Carboxymethylcellulose-based aggregation-induced emission antibacterial material for multifunctional applications
International Journal of Biological Macromolecules, ISSN: 0141-8130, Vol: 283, Issue: Pt 2, Page: 137740
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
Polysaccharides are ubiquitous in nature, typically harmless, and highly compatible with various tissues in biomedical contexts. These properties make them attractive for use in multifunctional materials. In this study, the aggregation-induced emission (AIE) antibacterial material (PLOCMC) was successfully synthesized by carboxymethylcellulose (CMC) and ε-Poly-Lysine (ε-PL). PLOCMC exhibits not only the AIE property but also a room temperature phosphorescent (RTP) phenomenon. This dual emission behavior enhances its potential applications in chemical sensing and anti-counterfeiting. Notably, PLOCMC shows low cytotoxicity and exhibits antibacterial activity against typical Gram-positive and Gram-negative bacteria, making it a potent agent against a variety of bacterial strains. Additionally, PLOCMC demonstrates specific responsiveness to Fe 3+ ions and nitrite, indicating its potential utility in food safety and monitoring applications.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0141813024085507; http://dx.doi.org/10.1016/j.ijbiomac.2024.137740; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85209075082&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/39551305; https://linkinghub.elsevier.com/retrieve/pii/S0141813024085507
Elsevier BV
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