# Smart Antibiofilm Platforms Based on Synthetic Antimicrobial Peptides-Engineered Hydrogels

**Authors:** Carpa Rahela, Bogyor Agota-Katalin, Butiuc-Keul Anca

PMC · DOI: 10.3390/polym18040471 · Polymers · 2026-02-12

## TL;DR

This paper reviews smart hydrogel platforms engineered with synthetic antimicrobial peptides to combat biofilm infections in chronic wounds and medical devices.

## Contribution

The paper introduces novel strategies for peptide engineering and hydrogel integration to enhance antibiofilm therapies.

## Key findings

- Synthetic AMPs offer advantages like tunable sequences and functional modifications for improved antibiofilm activity.
- Hydrogels enable localized AMP delivery, sustained release, and support tissue repair through multifunctional properties.
- Challenges include peptide stability, manufacturing costs, and regulatory barriers for clinical translation.

## Abstract

Chronic wounds and implanted medical devices remain highly vulnerable to biofilm-associated infections, which resist conventional antibiotics and immune clearance. Synthetic antimicrobial peptides (AMPs) have emerged as promising alternatives, offering tunable sequences, short lengths for cost-effective synthesis, and functional modifications that enhance stability and antibiofilm potency. Hydrogels provide an optimal delivery matrix by enabling localized AMP release, maintaining a moist wound environment, and supporting stimuli-responsive or sustained therapeutic action. This review highlights recent advances in peptide engineering strategies—including rational sequence design, chemical modifications, and self-assembling nanostructures—alongside hydrogel integration approaches ranging from physical entrapment to covalent tethering and infection-triggered release systems. Mechanistic insights into antibiofilm activity are discussed, supported by in vitro, ex vivo, and in vivo evaluation models. Beyond antimicrobial efficacy, multifunctional AMP–hydrogel systems can deliver complementary benefits such as hemostasis, anti-inflammation, or enzymatic biofilm dispersal, further accelerating tissue repair. Despite significant progress, translational challenges remain, including peptide stability, manufacturing costs, regulatory hurdles, and host safety. Future directions point toward AI-driven peptide design, programmable hydrogels, and point-of-care integration to realize safe, effective, and multifunctional AMP–hydrogel therapies for chronic wound management and biofilm eradication.

## Full-text entities

- **Genes:** Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Egf (epidermal growth factor) [NCBI Gene 13645]
- **Diseases:** adhesions (MESH:D000267), catheter (MESH:D055499), pressure sores (MESH:D003668), diabetic foot ulcers (MESH:D017719), cytotoxicity (MESH:D064420), wound infections (MESH:D014946), bone infections (MESH:D001847), biofilm infections (MESH:D007239), blood coagulation (MESH:D001778), associated (MESH:D018886), osteomyelitis (MESH:D010019), orthopedic infections (MESH:D009140), bacterial infections (MESH:D001424), MRSA (MESH:D013203), fungal infections (MESH:D009181), sinusitis (MESH:D012852), inflammation (MESH:D007249), Chronic wounds (MESH:D014947), , skin, ear, nose and throat, (MESH:D004427), diabetic (MESH:D003920), lung, bladder, wound (MESH:D008171), venous ulcers (MESH:D014647), hemolysis (MESH:D006461)
- **Chemicals:** Bi (MESH:D001729), PFKLSLHL-NH2 (MESH:C495931), Ac-RKKWFW-NH2 (MESH:C459185), dextran (MESH:D003911), CV (MESH:D005840), FKF (-), polyvinyl chloride (MESH:D011143), Arg (MESH:D001120), fatty-acid (MESH:D005227), hydrocarbon (MESH:D006838), MTT (MESH:C070243), amino acids (MESH:D000596), ergosterol (MESH:D004875), titanium (MESH:D014025), resorufin (MESH:C014180), lipid (MESH:D008055), adamantane (MESH:D000218), palmitic acid (MESH:D019308), polystyrene (MESH:D011137), lipopeptide (MESH:D055666), resazurin (MESH:C005843), RA (MESH:D011883), BR (MESH:D001599), ROS (MESH:D017382), hydrogen (MESH:D006859), Trp (MESH:D014364), dopamine (MESH:D004298), guanosine tetraphosphate (MESH:D006159), PNIPAM (MESH:C052970), PBS (MESH:D007854), sphingolipids (MESH:D013107), Lys (MESH:D008239), formazan (MESH:D005562), thioether (MESH:D013440), alginate (MESH:D000464), chitosan (MESH:D048271), phosphatidylinositol (MESH:D010716), salts (MESH:D012492), AMP (MESH:D000089882), acid (MESH:D000143), gold (MESH:D006046), acrylic acid (MESH:C036658), EPS (MESH:C100219), polyacrylamide (MESH:C016679), polymer (MESH:D011108), agar (MESH:D000362), ADP (MESH:D000244), J1 (MESH:C072665), PEG (MESH:D011092), polysaccharides (MESH:D011134), CAZ (MESH:D002442), Peptide (MESH:D010455), cerium oxide (MESH:C030583), Methylcellulose (MESH:D008747), glucosylceramides (MESH:D005963), phospholipid (MESH:D010743), water (MESH:D014867), tetrazolium (MESH:D013778), amide (MESH:D000577), HA (MESH:D006820)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116], Acinetobacter baumannii (species) [taxon 470], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Escherichia coli (E. coli, species) [taxon 562], Candida albicans (species) [taxon 5476], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** M33D, Lys/Arg
- **Cell lines:** fibroblasts — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594)

## Full text

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## Figures

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## References

153 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944519/full.md

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Source: https://tomesphere.com/paper/PMC12944519