Colloidal Hydrogel with Staged Sequestration and Release of Molecules Undergoing Competitive Binding

Competitive binding of distinct molecules in the hydrogel interior can facilitate dynamic exchange between the hydrogel and the surrounding environment. The ability to control the rates of sequestration and release of these molecules would enhance the hydrogel's functionality and enable targeting of a specific task. Here, we report the design of a colloidal hydrogel with two distinct pore dimensions to achieve staged, diffusion-controlled scavenging and release dynamics of molecules undergoing competitive binding. The staged scavenging and release strategy was shown for CpG oligodeoxynucleotide (ODN) and human epidermal growth factor (hEGF), two molecules exhibiting different affinities to the quaternary ammonium groups of the hydrogel. Fast ODN scavenging from the ambient environment occurred via diffusion through submicrometer-size hydrogel pores, while delayed hEGF release from the hydrogel was governed by its diffusion through nanometer-size pores. The results of the experiments were in agreement with simulation results. The significance of staged ODN-hEGF exchange was highlighted by the dual anti-inflammation and tissue proliferation hydrogel performance.

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Publication Details

Journal
ACS Nano
Published
2024-09-06
DOI
https://doi.org/10.1021/acsnano.4c09342
Citations
12
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
2.21

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article

Colloidal Hydrogel with Staged Sequestration and Release of Molecules Undergoing Competitive Binding

Hani E. Naguib, Gilbert C. Walker, Yingshan Ma, Eugenia Kumacheva et al.
12 citations
ACS Nano
3D Printing in Biomedical Research
2.21
article

Colloidal Hydrogel with Staged Sequestration and Release of Molecules Undergoing Competitive Binding

Hani E. Naguib, Gilbert C. Walker, Yingshan Ma, Eugenia Kumacheva, Terek Li, Nashmia Zia, Yuhang Huang
article en
12 citations

Abstract

Competitive binding of distinct molecules in the hydrogel interior can facilitate dynamic exchange between the hydrogel and the surrounding environment. The ability to control the rates of sequestration and release of these molecules would enhance the hydrogel's functionality and enable targeting of a specific task. Here, we report the design of a colloidal hydrogel with two distinct pore dimensions to achieve staged, diffusion-controlled scavenging and release dynamics of molecules undergoing competitive binding. The staged scavenging and release strategy was shown for CpG oligodeoxynucleotide (ODN) and human epidermal growth factor (hEGF), two molecules exhibiting different affinities to the quaternary ammonium groups of the hydrogel. Fast ODN scavenging from the ambient environment occurred via diffusion through submicrometer-size hydrogel pores, while delayed hEGF release from the hydrogel was governed by its diffusion through nanometer-size pores. The results of the experiments were in agreement with simulation results. The significance of staged ODN-hEGF exchange was highlighted by the dual anti-inflammation and tissue proliferation hydrogel performance.

ACS NanoVol. 18(37)
University of Toronto (CA)
Natural Sciences and Engineering Research Council of Canada
Clean water and sanitation
Openalex Percentile: Top 12%
3D Printing in Biomedical Research
2.21
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