journal article·2026-07-01

Core–Shell Nanoparticle Additive Enables High-Efficacy Antimicrobial Coatings

Ricardo Ortega, Zhengtao Yang, Serkan Demirci, Tiago A Twedt, Utsav Kumar Dey, Fei Liu, Thamer Sabri M Rawah, Nubia Resende De Macedo, Juan-Carlos Mora-Diaz, Luis G. Gimenez-Lirola, Shan Jiang

ACS Applied Materials & Interfaces· Volume 18· Issue 25
Publisher page

Abstract

Microbial proliferation on surfaces poses a persistent challenge for applications requiring hygienic or sterile environments. Hydantoin-based antimicrobials are attractive N -halamine precursors because of their rapid biocidal activity, low toxicity, and long-lasting functionality. Hydantoin-based monomers, such as hydantoin acrylamide (HA), have previously been used to synthesize copolymers with potent antimicrobial properties. However, their practical application in waterborne coatings is limited by the high cost and poor aqueous solubility of HAs. Here, a core–shell (CS) particle architecture consisting of a polystyrene core and a poly(hydantoin acrylamide) (PHA) shell is reported to address these limitations. This design reduces HA usage by approximately 65% while preserving antimicrobial performance, resulting in nearly 3-fold reduction in material costs. In addition, the CS particles exhibit an 18-fold increase in solid loadings and 20–35% smaller particle sizes compared with pure PHA particles. Upon activation with dilute chlorine bleach (20–100 ppm), antimicrobial N -halamines were successfully generated on the particle surface, with CS particles showing approximately 10% higher oxidative chlorine levels compared to pure PHA particles dispersed in aqueous suspension. When incorporated into waterborne coatings, the CS particles enabled fully rechargeable antimicrobial films with high efficacy. Dried coating films could be recharged by using a simple bleach treatment over at least five recharge cycles. Contact killing experiments against Staphylococcus aureus and Escherichia coli demonstrated 100% bacterial killing within 30 min at 3% additive loading. Overall, our CS approach establishes an efficient and scalable route for producing durable antimicrobial additives that can be readily integrated into waterborne coating systems without modification of primary film chemistry.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Bone Tissue Engineering Materials · Electrophoretic Deposition in Materials Science · Polymer Surface Interaction Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science and Engineering

Iowa State University of Science and Technology

Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine

Iowa State University

Funding

National Science Foundation · 3M Non-Tenured Faculty Award · Innovation Acceleration Fund provided by the Iowa Board of Regents and State Economic Development and Industry Relations (EDIR) · Department of Defense SERDP program

References (41)

Show source-provided references
1. WHO. Food safety. World Health Organization ; 2024. https://www.who.int/news-room/fact-sheets/detail/food-safety. (accessed 2026 1/19/2026).
2. 10.3390/polym1506158610.3390/polym15061586 ↗
3. 10.1021/acsami.9b1781510.1021/acsami.9b17815 ↗
4. 10.1002/advs.20210604910.1002/advs.202106049 ↗
5. 10.1039/C5RA03881B10.1039/C5RA03881B ↗
6. 10.1039/C7NJ02023F10.1039/C7NJ02023F ↗
7. 10.1021/acs.est.2c0824410.1021/acs.est.2c08244 ↗
8. 10.1128/cmr.00181-1910.1128/cmr.00181-19 ↗
9. 10.1021/acs.chemrev.6b0068710.1021/acs.chemrev.6b00687 ↗
10. 10.1021/nn507168x10.1021/nn507168x ↗
11. 10.1002/app.4482110.1002/app.44821 ↗
12. 10.1016/S0015-1882(10)70075-610.1016/S0015-1882(10)70075-6 ↗
13. 10.1002/mabi.20180045310.1002/mabi.201800453 ↗
14. 10.1002/adfm.20230728610.1002/adfm.202307286 ↗
15. 10.1002/adfm.20210347710.1002/adfm.202103477 ↗
16. 10.1016/j.biomaterials.2014.02.05610.1016/j.biomaterials.2014.02.056 ↗
17. 10.1016/j.reactfunctpolym.2012.06.01810.1016/j.reactfunctpolym.2012.06.018 ↗
18. 10.3390/polym1308126910.3390/polym13081269 ↗
19. 10.1021/am200684u10.1021/am200684u ↗
20. 10.1002/slct.20220228510.1002/slct.202202285 ↗
21. 10.1021/jp104083h10.1021/jp104083h ↗
22. 10.1016/j.colsurfb.2016.09.03010.1016/j.colsurfb.2016.09.030 ↗
23. 10.1016/j.colsurfb.2013.09.04810.1016/j.colsurfb.2013.09.048 ↗
24. 10.1016/j.jcis.2013.09.03610.1016/j.jcis.2013.09.036 ↗
25. 10.1039/C4NJ01806K10.1039/C4NJ01806K ↗
26. 10.1002/app.2777410.1002/app.27774 ↗
27. 10.1021/acs.biomac.0c0076910.1021/acs.biomac.0c00769 ↗
28. 10.1002/marc.20210056610.1002/marc.202100566 ↗
29. 10.1016/j.coesh.2026.10070610.1016/j.coesh.2026.100706 ↗
30. 10.1021/acsabm.3c0124710.1021/acsabm.3c01247 ↗
31. 10.1021/acsami.9b0346410.1021/acsami.9b03464 ↗
32. 10.1021/acs.jafc.8b0386410.1021/acs.jafc.8b03864 ↗
33. 10.1016/j.actbio.2011.12.02710.1016/j.actbio.2011.12.027 ↗
34. 10.1016/j.vetmic.2018.03.03210.1016/j.vetmic.2018.03.032 ↗
35. 10.1016/j.mimet.2020.10593710.1016/j.mimet.2020.105937 ↗
36. 10.1016/j.cej.2014.05.11410.1016/j.cej.2014.05.114 ↗
37. 10.3390/molecules2903064110.3390/molecules29030641 ↗
38. 10.1002/jbm.a.3146310.1002/jbm.a.31463 ↗
39. 10.1039/d0mh00589d10.1039/d0mh00589d ↗
40. 10.2352/ISSN.2169-4451.2012.28.1.art00039_210.2352/ISSN.2169-4451.2012.28.1.art00039_2 ↗
41. 10.1016/j.bioflm.2022.10007610.1016/j.bioflm.2022.100076 ↗