ArticleACS omega2025
Process-Driven Optimization of FDM Porous PEEK Scaffolds for Alloplastic Bone Grafts.
Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Fabrication and Characterization of a Porous TiOACS biomaterials science & engineering · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Polyether ether ketone (PEEK) has emerged as a high-performance biomaterial for orthopedic and craniofacial applications due to its exceptional mechanical properties, chemical stability, and biocompatibility. Despite its clinical potential, the additive manufacturing of PEEK, particularly through fused deposition modeling (FDM), remains a considerable technical challenge owing to the polymer's high melting point and narrow processing window. In this study, we report a novel and practical strategy for producing porous PEEK scaffolds with an optimized architecture suitable for bone graft applications. All initial CAD-based lattice designs failed under FDM processing conditions, consistently resulting in misprints with poor fidelity and structural inconsistencies. To address this, a process-driven approach through the adjustment of slicing parameters was adapted. Through iterative optimization, a reproducible scaffold design was achieved, with interconnected porosity and pore dimensions ranging from 100 to 400 μm, within the ideal range to support osteoblast adhesion, proliferation, and vascularization. The resulting scaffolds exhibited consistent morphology, mechanical integrity, and geometric fidelity, showing the importance of the slicing software parameters when used to circumvent computer-aided design limitations. This work demonstrates the pivotal role of manipulating the slicing software to unlock the full potential of high-performance thermoplastics such as PEEK in bone tissue engineering. Our findings offer a scalable pathway for producing customized, load-sharing scaffolds and open new avenues for integrating advanced manufacturing strategies in regenerative medicine.
Identifiers
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Registered trials
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.