# Surface Engineering of MXenes for Biomedical Uses: Functionalization Strategies and Application Trends

**Authors:** Sehyeon Park, Hee Jeong Byun, Jae Young Lee

PMC · DOI: 10.34133/bmr.0327 · Biomaterials Research · 2026-03-09

## TL;DR

This review discusses how modifying the surface of MXenes can improve their stability and usefulness in biomedical applications like tissue engineering and biosensing.

## Contribution

The paper categorizes MXene functionalization strategies and proposes design principles for next-generation biomedical platforms.

## Key findings

- Surface engineering enhances MXene biostability and biocompatibility.
- Functionalization enables MXenes to perform specific biomedical functions such as antibacterial therapy and bioimaging.
- The review categorizes strategies based on mechanisms and intended biomedical functions.

## Abstract

MXenes, a class of 2-dimensional transition metal carbides and nitrides, have emerged as highly versatile materials in the biomedical field because of their high electrical conductivity, hydrophilicity, large surface-area-to-mass ratio, and compositional versatility. Despite their promise, the inherent instability in physiological environments, lack of inherent biological activity, and potential toxicity remain major challenges limiting their biomedical applications. To address these issues, a wide range of surface engineering strategies have been developed, including covalent and noncovalent functionalization with various biomolecules, biomedical polymers, and nanomaterials. Specifically, the surface modification of MXene is intended to improve biostability and biocompatibility, and confer specific biological functions for applications in tissue engineering, biosensing, antibacterial therapy, and multimodal bioimaging. This review provides a comprehensive overview of the recent advances in MXene functionalization in the biomedical field. Based on their mechanisms and biomedical functions, we categorized the functionalization strategies and proposed key design principles for the development of next-generation MXene-based therapeutic and diagnostic platforms.

## Full-text entities

- **Genes:** Peroxidase [NCBI Gene 28379326]
- **Diseases:** CDT (MESH:C537067), infected (MESH:D007239), toxicities (MESH:D064420), corneal injury (MESH:D065306), CT (MESH:C000719218), osteomyelitis (MESH:D010019), cancer (MESH:D009369), diabetes (MESH:D003920), inflammation (MESH:D007249)
- **Chemicals:** nitrite (MESH:D009573), amino acid (MESH:D000596), Cr (MESH:D002857), CTAB (MESH:D000077286), Ti (MESH:D014025), poly(vinyl alcohol) (MESH:D011142), DTAB (MESH:C013912), thiol (MESH:D013438), polyester (MESH:D011091), Phe (MESH:D010649), amine (MESH:D000588), hydrofluoric acid (MESH:D006858), (3-mercaptopropyl)trimethoxysilane (MESH:C102833), Zr (MESH:D015040), Al (MESH:D000535), OTS (MESH:C061189), O-acylisourea (-), Si (MESH:D012825), superoxide (MESH:D013481), porphyrin (MESH:D011166), Graphene (MESH:D006108), H2O2 (MESH:D006861), 3-glycidoxypropyltrimethoxysilane (MESH:C403136), Bi (MESH:D001729), Pluronic F127 (MESH:D020442), DOX (MESH:D004317), Mo (MESH:D008982), hydrogen (MESH:D006859), MXene (MESH:C000723374), Trp (MESH:D014364), PNIPAM (MESH:C052970), dopamine (MESH:D004298), ethylenediamine (MESH:C031234), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (MESH:D005022), oxides (MESH:D010087), ROS (MESH:D017382), (3-(methacryloxy)propyltrimethoxysilane (MESH:C542237), PGA (MESH:D011454), dimethyl sulfoxide (MESH:D004121), Glucose (MESH:D005947), Mn (MESH:D008345), glycol (MESH:D006018), catechols (MESH:D002396), octyltriethoxysilane (MESH:C514699), GSH (MESH:D005978), TiO2 (MESH:C009495), polyphenol (MESH:D059808), Bi2S3 (MESH:C049897), OH (MESH:C031356), HAuCl4 (MESH:C024568), nitrogen (MESH:D009584), uric acid (MESH:D014527), His (MESH:D006639), PEG (MESH:D011092), MX (MESH:C054121), MOF (MESH:D000073396), polypyrrole (MESH:C067635), graphene oxide (MESH:C000628730), Ta (MESH:D013635), PAA (MESH:D010463)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090], Glycine max (soybean, species) [taxon 3847], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968399/full.md

## References

200 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968399/full.md

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Source: https://tomesphere.com/paper/PMC12968399