# Patient-specific 3D cryo(bio)printing of a glenoid labrum scaffold for fibrocartilaginous tissue engineering

**Authors:** Francklin Trindade da Silva, Caio Moreira de Souza, Thiago Domingues Stocco

PMC · DOI: 10.3389/fbioe.2026.1758582 · Frontiers in Bioengineering and Biotechnology · 2026-02-05

## TL;DR

Researchers developed a 3D-printed scaffold for the glenoid labrum using patient-specific models and cryo(bio)printing, showing improved precision and cell viability.

## Contribution

This is the first demonstration of bioprinting a patient-specific glenoid labrum scaffold using cryo(bio)printing and GelMA hydrogel.

## Key findings

- Cryogenic printing improved structural fidelity and reduced filament spreading in scaffold fabrication.
- Bioprinted scaffolds at −20°C showed the highest anatomical accuracy when compared to digital models.
- Human mesenchymal stem cells remained viable under all tested temperature conditions.

## Abstract

The glenoid labrum is a fibrocartilaginous structure essential for shoulder stability, yet its regeneration remains an unmet clinical challenge. Current surgical approaches restore initial joint stability but frequently fail to reestablish native biomechanics, leading to recurrence and early degenerative changes. In this study, we investigated the feasibility of fabricating a patient-specific, anatomically scaled glenoid labrum scaffold using digital modeling based on magnetic resonance imaging and 3D cryo(bio)printing of a gelatin methacryloyl (GelMA) hydrogel. Printing was performed in a temperature-controlled platform (22.5 °C, 15 °C, and −20 °C) to evaluate the influence of thermal conditions on structural fidelity and biological performance. Quantitative analyses showed that cryogenic deposition markedly improved printing precision, reducing filament spreading and enhancing geometric accuracy in both sharp-angle and grid-pattern evaluations. Biological assays indicated high viability of human mesenchymal stem cells under all temperature conditions, validating the cytocompatibility of the methodology. Morphological assessment by structured-light 3D scanning demonstrated that bioprinted patient-specific scaffold at −20 °C achieved the highest correspondence to the digital reference model. Overall, the integration of anatomical modeling with cryo(bio)printing proved to be an effective approach for producing anatomically faithful, patient-tailored scaffolds. This study presents the first demonstration of human glenoid labrum bioprinting and establishes a foundation for future translational research in fibrocartilaginous tissue regeneration.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** synovitis (MESH:D013585), neurological injury (MESH:D020196), dislocations (MESH:D004204), post-instability arthropathy (MESH:D043171), Bankart (MESH:D000070896), trauma (MESH:D014947), degenerative (MESH:D019636), pain (MESH:D010146), glenohumeral osteoarthritis (MESH:D010003), Glenoid labrum injuries (MESH:D000070599), cartilage degeneration (MESH:D002357), anterior shoulder dislocations (MESH:D012783)
- **Chemicals:** D-(+)-melezitose hydrate (-), graphene (MESH:D006108), EthD-1 (MESH:C018533), PBS (MESH:D007854), Lithium phenyl-2,4,6-trimethylbenzoylphosphinate (MESH:C546776), DMSO (MESH:D004121), ice (MESH:D007053), L-glutamine (MESH:D005973), CO2 (MESH:D002245), EDTA (MESH:D004492), calcein-AM (MESH:C085925), Melezitose (MESH:C005190), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916613/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916613/full.md

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Source: https://tomesphere.com/paper/PMC12916613