skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Macromolecular Solute Transport in Supramolecular Hydrogels Spanning Dynamic to Quasi-Static States
Hydrogels prepared from supramolecular cross-linking motifs are appealing for use as biomaterials and drug delivery technologies. The inclusion of macromolecules (e.g., protein therapeutics) in these materials is relevant to many of their intended uses. However, the impact of dynamic network cross-linking on macromolecule diffusion must be better understood. Here, hydrogel networks with identical topology but disparate cross-link dynamics are explored. These materials are prepared from cross-linking with host–guest complexes of the cucurbit[7]uril (CB[7]) macrocycle and two guests of different affinity. Rheology confirms differences in bulk material dynamics arising from differences in cross-link thermodynamics. Fluorescence recovery after photobleaching (FRAP) provides insight into macromolecule diffusion as a function of probe molecular weight and hydrogel network dynamics. Together, both rheology and FRAP enable the estimation of the mean network mesh size, which is then related to the solute hydrodynamic diameters to further understand macromolecule diffusion. Interestingly, the thermodynamics of host–guest cross-linking are correlated with a marked deviation from classical diffusion behavior for higher molecular weight probes, yielding solute aggregation in high-affinity networks. These studies offer insights into fundamental macromolecular transport phenomena as they relate to the association dynamics of supramolecular networks. Translation of these materials from in vitro to in vivo is also assessed by bulk release of an encapsulated macromolecule. Contradictory in vitro to in vivo results with inverse relationships in release between the two hydrogels underscores the caution demanded when translating supramolecular biomaterials into application.  more » « less
Award ID(s):
1944875
PAR ID:
10398890
Author(s) / Creator(s):
; ; ; ; ; ;
Publisher / Repository:
American Chemical Society
Date Published:
Journal Name:
ACS Applied Bio Materials
ISSN:
2576-6422
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Host–guest interactions have been increasingly explored for use in the dynamic physical crosslinking of polymeric precursors to form hydrogel networks. However, the orientation of guest motifs is restricted upon macromolecule conjugation. The implications of such restriction on both the kinetics and thermodynamics of the resulting host–guest supramolecular crosslinks are poorly understood. Herein, guest crosslinking motifs from controlled regioisomers are demonstrated to yield distinct material properties. Moreover, the underlying phenomena point to further unexpected impact of modular guest topology manifest on the molecular scale in both the affinity and dynamics of supramolecular complex formation. 
    more » « less
  2. Abstract Dynamic hydrogel crosslinking captures network reorganization and self‐healing of natural materials, yet is often accompanied by reduced mechanical properties compared to covalent analogs. Toughening is possible in certain materials with processing by directional freeze‐casting and salting‐out, producing hierarchically organized networks with directionally enhanced mechanical properties. The implications of including dynamic supramolecular crosslinking alongside such processes are unclear. Here, a supramolecular hydrogel prepared from homoternary crosslinking by pendant guests with a free macrocycle is subsequently processed by directional freeze‐casting and salting‐out. The resulting hydrogels tolerate multiple cycles of compression. Excitingly, supramolecular affinity dictates the mechanical properties of the bulk hydrogels, with higher affinity interactions producing materials with higher Young's modulus and enhanced toughness under compression. The importance of supramolecular crosslinking is emphasized with a supramolecular complex that is converted in situ into a covalent crosslink. While supramolecular hydrogels do not fracture and spontaneously self‐heal when cut, their covalent analogs fracture under moderate strain and do not self‐heal. This work shows a molecular‐scale origin of bulk hydrogel toughening attributed to affinity and dynamics of supramolecular crosslinking, offering synergy in combination with bulk post‐processing techniques to yield materials with enhanced mechanical properties tunable at the molecular scale for the needs of specific applications. 
    more » « less
  3. Controlled-release materials are desirable for many delivery applications and have been used to improve the efficiency of fertilizers and pesticides in crop management. Due to their potential to reduce application of toxic chemicals while prolonging exposure to active agents, controlled-release nanomaterials are currently being investigated for increasing agricultural production and preventing overfertilization. Hydrogels are underexplored as controlled-release nanomaterials and can deliver many types of cargo, from metal ions to small molecules. Alginate-based hydrogels are biocompatible and their internal carboxylic acids coordinate agriculturally valuable micronutrients like Cu2+, Zn2+, and Ca2+. Hydrogels comprising ionic and nonionic polymers can coordinate agriculturally valuable micronutrients, and the combination of ionic and nonionic polymers results in hydrogels with tunable release profiles. Alginate, for example, contains carboxylates that ionically cross-link with divalent cations like Cu2+, Zn2+, and Ca2+, while polar moieties on chitin enable nonionic coordination. To our knowledge, soft-material copper-loaded nanoparticles have not yet been applied as controlled-release materials for foliar delivery. In this work, we present the synthesis and micronutrient release characteristics of hydrogel nanoparticles containing Cu2+, which is coordinated by ionic and nonionic polymers. Hydrogel nanoparticles (HNPs) were prepared by liquid–liquid emulsion techniques and cross-linked with Cu2+ to form double-network hydrogels made from alginate and non-cross-linking chitin. Nanoparticles (100–300 nm in diameter) were characterized by cryogenic electron microscopy, nanoparticle tracking analysis, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The copper release profiles of HNPs with different polymer compositions were compared. HNPs containing both chitin and alginate released 8–20 times more copper than HNPs with alginate alone, suggesting that the presence of non-cross-linking polymers improves copper release. Thus, HNP delivery characteristics can be tuned by manipulating intraparticle bond dynamics in the hydrogel polymer matrix. 
    more » « less
  4. Abstract The transient self‐assembly of molecules under the direction of a consumable fuel source is fundamental to biological processes such as cellular organization and motility. Such biomolecular assemblies exist in an out‐of‐equilibrium state, requiring continuous consumption of high energy molecules. At the same time, the creation of bioinspired supramolecular hydrogels has traditionally focused on associations occurring at the thermodynamic equilibrium state. Here, hydrogels are prepared from cucurbit[7]uril host–guest supramolecular interactions through transient physical crosslinking driven by the consumption of a reactive chemical fuel. Upon action from this fuel, the affinity and dynamics of CB[7]–guest recognition are altered. In this way, the lifetime of transient hydrogel formation and the dynamic modulus obtained are governed by fuel consumption, rather than being directed by equilibrium complex formation. 
    more » « less
  5. Abstract Controlled degradation of hydrogels enables several applications of these materials, including controlled drug and cell release applications and directed growth of neural networks. These applications motivate the need of a simulation framework for modeling controlled degradation in hydrogels. We develop a Dissipative Particle Dynamics (DPD) framework for hydrogel degradation. As a model hydrogel, we prepare a network formed by end-linking tetra-arm polyethylene glycol precursors. We model bond breaking during degradation of this hydrogel as a stochastic process. The fraction of degradable bonds follows first order degradation kinetics. We characterize the rate of mass loss during degradation process. 
    more » « less