Hybrid Poly(β‐amino ester) Triblock Copolymers Utilizing a RAFT Polymerization Grafting‐From Methodology

Author:

Kasza Karolina12ORCID,Elsherbeny Amr134ORCID,Moloney Cara4ORCID,Hardie Kim R.2ORCID,Cámara Miguel2ORCID,Alexander Cameron1ORCID,Gurnani Pratik5ORCID

Affiliation:

1. Division of Molecular Therapeutics and Formulation School of Pharmacy University of Nottingham Nottingham NG7 2RD UK

2. National Biofilms Innovation Centre School of Life Sciences, Biodiscovery Institute University Park, University of Nottingham Nottingham NG7 2RD UK

3. Ex Vivo Cancer Pharmacology Centre of Excellence School of Medicine University of Nottingham Nottingham NG7 2RD UK

4. School of Medicine Biodiscovery Institute University Park, University of Nottingham Nottingham NG7 2RD UK

5. UCL School of Pharmacy University College London 29–39 Brunswick Square London WC1N 1AX UK

Abstract

AbstractThe biocompatibility, biodegradability, and responsiveness of poly(β‐amino esters) (PBAEs) has led to their widespread use as biomaterials for drug and gene delivery. Nonetheless, the step‐growth polymerization mechanism that yields PBAEs limits the scope for their structural optimization toward specific applications because of limited monomer choice and end‐group modifications. Moreover, to date the post‐synthetic functionalization of PBAEs has relied on grafting‐to approaches, challenged by the need for efficient polymer–polymer coupling and potentially difficult post‐conjugation purification. Here a novel grafting‐from approach to grow reversible addition–fragmentation chain transfer (RAFT) polymers from a PBAE scaffold is described. This is achieved through PBAE conversion into a macromolecular chain transfer agent through a multistep capping procedure, followed by RAFT polymerization with a range of monomers to produce PBAE–RAFT hybrid triblock copolymers. Following successful synthesis, the potential biological applications of these ABA triblock copolymers are illustrated through assembly into polymeric micelles and encapsulation of a model hydrophobic drug, followed by successful nanoparticle (NP) uptake in breast cancer cells. The findings demonstrate this novel synthetic methodology can expand the scope of PBAEs as biomaterials.

Funder

Biotechnology and Biological Sciences Research Council

Wellcome Trust

Publisher

Wiley

Subject

Materials Chemistry,Organic Chemistry,Polymers and Plastics,Physical and Theoretical Chemistry,Condensed Matter Physics

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