methyl‐2‐oxazoline) triblock copolymer is synthesized, with a thermosensitive middle block. Finally, polyglycidol‐b‐polybutylenoxide‐b‐polyglycidol copolymers with various molar masses and amphiphilic balance are produced. The simple architecture of neutral amphiphilic triblock copolymer is not sufficient to obtain enhanced in vivo gene transfection. Double or triple amphiphilic neutral block copolymers are improving the in vivo transfection performances through HLV administration as far as a block having an lower critical solution temperature is incorporated in the vector. The molar mass of the copolymer does not seem to affect the vector performances in a significant manner.

Funder

French Muscular Dystrophy Association

Agence Nationale de la Recherche

Publisher

Wiley

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