journal article·2022-02-07

Fluorescent Cellulose Wipe as a New and Sustainable Light-Activated Antibacterial and Antiviral Agent

Zhen Zhang, David G Whitten, Alison Kell

ACS Materials Letters· Volume 4· Issue 2
Publisher page

Abstract

The ongoing global COVID-19 pandemic has created awareness toward the development of antibacterial and antiviral materials. In this communication, we report a new and promising antibacterial and antiviral material based on cationic conjugated oligomer electrolytes with imidazole groups (c-OPE-Im) and 1,4-diazabicyclo [2,2,2]-octane pendant groups (c-OPE-DABCO) and a cellulose wipe via a simple dip-coating process. Specific interactions between c-OPE and the cellulose wipe such as the ion-dipole and electrostatic interactions drive the successful coating process, resulting in highly fluorescent materials. The c-OPE-Im coated wipe possesses impressive killing efficiency against Escherichia coli (E. coli) under 5–10 min light-activation. The generation of reactive oxygen species from both “free” c-OPE delivered from the coated wipe and undelivered OPE is proposed to be the antibacterial mechanism. The c-OPE coated wipe also exhibited an appreciable inactivation of SARS-CoV-2, where a total inactivation was achieved in 20–30 min light-activation. The simple preparation, sustainable nature of the cellulose wipe, and promising antibacterial and antiviral performance make the current surface-coated wipes attractive as a new antibacterial and antiviral agent.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Photodynamic Therapy Research Studies · Nanoplatforms for cancer theranostics · Polydiacetylene-based materials and applications

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

Affiliations

Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, New Mexico 87131, United States

Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, New Mexico 87131, United States

Department of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, Albuquerque, New Mexico 87131, United States

Funding

Biosafe Technologies LLC · US National Institutes of Health

References (27)

Show source-provided references
1. 10.1002/adfm.20180214010.1002/adfm.201802140 ↗
2. 10.1002/adma.20190410610.1002/adma.201904106 ↗
3. 10.1016/j.bcab.2016.05.00210.1016/j.bcab.2016.05.002 ↗
4. 10.1016/j.btre.2020.e0042710.1016/j.btre.2020.e00427 ↗
5. 10.1021/acsabm.1c0007710.1021/acsabm.1c00077 ↗
6. 10.1039/b311900a10.1039/b311900a ↗
7. 10.1039/C8PP00534F10.1039/C8PP00534F ↗
8. 10.5978/islsm.27_18-RA-0110.5978/islsm.27_18-RA-01 ↗
9. 10.1039/b502125a10.1039/b502125a ↗
10. 10.1002/adhm.20190013210.1002/adhm.201900132 ↗
11. 10.1021/acs.langmuir.8b0181010.1021/acs.langmuir.8b01810 ↗
12. 10.1021/ar50004a00210.1021/ar50004a002 ↗
13. 10.1021/j100172a03810.1021/j100172a038 ↗
14. 10.1073/pnas.061132810410.1073/pnas.0611328104 ↗
15. 10.1021/am200644g10.1021/am200644g ↗
16. 10.1021/jz101088k10.1021/jz101088k ↗
17. 10.1016/j.colsurfb.2014.01.03310.1016/j.colsurfb.2014.01.033 ↗
18. 10.1016/j.colsurfb.2014.12.04310.1016/j.colsurfb.2014.12.043 ↗
19. 10.1021/acs.chemmater.7b0179610.1021/acs.chemmater.7b01796 ↗
20. 10.1111/php.1301310.1111/php.13013 ↗
21. 10.1021/acsami.6b1624310.1021/acsami.6b16243 ↗
22. 10.1016/0166-6622(89)80243-410.1016/0166-6622(89)80243-4 ↗
23. 10.1016/j.jviromet.2014.10.00810.1016/j.jviromet.2014.10.008 ↗
24. 10.1021/jp983921t10.1021/jp983921t ↗
25. 10.1038/nmat75010.1038/nmat750 ↗
26. 10.1016/j.addr.2012.02.00310.1016/j.addr.2012.02.003 ↗
27. 10.1021/la401983h10.1021/la401983h ↗