# Plasma-Assisted UV Grafting of Thermo-Responsive Chitosan-co-PNIPAAm Hydrogels on Polypropylene Nonwovens for Antibacterial Biomedical Textiles

**Authors:** Mei-Hsueh Nien, Yu-Qi Huang, Shu-Chuan Liao, Trong-Ming Don

PMC · DOI: 10.3390/polym18040479 · 2026-02-14

## TL;DR

Researchers developed a method to coat polypropylene nonwoven fabric with a temperature-sensitive and antibacterial hydrogel using plasma and UV techniques.

## Contribution

A scalable plasma-assisted UV grafting method to create thermo-responsive and antibacterial hydrogel coatings on polypropylene nonwovens.

## Key findings

- Plasma treatment and UV grafting successfully created a chitosan-co-PNIPAAm hydrogel on polypropylene nonwoven.
- The modified nonwoven showed thermo-responsive swelling and antibacterial activity against Escherichia coli.
- The hydrogel-coated fabric maintained good cytocompatibility with favorable cell viability.

## Abstract

Polypropylene (PP) nonwoven is widely used in biomedical textiles because of its lightweight and mechanical durability; however, its inherent hydrophobicity and chemical inertness limit further surface functionalization. In this study, a plasma-assisted UV grafting strategy was developed to fabricate thermo-responsive and antibacterial hydrogel coatings on PP nonwoven. Atmospheric-pressure plasma jet (APPJ) treatment was first employed to activate the PP nonwoven surface, followed by UV-induced graft polymerization of chitosan and N-isopropylacrylamide (NIPAAm), forming a chitosan-co-PNIPAAm hydrogel immobilized on the nonwoven substrate. Surface characterization using water contact angle measurement, Fourier transform infrared spectroscopy, and scanning electron microscopy confirmed effective plasma activation and successful hydrogel grafting. APPJ treatment significantly enhanced surface wettability, whereas subsequent UV grafting formed a continuous hydrogel on the PP nonwoven surface. The modified nonwoven exhibited distinct thermo-responsive swelling behavior in aqueous and simulated physiological environments, associated with the temperature-sensitive characteristics of the PNIPAAm component. In addition, the incorporation of chitosan imparted pronounced antibacterial activity against Escherichia coli, with inhibition zone diameters ranging from 14 to 16.5 mm, indicating high antibacterial sensitivity. Preliminary cytocompatibility evaluation further demonstrated favorable cell viability on the modified surfaces. This study demonstrates a scalable and low-temperature surface engineering approach for integrating stimuli-responsive and antibacterial hydrogel functionality into nonwoven polymer substrates, offering potential for advanced biomedical textile applications.

## Linked entities

- **Chemicals:** chitosan (PubChem CID 129662530), N-isopropylacrylamide (PubChem CID 16637)

## Full-text entities

- **Diseases:** pressure ulcers (MESH:D003668), cytotoxic (MESH:D064420), Infections (MESH:D007239), injury to (MESH:D014947), swelling (MESH:D004487)
- **Chemicals:** PP (MESH:D011126), OH (MESH:C031356), Alamar Blue (MESH:C005843), APS (MESH:D000250), N,N,N',N'-tetramethylethylenediamine (MESH:C005798), CO2 (MESH:D002245), ammonium persulfate (MESH:C031276), Argon (MESH:D001128), -PNIPAAm (MESH:C052970), RNS (MESH:D011886), N,N'-methylenebisacrylamide (MESH:C021221), penicillin (MESH:D010406), C6H16N2 (-), Vitamin B2 (MESH:D012256), amphotericin (MESH:D000666), resorufin (MESH:C014180), Water (MESH:D014867), amide (MESH:D000577), ethanol (MESH:D000431), NMBA (MESH:C468271), acetic acid (MESH:D019342), CS (MESH:D048271), O (MESH:D010100), platinum (MESH:D010984), -NIPAAm (MESH:C067295), agar (MESH:D000362), chitin (MESH:D002686), polymer (MESH:D011108), C (MESH:D002244), streptomycin (MESH:D013307), polysaccharide (MESH:D011134), Nitrogen (MESH:D009584)
- **Species:** Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** NIH-3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594), NIH-3T3 fibroblasts — Mus musculus (Mouse), Transformed cell line (CVCL_L992), ATCC 25922 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943827/full.md

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Source: https://tomesphere.com/paper/PMC12943827