# 3D Printing of Bacteriophage‐Loaded Hydrogels: Development of a Local and Long‐Lasting Delivery System

**Authors:** Corina Vater, Gopala Krishna Mannala, Max von Witzleben, Richard Frank Richter, Nike Walter, Michael Gelinsky, Volker Alt, Anja Lode, Markus Rupp

PMC · DOI: 10.1002/adhm.202503113 · Advanced Healthcare Materials · 2025-10-13

## TL;DR

This paper explores using 3D-printed hydrogels to deliver bacteriophages for treating drug-resistant bacterial infections near implants.

## Contribution

A novel 3D-printable hydrogel system is developed for sustained local delivery of active bacteriophages over 35 days.

## Key findings

- Bacteriophage-loaded AlgMC hydrogels maintain shape fidelity after 3D printing.
- Active bacteriophages are released for up to 35 days in a human-plasma-like medium.
- Adding Laponite does not extend release under physiological conditions but may protect phages in harsh environments.

## Abstract

Multiple drug‐resistant bacteria are a growing life‐threatening problem and novel treatment strategies are urgently needed. One promising option is the use of lytic bacteriophages, viruses that infect and kill bacteria with high specificity. To efficiently utilize bacteriophage therapy for the treatment of implant‐associated infections, an effective strategy for the local, long‐lasting administration of bacteriophages at the site of infection is required. With the aim of developing a defined delivery system, this study investigates the feasibility of 3D extrusion printing of bacteriophages embedded in biomaterial inks by using a Staphylococcus aureus‐specific phage strain as model. It is demonstrated that a bacteriophage‐loaded hydrogel blend consisting of alginate and methylcellulose (AlgMC) can be printed with high shape fidelity. After cross‐linking, the hydrogel constructs release bacteriophages that maintain their activity against S. aureus over a period of 35 days when incubated in human‐plasma‐like medium (HPLM). The integration of the nanoclay Laponite into the AlgMC blend, known for its high binding capacity for biomolecules, does not further prolong the release under (near) physiological conditions in HPLM but may protect bacteriophages under nonphysiological conditions. In conclusion, bacteriophage‐loaded AlgMC inks fulfill the requirements for local bacteriophage therapy as they release active bacteriophages in a sustained manner.

This research investigates the feasibility of 3D‐printing of a bacteriophage‐containing hydrogel made of alginate and methylcellulose. The printed hydrogels steadily release active bacteriophages for up to 35 days which is beneficial to treat implant‐associated infections. Although adding the nanoclay Laponite does not prolong the release under physiological conditions, it may be advantageous in harsher environments.

## Linked entities

- **Chemicals:** alginate (PubChem CID 5102882), Laponite (PubChem CID 71587168)
- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** infection (MESH:D007239)
- **Chemicals:** methylcellulose (MESH:D008747), Laponite (MESH:C524813), alginate (MESH:D000464), AlgMC (-)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Bacteriophage sp. (species) [taxon 38018], Staphylococcus aureus (species) [taxon 1280], 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/PMC12864588/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864588/full.md

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Source: https://tomesphere.com/paper/PMC12864588