Evidence map›Paper›PMID 42261426›Full record

ArticleIndian journal of orthopaedics2026

3D-Printed Antibiotic Beads with Controlled Microarchitectures for Customizable Elution Profiles: An In Vitro Study.

Vivek K Bilolikar, Duncan Van Vannest, Clark Chen, Solomon P Samuel, John A Handal, James S Raphael

Abstract read
In one paragraph

Article in Indian journal of orthopaedics, 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

6 authors.

Vivek K BilolikarDepartment of Orthopaedics, Jefferson Einstein Philadelphia Hospital - Jefferson Health, 5501 Old York Rd, WCB4, Philadelphia, PA 19141 USA.ORCID 0000-0001-6818-4705
Duncan Van VannestDepartment of Orthopaedics, Jefferson Einstein Philadelphia Hospital - Jefferson Health, 5501 Old York Rd, WCB4, Philadelphia, PA 19141 USA.
Clark ChenDepartment of Orthopaedics, Jefferson Einstein Philadelphia Hospital - Jefferson Health, 5501 Old York Rd, WCB4, Philadelphia, PA 19141 USA.
Solomon P SamuelDepartment of Orthopaedics, Jefferson Einstein Philadelphia Hospital - Jefferson Health, 5501 Old York Rd, WCB4, Philadelphia, PA 19141 USA.
John A HandalDepartment of Orthopaedics, Jefferson Einstein Philadelphia Hospital - Jefferson Health, 5501 Old York Rd, WCB4, Philadelphia, PA 19141 USA.
James S RaphaelDepartment of Orthopaedics, Jefferson Einstein Philadelphia Hospital - Jefferson Health, 5501 Old York Rd, WCB4, Philadelphia, PA 19141 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Polymethylmethacrylate (PMMA) antibiotic beads are widely used in orthopedic surgery for localized infection control, but inconsistent drug elution can limit efficacy. Three-dimensional (3D) printing offers a way to create implants with controlled architectures, enabling more predictable and customizable drug release. This study explores the use of internal structural variation to influence the elution profiles of vancomycin and tetracycline and assess their antibacterial properties. Methods: Cylindrical specimens were 3D printed using a commercial resin mixed with 2% vancomycin or tetracycline. To evaluate the effects of composition and structure, additives such as sodium chloride (NaCl) and polyvinylpyrrolidone (PVP) were included, and four internal architectures-solid, hollow, large honeycomb, and small honeycomb-were tested. Elution was assessed over 7 days, and antibacterial activity was tested against Results: Tetracycline exhibited greater cumulative release than vancomycin, likely due to solubility and molecular weight differences. Honeycomb structures, especially the smaller variant, produced the most sustained and consistent elution profiles. NaCl decreased vancomycin but increased tetracycline release, while PVP enhanced release for both. All formulations showed antibacterial efficacy. Discussion: 3D printing enables the design of antibiotic-eluting implants with tailored release profiles. The honeycomb architecture is especially promising for sustained delivery. Further in vivo studies are needed to confirm clinical relevance and optimize formulations for orthopedic use.

Indexed as

3D printingAntibioticsBone cementCADCustomized drug deliveryInfection managementOsteomyelitisPorogenProsthetic joint infection

Identifiers

PMID42261426
PMCPMC13242312

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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.