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Cellular Encapsulation in 3D Hydrogels for Tissue Engineering
Published on: October 26, 2009
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Comparison of SERS pH probe responses after microencapsulation within hydrogel matrices
Dayle Kotturi1, Sureyya Paterson1, Mike McShane1
1Texas A&M Univ., United States.
Journal of Biomedical Optics
|September 14, 2021
Summary
This study evaluated hydrogels for implanted pH sensors, finding poly(2-hydroxyethyl methacrylate) (pHEMA) to be the most stable over five months for personalized medicine applications.
Area of Science:
- Biomedical Engineering
- Materials Science
- Analytical Chemistry
Background:
- Personalized medicine necessitates continuous monitoring of individual metabolite levels to detect health anomalies and assess medication responses.
- Implanted sensors are crucial for real-time metabolite tracking, requiring accuracy, long-term stability, and biocompatibility.
Purpose of the Study:
- To evaluate four types of hydrogels embedded with pH-sensitive sensors for their suitability in long-term implantation.
- Assessing sensor performance metrics including accuracy, sensitivity, reversibility, longevity, and dynamic response under various conditions.
Main Methods:
- Utilized Raman spectroscopy for calibrating pH-sensitive hydrogel sensors in static and dynamic pH environments.
- Evaluated sensor response times, consistency, and stability after five months of storage.
Main Results:
- All hydrogels enabled surface-enhanced Raman spectroscopy (SERS) sensors to respond to pH without interference, yielding consistent calibration curves.
- Hydrogel probes exhibited slow steady-state response times (several hours), varying among types.
- Poly(2-hydroxyethyl methacrylate) (pHEMA) hydrogels demonstrated the greatest functional stability over five months without significant dynamic range degradation.
Conclusions:
- While all tested hydrogels are potential biocompatible hosts for SERS sensing, pHEMA offers superior long-term functional stability.
- Poly(ethylene glycol) hydrogels show the fastest pH response.
- Both pHEMA and poly(ethylene glycol) hydrogels, being covalently cross-linked and non-degradable, present advantages over sodium alginate for implantable sensor applications.

