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An Injectable AAm-DMAEMA/Alg-Ca2⁺ Gel Designed for Damaged Intervertebral Discs Therapy
Shirong Gu1, Xiaoxia Le2, Mengchao Gu1
1Department of Orthopaedics, The Affiliated Lihuili Hospital of Ningbo University, Ningbo, Zhejiang, 315211, People's Republic of China.
A novel hydrogel, AAm-DMAEMA/Alg-Ca2+, effectively treats intervertebral disc degeneration (IVDD) by promoting cell proliferation and reducing inflammation. This bioactive scaffold shows promise for repairing damaged discs and alleviating low back pain.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Orthopedics
Background:
- Intervertebral disc degeneration (IVDD) is a primary cause of low back pain, significantly impacting individuals and society.
- Bioactive materials offer potential solutions for tissue repair in conditions like IVDD.
Purpose of the Study:
- To design and evaluate a novel calcium alginate-based hydrogel, AAm-DMAEMA/Alg-Ca2+, for its efficacy in treating IVDD.
- To assess the hydrogel's impact on nucleus pulposus (NP) cell behavior and IVDD repair in a rat model.
Main Methods:
- AAm-DMAEMA/Alg-Ca2+ hydrogel morphology was analyzed via SEM.
- IVDD was induced in rats, followed by hydrogel treatment, with assessments including X-ray, MRI, and histological staining.
- In vitro studies used H2O2-induced NP cells to model inflammation, measuring viability, proliferation, and inflammatory markers.
Main Results:
- AAm treatment increased NP cell viability and proliferation by approximately 50%.
- The hydrogel alleviated disc height loss, improved MRI signals, preserved disc structure, and promoted bone formation and chondrogenesis in rats.
- AAm treatment suppressed inflammatory factors (TNF-α, IL-1, IL-6, NLRP3) and reversed H2O2-induced damage to matrix components (Aggrecan, Collagen II) and matrix-degrading enzymes (MMP3/13).
Conclusions:
- AAm-DMAEMA/Alg-Ca2+ hydrogel promotes NP cell proliferation, reduces inflammation, alleviates tissue damage, and enhances bone formation in IVDD.
- This bioactive hydrogel demonstrates significant potential as a therapeutic scaffold for promoting intervertebral disc repair.
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