# Antimicrobial 3D printed implants for periprosthetic joint infections

**Authors:** Iván Yuste, Francis C. Luciano, Carmina Rodríguez, Bianca I. Ramirez, Chrysi Rapti, Brayan J. Anaya, Aikaterini Lalatsa, Almudena Ribed-Sánchez, Pablo Sanz-Ruiz, Elena González-Burgos, Dolores R. Serrano

PMC · DOI: 10.1007/s13346-025-01934-5 · Drug Delivery and Translational Research · 2025-08-14

## TL;DR

This paper introduces 3D-printed implants that release antibiotics to prevent joint infections after surgery.

## Contribution

A novel 3D-printed implant is developed for targeted antimicrobial delivery to prevent periprosthetic joint infections.

## Key findings

- The implants show broad-spectrum antimicrobial activity against Candida and Staphylococcus species.
- Amphotericin B exhibits sustained release and reduced hemolytic toxicity compared to free drug.
- The implants adhere to prosthetic surfaces rapidly and maintain drug solubility for 48 hours.

## Abstract

Periprosthetic joint infections (PJIs) remain a serious complication following hip and knee arthroplasty, affecting 1–5% of patients in developed countries and posing significant challenges to patients, clinicians, and healthcare systems. Conventional prophylactic strategies, such as antibiotic-loaded bone cement, suffer from limited post-implantation drug release and potential compromise of mechanical integrity. To overcome these limitations, we developed a personalized, 3D-printed implant designed to integrate with the acetabular component of joint prostheses. These implants deliver either monotherapy or a combination of amphotericin B (AmB) and vancomycin (VAN), targeting both fungal and bacterial pathogens. Fabricated via fused deposition modeling using a biocompatible polyvinyl alcohol–polyethylene glycol (PVA–PEG) matrix, the implants enable passive drug loading and rapid adhesion to prosthetic surfaces within 60 s, minimizing operative time. In vitro testing confirmed broad-spectrum antimicrobial activity against Candida spp. (C. albicans, C. parapsilosis, C. glabrata, C. krusei) and Staphylococcus spp. (S. aureus, S. epidermidis). VAN was released rapidly, while AmB exhibited sustained release for up to 10 h, with both maintaining saturation solubility for 48 h. Notably, AmB-loaded implants showed five-fold lower hemolytic toxicity compared to free drug. These results highlight the potential of 3D-printed, drug-eluting implants as a clinically viable solution for the prevention and early treatment of PJIs.

The online version contains supplementary material available at 10.1007/s13346-025-01934-5.

## Linked entities

- **Chemicals:** amphotericin B (PubChem CID 1972), vancomycin (PubChem CID 14969)
- **Species:** Candida albicans (taxon 5476), Staphylococcus aureus (taxon 1280), Staphylococcus epidermidis (taxon 1282)

## Full-text entities

- **Diseases:** PJIs (MESH:D057068), hemolytic toxicity (MESH:D064420)
- **Chemicals:** PVA-PEG (-), AmB (MESH:D000666), VAN (MESH:D014640)
- **Species:** Candida albicans (species) [taxon 5476], Staphylococcus epidermidis (species) [taxon 1282], Lodderomyces parapsilosis (species) [taxon 5480], Pichia kudriavzevii (species) [taxon 4909], Homo sapiens (human, species) [taxon 9606], Candida [taxon 1535326], Nakaseomyces glabratus (species) [taxon 5478]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13038732/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038732/full.md

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Source: https://tomesphere.com/paper/PMC13038732