In Situ Measurement of Thermodynamic Partitioning in Open Hydrogels.
Alison SuBenjamin E SmithAmy E HerrPublished in: Analytical chemistry (2019)
Thermodynamic partitioning dictates solute loading and release from a hydrogel. Design of drug delivery vehicles, cell and tissue matrices, and immunoassay scaffolds that utilize hydrogel materials is informed by an understanding of the thermodynamic partitioning properties of those hydrogels. We develop aberration-compensated laser scanning confocal microscopy (AC-LSCM), a technique that can be applied to all fluorescence microscopy-based equilibrium partition coefficient measurements where the fluorescence is uniformly distributed in the reference material (e.g., many solutes in thermodynamic equilibrium). In this paper, we use AC-LSCM to measure spatially resolved in situ equilibrium partition coefficients of various fluorescently labeled solutes in single-layer and multilayer open hydrogels. In considering a dynamic material, we scrutinize solute interactions with a UV photoactive polyacrylamide gel that incorporates a benzophenone methacrylamide backbone. We observed strong agreement with an adjusted version of Ogston's ideal size-exclusion model for spatially resolved in situ equilibrium partition coefficients across a wide range of polyacrylamide hydrogel densities (R2 = 0.98). Partition coefficients of solutes differing in hydrodynamic radius were consistent with size-based theory in the photoactive hydrogels, but exceed those in unmodified polyacrylamide gels. This observation suggests a deviation from the size-exclusion model and a shift in the thermodynamic equilibrium state of the solutes toward the gel phase. AC-LSCM also resolves differential partitioning behavior of the model solute in two-layer gels, providing insight into the transport phenomena governing the partitioning in multilaminate gel structures. Furthermore, AC-LSCM identifies and quantifies depth-dependent axial aberrations that could confound quantitation, highlighting the need for the "aberration compensated" aspect of AC-LSCM.
Keyphrases
- drug delivery
- aqueous solution
- hyaluronic acid
- wound healing
- tissue engineering
- molecular dynamics
- molecular dynamics simulations
- drug release
- cancer therapy
- high resolution
- single molecule
- minimally invasive
- optical coherence tomography
- genome wide
- ms ms
- mass spectrometry
- extracellular matrix
- magnetic resonance imaging
- single cell
- dna methylation
- energy transfer
- cell therapy
- magnetic resonance
- positron emission tomography
- pet imaging
- quantum dots
- diffusion weighted imaging