Evidence map›Paper›PMID 41904497›Full record

ArticleJournal of orthopaedic surgery and research2026

Supercritical carbon dioxide decellularization of porcine annulus fibrosus for regenerative medicine.

Lien-Chen Wu, Yueh-Ying Hsieh, Chia-Hsien Chen, Ting-Shuo Hsu, Chang-Jung Chiang

Abstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lien-Chen WuDepartment of Orthopedics, Wan Fang Hospital, Taipei Medical University, Taipei City, 116079, Taiwan.
Yueh-Ying HsiehDepartment of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei City, 110301, Taiwan.
Chia-Hsien ChenDepartment of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei City, 110301, Taiwan.
Ting-Shuo HsuDepartment of Orthopedics, Shuang Ho Hospital, Taipei Medical University, New Taipei City, 235041, Taiwan.
Chang-Jung ChiangDepartment of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei City, 110301, Taiwan. cjchiang@s.tmu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundScaffold implantation has emerged as a promising therapeutic strategy for the repair of intervertebral disc (IVD) herniation and degeneration. Decellularized scaffolds enhance the biocompatibility and feasibility of xenogeneic transplantation; however, conventional decellularization methods may introduce cytotoxic residues that impair IVD regeneration. In this study, we utilized supercritical CO

methodsBy combining freeze-thaw cycles with scCO

resultsOur findings indicate that this method effectively disrupts cellular components while significantly reducing residual nucleic acids and α-Gal xenogeneic antigens, thereby lowering immunogenicity. Importantly, the decellularization process preserved collagen content without causing denaturation or degradation. Although glycosaminoglycan (GAG) content was reduced, the porous structure of the scaffolds remained intact, which is critical for nutrient diffusion and potential cell infiltration following implantation. Furthermore, the decellularized scaffolds were processed under conditions expected to minimize biological contamination, suggesting their potential suitability for subsequent biomedical applications.

conclusionsThese results demonstrate that the optimized decellularization method can generate structurally preserved annulus fibrosus scaffolds with reduced immunogenic components, supporting their potential application in spinal tissue engineering.

trial registrationNot applicable.

Indexed as

Annulus FibrosusCarbon DioxideDecellularized Extracellular MatrixRegenerative MedicineTissue EngineeringTissue ScaffoldsAnimalsCollagenGlycosaminoglycansSwineCarbon DioxideCollagenDecellularized Extracellular MatrixGlycosaminoglycansAnnulus fibrosus (AF)DecellularizationIntervertebral disc (IVD)Supercritical CO2 (scCO2)

Identifiers

PMID41904497
PMCPMC13151132

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.