# Dual-functional sulfonated PEEK implants via graphene oxide–mediated BMP-2 gene delivery: enhanced osteogenic and antibacterial performance in vitro

**Authors:** Yueying Pan, Bumairemu Yiminjiang, Adilai Abula, Refeina Tuerxun, Maihefuzi Aishan

PMC · DOI: 10.3389/fmed.2026.1763692 · Frontiers in Medicine · 2026-03-04

## TL;DR

A new PEEK implant was developed that promotes bone growth and fights bacteria using graphene oxide and BMP-2 gene delivery.

## Contribution

A dual-functional PEEK implant was created with BMP-2 gene delivery and antibacterial properties via GO-based coatings.

## Key findings

- The SPEEK-(GO-PEG/pBMP-2) composite significantly improved osteoblast adhesion, proliferation, and mineralization.
- GO-containing coatings showed strong antibacterial activity against both Gram-positive and Gram-negative bacteria.
- PEGylation of GO and pBMP-2 loading were confirmed to be efficient and uniform.

## Abstract

Polyetheretherketone (PEEK) is a promising orthopedic implant material due to its bone-mimetic mechanical properties; however, its bioinert surface and susceptibility to bacterial colonization limit its clinical efficacy. Strategies to enhance osteointegration while providing antibacterial functionality are urgently needed.

Graphene oxide (GO) was functionalized with polyethylene glycol (PEG) and complexed with a plasmid encoding bone morphogenetic protein-2 (pBMP-2) to form a GO-PEG/pBMP-2 complex. This complex was coated onto sulfonated PEEK (SPEEK) via freeze-drying, yielding SPEEK-(GO-PEG/pBMP-2) composites. The materials were systematically compared with pristine PEEK, SPEEK, and SPEEK-GO-PEG controls. Surface chemistry, morphology, hydrophilicity, gene loading efficiency, and coating uniformity were characterized. In vitro assessments included cell adhesion, proliferation, viability, alkaline phosphatase (ALP) activity, mineralized matrix deposition, osteogenic gene expression, and antibacterial activity against Staphylococcus aureus and Escherichia coli.

Successful PEGylation of GO and efficient pBMP-2 loading were confirmed, with uniform coating and significantly improved hydrophilicity on SPEEK-(GO-PEG/pBMP-2). This composite markedly enhanced osteoblast adhesion, proliferation, and viability, along with elevated ALP activity, increased mineralized nodule formation, and upregulated expression of key osteogenic genes (e.g., Runx2, OPN, OCN). Both GO-containing coatings—SPEEK-GO-PEG and SPEEK-(GO-PEG/pBMP-2)—exhibited strong antibacterial effects against both Gram-positive and Gram-negative bacteria, with no significant difference attributable to BMP-2 loading.

The SPEEK-(GO-PEG/pBMP-2) platform simultaneously promotes osteogenesis through localized BMP-2 gene delivery and provides robust antibacterial protection via GO. This dual-functional design addresses two major limitations of PEEK implants, offering a promising strategy for next-generation orthopedic biomaterials.

## Linked entities

- **Genes:** RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860], SPP1 (secreted phosphoprotein 1) [NCBI Gene 6696], BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632]
- **Proteins:** BMP2 (bone morphogenetic protein 2)
- **Chemicals:** polyethylene glycol (PubChem CID 9033), alkaline phosphatase (PubChem CID 18985873)
- **Species:** Staphylococcus aureus (taxon 1280), Escherichia coli (taxon 562)

## Full-text entities

- **Chemicals:** PEEK (MESH:C063834), PEG (MESH:D011092), GO-PEG (-), GO (MESH:C000628730)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12996093/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996093/full.md

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Source: https://tomesphere.com/paper/PMC12996093