Mechanical Properties of Poly-L-Lysine Hydrogels Across the Helix-Coil Transition
POSTER
Abstract
Poly-L-lysine (PLL) is a biological polyelectrolyte that undergoes structural changes in
response to environmental shifts such as pH. Here, we take advantage of PLL’s structural changes
across the helix-coil transition as a function of pH to develop new functional materials. PLL is
crosslinked with poly (ethylene glycol) diglycidyl ether (EDGE) at crosslink densities, ranging from 3-
6%, and the bulk mechanics of the gel are studied across the coil-helix transition. Dynamic and Dynamic
Small Angle Light Scattering are used to determine the diffusion coefficients of the gel and rheometry is
used to determine shear modulus and strain behavior of the gel as a function of crosslink density, salt,
and pH. Circular Dichroism is used to characterize the helical structure of the PLL in gel. Analyzing the
results of these methods, meshsize is calculated as a function of modulus and volume fraction and
compared to changes in crosslinker % and pH of solution. We find that shear modulus increases as a
function of % crosslinker and mesh size decreases as a function of pH and % crosslinker. By
understanding the hydrogels’ structure and response to environmental changes, we can expand their
potential as functional materials in biomedical applications or soft actuators.
response to environmental shifts such as pH. Here, we take advantage of PLL’s structural changes
across the helix-coil transition as a function of pH to develop new functional materials. PLL is
crosslinked with poly (ethylene glycol) diglycidyl ether (EDGE) at crosslink densities, ranging from 3-
6%, and the bulk mechanics of the gel are studied across the coil-helix transition. Dynamic and Dynamic
Small Angle Light Scattering are used to determine the diffusion coefficients of the gel and rheometry is
used to determine shear modulus and strain behavior of the gel as a function of crosslink density, salt,
and pH. Circular Dichroism is used to characterize the helical structure of the PLL in gel. Analyzing the
results of these methods, meshsize is calculated as a function of modulus and volume fraction and
compared to changes in crosslinker % and pH of solution. We find that shear modulus increases as a
function of % crosslinker and mesh size decreases as a function of pH and % crosslinker. By
understanding the hydrogels’ structure and response to environmental changes, we can expand their
potential as functional materials in biomedical applications or soft actuators.
Presenters
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Alexandra Grinevich
Case Western Reserve University
Authors
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Alexandra Grinevich
Case Western Reserve University