TY - JOUR
T1 - Probing the microenvironment of polyacrylamide hydrogel matrix using turbidity and fluorescence recovery after photobleaching
T2 - One versus Two phases
AU - Khandai, Santripti
AU - Siegel, Ronald A.
AU - Jena, Sidhartha S.
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/5/20
Y1 - 2020/5/20
N2 - The microstructure of polyacrylamide hydrogel matrices was probed by turbidity measurements, and by fluorescence recovery after photobleaching (FRAP) of fluorescently labeled bovine serum albumin (fBSA), as a function of polymer concentration and crosslink density. Turbidity increased with increasing polymer and/or crosslinker concentration. At low polymer and crosslinker concentrations, FRAP dynamics were well described by diffusion through a single polymer phase. However for higher concentrations of polymer and crosslinker, the diffusion model was inadequate, and a second mode, likely corresponding to release of fBSA from regions of relatively dense polymer, was observed. At low network concentrations, probe diffusivity (inversely related to FRAP relaxation time) decreased with increasing polymer and crosslinker concentrations. Following onset of the second mode, however, diffusivity increased with increasing monomer concentration, suggesting that the network through which fBSA diffused became looser. The optical and FRAP measurements, while showing qualitatively similar trends, were not directly correlated, and they likely reflected different modes of network phase separation.
AB - The microstructure of polyacrylamide hydrogel matrices was probed by turbidity measurements, and by fluorescence recovery after photobleaching (FRAP) of fluorescently labeled bovine serum albumin (fBSA), as a function of polymer concentration and crosslink density. Turbidity increased with increasing polymer and/or crosslinker concentration. At low polymer and crosslinker concentrations, FRAP dynamics were well described by diffusion through a single polymer phase. However for higher concentrations of polymer and crosslinker, the diffusion model was inadequate, and a second mode, likely corresponding to release of fBSA from regions of relatively dense polymer, was observed. At low network concentrations, probe diffusivity (inversely related to FRAP relaxation time) decreased with increasing polymer and crosslinker concentrations. Following onset of the second mode, however, diffusivity increased with increasing monomer concentration, suggesting that the network through which fBSA diffused became looser. The optical and FRAP measurements, while showing qualitatively similar trends, were not directly correlated, and they likely reflected different modes of network phase separation.
KW - Diffusion
KW - FRAP
KW - Gels
KW - Phase separation
KW - Turbidity
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U2 - 10.1016/j.colsurfa.2020.124618
DO - 10.1016/j.colsurfa.2020.124618
M3 - Article
AN - SCOPUS:85080083854
SN - 0927-7757
VL - 593
JO - Colloids and Surfaces A: Physicochemical and Engineering Aspects
JF - Colloids and Surfaces A: Physicochemical and Engineering Aspects
M1 - 124618
ER -