Injectable Hydrogels for Programmable Nanoparticle Release

Injectable hydrogels represent a promising strategy for the extended release of biological molecules, thereby reducing the frequency of injections. This study introduces a novel system based on Michael addition of dextran and polyethylene glycol (PEG) polymers functionalized with oxanorbornadiene (OND) and thiol groups, respectively. Reliable control over gelation speed allows administration by injection using a simple syringe-to-syringe mixing protocol that entrains more than 95% of virus-like particle (VLP) cargo. A combination of retro-Diels-Alder and hydrolytic ester bond cleavage gives rise to programmable release of the VLPs. Different release profiles, including burst, linear, and delayed release over a two-week period, are engineered using different OND linkages, and rheological characterization shows the hydrogels to be well within the desired range of stiffness for subcutaneous use. The modular nature of this system offers a generalizable platform for developing degradable materials aimed at sustained release biomedical applications.

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Publication Details

Journal
Advanced Functional Materials
Published
2024-11-13
DOI
https://doi.org/10.1002/adfm.202409796
Citations
12
Primary Topic
Hydrogels: synthesis, properties, applications
Type
article
Field-Weighted Citation Impact
2.04

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article

Injectable Hydrogels for Programmable Nanoparticle Release

Kasie L. Collins, M. G. Finn, Soumen Das, Dongjing He et al.
12 citations
Advanced Functional Materials
Hydrogels: synthesis, properties, applications
2.04
article

Injectable Hydrogels for Programmable Nanoparticle Release

Kasie L. Collins, M. G. Finn, Soumen Das, Dongjing He, Xi Ying, Wenting Shi, Xuanhao Sheng, Yuhang Hu
article en
12 citations

Abstract

Injectable hydrogels represent a promising strategy for the extended release of biological molecules, thereby reducing the frequency of injections. This study introduces a novel system based on Michael addition of dextran and polyethylene glycol (PEG) polymers functionalized with oxanorbornadiene (OND) and thiol groups, respectively. Reliable control over gelation speed allows administration by injection using a simple syringe-to-syringe mixing protocol that entrains more than 95% of virus-like particle (VLP) cargo. A combination of retro-Diels-Alder and hydrolytic ester bond cleavage gives rise to programmable release of the VLPs. Different release profiles, including burst, linear, and delayed release over a two-week period, are engineered using different OND linkages, and rheological characterization shows the hydrogels to be well within the desired range of stiffness for subcutaneous use. The modular nature of this system offers a generalizable platform for developing degradable materials aimed at sustained release biomedical applications.

Advanced Functional MaterialsVol. 35(1)
Georgia Institute of Technology (US)
Emory University, National Institutes of Health, Wallace H. Coulter Department of Biomedical Engineering, National Cancer Institute, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 12%
Hydrogels: synthesis, properties, applications
2.04
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Injectable Hydrogels for Programmable Nanoparticle Release — Kasie L. Collins, M. G. Finn, et al. · Advanced Functional Materials (2024) | TGRS Research Map | TGRS