3.8 Article

Guest-Host Supramolecular Assembly of Injectable Hydrogel Nanofibers for Cell Encapsulation

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 7, 期 9, 页码 4164-4174

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.1c00275

关键词

hydrogel; nanofibers; injectable; supramolecular

资金

  1. University of Virginia
  2. DoD [W81XWH-19-1-0157]
  3. NIH [R21AR075181]

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This study developed a mechanically robust fibrous hydrogel with shear-thinning behavior, rapid self-healing, and cytocompatibility, suitable for minimally invasive delivery. Human mesenchymal stromal cells encapsulated in this fibrous hydrogel showed high viability and enhanced cell spreading and alignment, demonstrating its potential for cell and tissue engineering applications.
The fibrous architecture of the extracellular matrix (ECM) is recognized as an integral regulator of cell function. However, there is an unmet need to develop mechanically robust biomaterials mimicking nanofibrous tissue topography that are also injectable to enable minimally invasive delivery. In this study, we have developed a fibrous hydrogel composed of supramolecularly assembled hyaluronic acid (HA) nanofibers that exhibits mechanical integrity, shear-thinning behavior, rapid self-healing, and cytocompatibility. HA was modified with methacrylates to permit fiber photo-cross-linking following electrospinning and either guest adamantane or host beta-cyclodextrin groups to guide supramolecular fibrous hydrogel assembly. Analysis of fibrous hydrogel rheological properties showed that the mixed guest-host fibrous hydrogel was more mechanically robust (6.6 +/- 2.0 kPa, storage modulus (G')) than unmixed guest hydrogel fibers (1.0 +/- 0.1 kPa) or host hydrogel fibers (1.1 +/- 0.1 kPa) separately. The reversible nature of the guest-host supramolecular interactions also allowed for shear-thinning and self-healing behavior as demonstrated by cyclic deformation testing. Human mesenchymal stromal cells (hMSCs) encapsulated in fibrous hydrogels demonstrated satisfactory viability following injection and after 7 days of culture (>85%). Encapsulated hMSCs were more spread and elongated when cultured in viscoelastic guest-host hydrogels compared to nonfibrous elastic controls, with hMSCs also showing significantly decreased circularity in fibrous guest-host hydrogels compared to nonfibrous guest-host hydrogels. Together, these data highlight the potential of this injectable fibrous hydrogel platform for cell and tissue engineering applications requiring minimally invasive delivery.

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