Evidence map›Paper›PMID 42783689›Full record

ArticleJournal of functional biomaterials2026

Enhanced Osteoinduction, Rheological and Mechanical Performance of 3D-Printed Methylcellulose-Gelatin-Hydroxyapatite Scaffolds.

Ceren Yuksel, Simon Kwoon-Ho Chow, Ryota Hirose, Mayu Morita, Qi Gao, Takahiro Igei, Monica Thukkaram, Chao Ma, Tony Tam, Sophie Clarke and 3 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Ceren YukselInstitute of Biomedical Engineering, Boğaziçi University, Istanbul 34684, Türkiye.
Simon Kwoon-Ho ChowDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-1742-980X
Ryota HiroseDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0009-0002-3357-1304
Mayu MoritaDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
Qi GaoDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-0175-566X
Takahiro IgeiDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
Monica ThukkaramDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
Chao MaDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-1049-6172
Tony TamDepartment of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-0288-5434
Sophie ClarkeDepartment of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.
Mark Skylar ScottDepartment of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.
Stuart GoodmanDepartment of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-1919-3717
Duygu EgeInstitute of Biomedical Engineering, Boğaziçi University, Istanbul 34684, Türkiye.ORCID 0000-0002-9922-6995

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex patient-specific bone defects remain difficult to reconstruct because the regenerative capacity of bone is limited and prefabricated implants cannot readily match defect geometry. In this work, methylcellulose-gelatin-hydroxyapatite (MC/GEL/HA) inks were formulated with varying methylcellulose content and hydroxyapatite incorporation, crosslinked with EDC/NHS, and 3D-printed into porous scaffolds with defined square-pore architectures. Inks were evaluated by oscillatory and steady-shear rheology, and printed scaffolds were characterized for morphology, chemical composition, mechanical performance, physicochemical stability, wettability, apatite-forming bioactivity, and osteogenic responses of human bone marrow mesenchymal stem cells. Methylcellulose content primarily governed ink rheology and printability, and increased compressive strength (up to ~0.38 MPa for 15MC/10GEL/30HA), whereas hydroxyapatite enhanced surface hydrophilicity, promoted apatite nucleation within 7 days in simulated body fluid, and markedly increased alkaline phosphatase activity (>10-fold over HA-free scaffolds), mineralization (~2-fold by Alizarin Red), and the highest osteocalcin expression among the HA-containing formulations (~2.45-fold at day 14). The 15MC/10GEL/30HA formulation showed the most favorable balance of printability, mechanical performance, and osteogenic performance. These complementary functions reconciled structural stability with osteogenic performance, supporting the MC/GEL/HA system as a tunable bioink platform for non-weight-bearing bone regeneration, while warranting further in vivo validation.

Indexed as

3D printingbone tissue engineeringgelatinhydroxyapatitemethylcelluloseosteogenic differentiation

Identifiers

PMID42783689
PMCPMC13607947

What OpenQuestion holds

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Registered trials

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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.