The DOI matches its Crossref record; 232 of the 232 references it cites were found in a registry or an index.
Cationic Antimicrobial Polymers and Their Assemblies
Open accessAbstract
Cationic compounds are promising candidates for development of antimicrobial agents. Positive charges attached to surfaces, particles, polymers, peptides or bilayers have been used as antimicrobial agents by themselves or in sophisticated formulations. The main positively charged moieties in these natural or synthetic structures are quaternary ammonium groups, resulting in quaternary ammonium compounds (QACs). The advantage of amphiphilic cationic polymers when compared to small amphiphilic molecules is their enhanced microbicidal activity. Besides, many of these polymeric structures also show low toxicity to human cells; a major requirement for biomedical applications. Determination of the specific elements in polymers, which affect their antimicrobial activity, has been previously difficult due to broad molecular weight distributions and random sequences characteristic of radical polymerization. With the advances in polymerization control, selection of well defined polymers and structures are allowing greater insight into their structure-antimicrobial activity relationship. On the other hand, antimicrobial polymers grafted or self-assembled to inert or non inert vehicles can yield hybrid antimicrobial nanostructures or films, which can act as antimicrobials by themselves or deliver bioactive molecules for a variety of applications, such as wound dressing, photodynamic antimicrobial therapy, food packing and preservation and antifouling applications.
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Cited by
Jiao, Y., Niu, L.-N., Ma, S., Li, J., Tay, F. R., & Chen, J.-H. (2017) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2017.03.001 · Cited by 639
Wen, J., Weinhart, M., Lai, B., Kizhakkedathu, J., & Brooks, D. E. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.01.067 · Cited by 158
Recycled PET Nanofibers for Water Filtration Applications
Zander, N., Gillan, M., & Sweetser, D. (2016) · Materials · doi:10.3390/ma9040247 · Cited by 126
Popkin, D. L., Zilka, S., Dimaano, M., Fujioka, H., Rackley, C., Salata, R., Griffith, A., Mukherjee, P. K., Ghannoum, M. A., & Esper, F. (2017) · Pathogens and Immunity · doi:10.20411/pai.v2i2.200 · Cited by 123
Pupo, Y., Farago, P., Nadal, J., Simão, L., Esmerino, L., Gomes, O., & Gomes, J. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15058998 · Cited by 36
Metadata
- Authors
- Carmona-Ribeiro, A., & De Melo Carrasco, L.
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2013-05-10
- Volume
- 14
- Issue
- 5
- Pages
- 9906-9946
- ISSN
- 1422-0067 (ISSN-L)
- OpenAlex
- W2020045592
- Cited by
- 532
- References
- 232
- FWCI
- 17.47
- Type
- journal article
- Language
- en
- Open access
- gold
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.