Single‐component cationic polyethylenimine thermogel for sustained and localized gene delivery to combat multi‐drug resistant cancer

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Single‐component cationic polyethylenimine thermogel for sustained and localized gene delivery to combat multi‐drug resistant cancer
Title:
Single‐component cationic polyethylenimine thermogel for sustained and localized gene delivery to combat multi‐drug resistant cancer
Journal Title:
BMEMat
Publication Date:
24 June 2025
Citation:
Lin, Q., Liu, M., Ke, L., Ong, N. W. X., Wong, J. H. M., Owh, C., Ow, V., Sim, B., Boo, Y. J., Lim, J. Y. C., Wu, Y., & Loh, X. J. (2025). Single‐component cationic polyethylenimine thermogel for sustained and localized gene delivery to combat multi‐drug resistant cancer. BMEMat. Portico. https://doi.org/10.1002/bmm2.70020
Abstract:
Multi‐drug resistant cancer cells with over‐expression of Bcl2 anti‐apoptotic proteins can be effectively killed by transfecting them with Nur77 transcription factor (pNur77). Previous attempts are generally therapeutically unsatisfactory due to low sustained gene expression and are further disadvantaged by their multi‐component designs requiring complicated preparation. Herein, we designed a single cationic amphiphilic copolymer from branched poly(ethylenimine) (PEI‐25k), the gold standard non‐viral vector, that functions simultaneously as the non‐viral vector and hydrogel forming polymeric matrix. Our single‐component hydrogel gene delivery platform is highly facile to prepare as it only requires co‐dissolution of the copolymer with pNur77 to form a homogeneous sol. Due to the high cationic charge density of PEI‐25k, this PEI‐based copolymer effectively complexes a high payload of the plasmid. Subsequently, the copolymer's thermogelling ability enables it to spontaneously self‐assemble into a hydrogel depot by simply being warmed to physiological temperatures upon intra‐tumoral injection. Leveraging upon the high transfection efficiency of PEI‐25k, this PEI‐based thermogel achieved prolonged localized release of pNur77 with high transfection efficiency. This leads to successful tumor size reduction and suppressed tumor reoccurrence in mouse models with low systemic cytotoxicity. We believe this single‐component cationic thermogel non‐viral gene delivery platform is highly attractive for gene therapy.
License type:
Attribution 4.0 International (CC BY 4.0)
Funding Info:
This research / project is supported by the A*STAR - Industry Alignment Fund – Pre-positioning Programme: Ocular Biomaterials for Vitreoretinal Therapeutic Applications
Grant Reference no. : H20c6a0033

This research / project is supported by the National Research Foundation - Thermogels for Therapeutic Applications (THETA)
Grant Reference no. : NRFNRFI07– 2021–0003

This research / project is supported by the Natural Science Foundation of China - NA
Grant Reference no. : 82173750
Description:
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. © 2025 The Author(s). BMEMat published by John Wiley & Sons Australia, Ltd on behalf of Shandong University
ISSN:
2751-7438
2751-7446
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