journal article·2026-03-13

Multifunctional Polytetrahydropyrimidines with Potent Antimicrobial and Antioxidant Effects for Psoriasis Therapy

Hao Zhao, Chunxiao Li, Xiaohua Li, Shengjie Zhang, Yayun Zhu, Vellingiri Yasothamani, Hailin Cong, Bing Yu, Ge Yang

ACS Applied Polymer Materials· Volume 8· Issue 5
Publisher page

Abstract

Psoriasis is a chronic, immune-mediated inflammatory skin disease marked by recurrent lesions, which severely impact the quality of life of patients. While conventional treatments such as topical corticosteroids and immunosuppressants can relieve symptoms, prolonged use frequently leads to adverse effects, including skin irritation, liver toxicity, and bacterial infections. The colonization of S. aureus and its exotoxins play a key role in psoriasis pathogenesis, complicating treatment. Thus, controlling bacterial infections and toxin production is critical for improving therapeutic outcomes. In response to concerns over bacterial resistance, pyrimidine derivatives have gained significant attention due to their antibacterial, anti-inflammatory, and immunomodulatory properties. This study synthesized a series of poly tetrahydropyrimidine (PTHP) derivatives with various functional groups and backbone structures, identifying P-T-3 as the most promising candidate with excellent antimicrobial, anti-inflammatory, and biocompatible properties. Results show that P-T-3 effectively eliminates S. aureus and reduces toxin production, alleviating recurrent infections. Additionally, P-T-3 demonstrates antioxidant and anti-inflammatory effects, scavenging free radicals and reducing oxidative stress damage, enhancing psoriasis treatment. It also offers potential protection for patients on long-term immunosuppressive therapy. This presents a promising therapeutic approach for psoriasis, with the potential to enhance clinical outcomes and reduce the risk of complications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Psoriasis: Treatment and Pathogenesis · Multicomponent Synthesis of Heterocycles · Antimicrobial agents and applications

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

Affiliations

College of Chemistry and Chemical Engineering, College of Materials Science and Engineering, Institute of Biomedical Materials and Engineering

Qingdao University

School of Materials Science and Engineering

Shandong University of Technology

College of Chemistry, Chemical Engineering and Materials Science

Zaozhuang University

State Key Laboratory of Bio-Fibers and Eco-Textiles

Funding

National Key Research and Development Program of China · State Key Laboratory of Bio-Fibers and Eco-Textiles · National Natural Science Foundation of China · Natural Science Foundation of Shandong Province · Medical Plus Key Project of Qingdao University · Science and Technology Planing Project of South District of Qingdao City

References (46)

Show source-provided references
1. 10.1016/S0140-6736(20)32549-610.1016/S0140-6736(20)32549-6 ↗
2. 10.1192/j.eurpsy.2025.112310.1192/j.eurpsy.2025.1123 ↗
3. 10.1111/jdv.1974010.1111/jdv.19740 ↗
4. 10.3390/ijms22211157410.3390/ijms222111574 ↗
5. 10.1007/s13555-016-0117-610.1007/s13555-016-0117-6 ↗
6. 10.1111/ddg.1504210.1111/ddg.15042 ↗
7. 10.7717/peerj.1932510.7717/peerj.19325 ↗
8. 10.2147/CCID.S54040710.2147/CCID.S540407 ↗
9. 10.4161/derm.1753410.4161/derm.17534 ↗
10. 10.1159/00025202010.1159/000252020 ↗
11. 10.1046/j.1365-2230.2002.00998.x10.1046/j.1365-2230.2002.00998.x ↗
12. 10.1007/s00210-025-04334-110.1007/s00210-025-04334-1 ↗
13. 10.1111/1346-8138.1724510.1111/1346-8138.17245 ↗
14. 10.1111/myc.7008110.1111/myc.70081 ↗
15. 10.1111/j.1600-0625.2011.01322.x10.1111/j.1600-0625.2011.01322.x ↗
16. 10.3390/antibiotics1111150410.3390/antibiotics11111504 ↗
17. 10.1111/pde.1600710.1111/pde.16007 ↗
18. 10.3390/ijms2313695510.3390/ijms23136955 ↗
19. 10.1684/ejd.2009.066310.1684/ejd.2009.0663 ↗
20. 10.1046/j.1365-2230.2000.00575.x10.1046/j.1365-2230.2000.00575.x ↗
21. 10.1016/j.bmcl.2018.06.04910.1016/j.bmcl.2018.06.049 ↗
22. 10.1021/acsami.0c1382210.1021/acsami.0c13822 ↗
23. 10.1016/j.cej.2024.15159310.1016/j.cej.2024.151593 ↗
24. 10.1016/j.apmt.2024.10227410.1016/j.apmt.2024.102274 ↗
25. 10.1016/j.cej.2023.14777010.1016/j.cej.2023.147770 ↗
26. 10.1039/D3RA07278A10.1039/D3RA07278A ↗
27. 10.1016/j.jpha.2015.11.00510.1016/j.jpha.2015.11.005 ↗
28. Han R. · Suzhou Univ. J. Med. Sci. · 2010 · 30 · 773
29. 10.1016/j.jhazmat.2021.12760210.1016/j.jhazmat.2021.127602 ↗
30. 10.1038/sj.jid.570034010.1038/sj.jid.5700340 ↗
31. 10.1016/j.cej.2021.13395610.1016/j.cej.2021.133956 ↗
32. 10.1016/j.mtbio.2025.10188710.1016/j.mtbio.2025.101887 ↗
33. 10.1016/j.ajps.2022.10.00510.1016/j.ajps.2022.10.005 ↗
34. 10.1016/j.jconrel.2023.08.05910.1016/j.jconrel.2023.08.059 ↗
35. 10.51847/Une9jqjUCl10.51847/Une9jqjUCl ↗
36. Tripathi A. · JSM Chem. · 2017 · 5 · 1042
37. 10.1186/s43094-025-00862-y10.1186/s43094-025-00862-y ↗
38. 10.1146/annurev-biochem-030222-12000010.1146/annurev-biochem-030222-120000 ↗
39. 10.7759/cureus.5289010.7759/cureus.52890 ↗
40. 10.1111/j.1399-0039.1998.tb03083.x10.1111/j.1399-0039.1998.tb03083.x ↗
41. 10.1016/j.cej.2024.15896110.1016/j.cej.2024.158961 ↗
42. 10.1186/s40168-018-0533-110.1186/s40168-018-0533-1 ↗
43. 10.1016/j.mtbio.2025.10259310.1016/j.mtbio.2025.102593 ↗
44. 10.1007/s12026-020-09149-110.1007/s12026-020-09149-1 ↗
45. 10.1016/j.mtbio.2025.10187510.1016/j.mtbio.2025.101875 ↗
46. 10.1172/JCI9742610.1172/JCI97426 ↗