Factors That Influence Base-Catalyzed Thiol-Ene Hydrogel Synthesis
Nolan Morrison1, Brandon M Vogel1
1Department of Chemical Engineering, Bucknell University, Lewisburg, PA 17837, USA.
We developed improved ethoxylated trimethylolpropane tri-3-mercaptopropionate (ETTMP) and poly(ethylene glycol) diacrylate (PEGDA) hydrogels for drug delivery. These new hydrogels offer faster gelation and improved storage, enhancing localized drug delivery applications.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Injectable hydrogels for localized drug delivery offer tunable release and non-swelling properties.
- Current ethoxylated trimethylolpropane tri-3-mercaptopropionate (ETTMP) and poly(ethylene glycol) diacrylate (PEGDA) hydrogel synthesis faces challenges including poor solubility, slow gelation, and reproducibility issues.
Purpose of the Study:
- To develop a reliable and reproducible synthesis procedure for ETTMP-PEGDA hydrogels.
- To overcome limitations of existing synthesis methods, including slow gelation and poor ETTMP solubility.
Main Methods:
- Investigated the impact of residual mercaptopropionic acid and alumina purification column height on gelation time.
- Premixed ETTMP and PEGDA to enhance ETTMP solubility in water.
- Conducted a sensitivity analysis of key variables in the synthesis process.
Main Results:
- Achieved hydrogel synthesis with polymer concentrations from 15 to 90 wt%.
- Reduced gelation times to under 2 minutes.
- Obtained tunable hydrogel moduli ranging from 3.5 to 190 kPa.
- Demonstrated ETTMP-PEGDA mixture stability at -20 °C for up to 2 months.
Conclusions:
- The developed synthesis procedure provides a reliable method for producing ETTMP-PEGDA hydrogels.
- These improved hydrogels are suitable for injectable, localized drug delivery with controllable drug release.
- The enhanced storage stability facilitates easier handling, storage, and shipment of the hydrogel precursor mixture.
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