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  4. Decellularized Peripheral Nerve as an Injectable Delivery Vehicle for Neural Applications

Decellularized Peripheral Nerve as an Injectable Delivery Vehicle for Neural Applications

J Biomed Mater Res A, 2022 · DOI: 10.1002/jbm.a.37312 · Published: March 1, 2022

Regenerative MedicineBiomedical

Simple Explanation

Damage to the nervous system can result in loss of sensory and motor function, paralysis, or even death. To facilitate neural regeneration and functional recovery, researchers have employed biomaterials strategies to address both peripheral and central nervous system injuries. Injectable hydrogels that recapitulate native nerve extracellular matrix are especially promising for neural tissue engineering because they offer more flexibility for minimally invasive applications and provide a growth-permissive substrate for neural cell types. Here, we explore the development of injectable hydrogels derived from decellularized rat peripheral nerves (referred to as “injectable peripheral nerve (iPN) hydrogels”), which are processed using a newly developed sodium deoxycholate and DNase (SDD) decellularization method.

Study Duration
Not specified
Participants
Adult male and female Sprague Dawley rats (250-300 g)
Evidence Level
Not specified

Key Findings

  • 1
    The iPN hydrogels thermally gel when exposed to 37°C in under 20 minutes and have mechanical properties similar to neural tissue.
  • 2
    The hydrogels demonstrate in vitro biocompatibility through support of Schwann cell viability and metabolic activity.
  • 3
    Additionally, iPN hydrogels promote greater astrocyte spreading compared to collagen I hydrogels.

Research Summary

In this work, we have optimized the solubilization of decellularized nerve scaffolds, processed using a new sodium deoxycholate and DNase (SDD) decellularization method50, and demonstrated that iPN scaffolds can be successfully generated and have attractive properties for neural repair strategies. The iPN hydrogels form in under 20 minutes and have mechanical properties similar to native neural tissue. Overall, iPN hydrogels generated from SDD method decellularized nerves represent a promising biocompatible platform for development of novel, multi-faceted therapies for neural injury repair.

Practical Implications

Drug Delivery

The iPN hydrogel can be used as a delivery vehicle for drug-loaded microparticles, offering a combinatorial approach to neural injury therapies.

Cell-Based Therapies

The iPN hydrogel can be a potential delivery vehicle for cell-based therapies, given its biocompatibility and support for Schwann cell viability.

Neural Tissue Engineering

The iPN hydrogel represents a promising biocompatible platform for the development of novel therapies for neural injury repair.

Study Limitations

  • 1
    The degradation profile determined in this study was limited, as there were no proteases or cellular influence.
  • 2
    Future studies will focus on encapsulation and release of neurotrophic factors such as BDNF and GDNF, and their physiological effects in vitro and in vivo.
  • 3
    Future experiments will more thoroughly focus on in vitro assessments of nerve regeneration, and eventually in vivo biocompatibility and efficacy.

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