期刊
SPINE
卷 46, 期 4, 页码 E243-E249出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/BRS.0000000000003767
关键词
annulus fibrosus (AF); adhesive biomechanics; cross-linked hydrogel; discectomy; intervertebral disc
资金
- Ministry of Science and Technology, Taiwan [MOST 104-2314-B-016-001, MOST 106-2622-E-002-032-CC2, MOST 107-2221-E-002-068-MY3]
- National Health Research Institute [NHRI-EX109-10924EI]
The study evaluated a newly developed hydrogel for intervertebral disc repair, finding that the hydrogel with 20 mM EDC concentration exhibited good cytocompatibility and degradation rate, making it suitable as a sealant for small AF defects.
Study Design. An in vitro experimental study testing a Gelatin-poly (gamma-glutamic acid) hydrogel for disc repair. Objective. To evaluate the cytocompatibility and degradability of the above mentioned hydrogel for intervertebral disc annular fibrosis (AF) repair. Summary of Background Data. No repair strategies for correcting annular defects in lumbar discectomy have been clinically well recognized. Exogenous supplementation of regenerative materials to fill defects is a minimally invasive way to restore compromised mechanical properties. The injected materials, most commonly gelatin-based materials with cross-linking agents, serve as sealants and as a scaffold for incorporating biomaterials for augmentation. However, cytotoxicity of hydrogel crosslinking agents is of concern in developing viable materials. Methods. This in vitro experimental study evaluated a newly developed gelatin-based hydrogel for intervertebral disc AF repair. Mechanical strength was augmented by gamma-PGA, and 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (EDC) was used for material crosslinking. Isolated bovine tail intervertebral discs (IVDs) were used to test the hydrogel, and hydrogel surface monolayer AF cell culture was used to investigate efficacy in hydrogel constructs of different EDC concentrations. Cell metabolic activity was evaluated with Alamar blue assay, cell viability assay with live/dead stain, and sulfated glycosaminoglycan (GAG) and double strain DNA were quantified to evaluate proliferation of implanted cells and synthesis of extracellular matrix (ECM) proteins. Results. EDC concentrations from 10 to 40 mM resulted in significant decreases in AF cell proliferation without obvious influence on cell viability. Higher EDC concentrations resulted in decreased percentage of Alamar blue reduction and GAG and DNA concentration, but did not affect GAG/DNA and live-dead ratios. Degradation tests revealed that higher EDC concentrations decreased the hydrogel degradation rate. Conclusion. The developed gelatin-poly (gamma-PGA) hydrogel with 20 mM EDC concentration provides an effective gap-filling biomaterial with good cytocompatibility, suggesting substantial promise for use as a sealant for small AF defects.
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