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Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy
Antibiotic resistance is a big threat to public health. How to improve the therapeutic efficacy of conventional antibiotics is an effective way to address this issue. In order to enhance the antibacterial activity of conventional antibiotic erythromycin (EM), EM is conjugated to positively charged ε...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10280332/ https://www.ncbi.nlm.nih.gov/pubmed/37346938 http://dx.doi.org/10.1039/d3ra03168c |
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author | Yu, Jie Cen, Danwei Chen, Yongcheng Zhao, Hailan Xu, Mengyue Wu, Sulan Wang, Shuo Jin, Qiao Shen, Ting |
author_facet | Yu, Jie Cen, Danwei Chen, Yongcheng Zhao, Hailan Xu, Mengyue Wu, Sulan Wang, Shuo Jin, Qiao Shen, Ting |
author_sort | Yu, Jie |
collection | PubMed |
description | Antibiotic resistance is a big threat to public health. How to improve the therapeutic efficacy of conventional antibiotics is an effective way to address this issue. In order to enhance the antibacterial activity of conventional antibiotic erythromycin (EM), EM is conjugated to positively charged ε-poly-l-lysine (EPL) to obtain EPL modified EM (EPL-EM). The grafting ratio of EM can be calculated from the (1)H NMR spectrum. EPL-EM is stable in physiological environment, while EM can be readily released from EPL-EM upon incubating with esterase which can be secreted by most bacteria. Because of the presence of cationic EPL, EPL-EM showed much stronger antibacterial activity than free EM, with much lower minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). Moreover, compared to free EM, the development of drug resistance can be slowed down if EPL-EM is used, which can be ascribed to the reduction of EM dosage. Meanwhile, EPL-EM cannot induce hemolysis and cytotoxicity, which indicates that EPL-EM exhibits excellent biocompatibility. The design of EPL-EM with enhanced antibacterial activity and excellent biocompatibility provides an innovative way to combat antibiotic resistance. |
format | Online Article Text |
id | pubmed-10280332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-102803322023-06-21 Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy Yu, Jie Cen, Danwei Chen, Yongcheng Zhao, Hailan Xu, Mengyue Wu, Sulan Wang, Shuo Jin, Qiao Shen, Ting RSC Adv Chemistry Antibiotic resistance is a big threat to public health. How to improve the therapeutic efficacy of conventional antibiotics is an effective way to address this issue. In order to enhance the antibacterial activity of conventional antibiotic erythromycin (EM), EM is conjugated to positively charged ε-poly-l-lysine (EPL) to obtain EPL modified EM (EPL-EM). The grafting ratio of EM can be calculated from the (1)H NMR spectrum. EPL-EM is stable in physiological environment, while EM can be readily released from EPL-EM upon incubating with esterase which can be secreted by most bacteria. Because of the presence of cationic EPL, EPL-EM showed much stronger antibacterial activity than free EM, with much lower minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). Moreover, compared to free EM, the development of drug resistance can be slowed down if EPL-EM is used, which can be ascribed to the reduction of EM dosage. Meanwhile, EPL-EM cannot induce hemolysis and cytotoxicity, which indicates that EPL-EM exhibits excellent biocompatibility. The design of EPL-EM with enhanced antibacterial activity and excellent biocompatibility provides an innovative way to combat antibiotic resistance. The Royal Society of Chemistry 2023-06-20 /pmc/articles/PMC10280332/ /pubmed/37346938 http://dx.doi.org/10.1039/d3ra03168c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yu, Jie Cen, Danwei Chen, Yongcheng Zhao, Hailan Xu, Mengyue Wu, Sulan Wang, Shuo Jin, Qiao Shen, Ting Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
title | Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
title_full | Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
title_fullStr | Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
title_full_unstemmed | Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
title_short | Epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
title_sort | epsilon-poly-l-lysine conjugated erythromycin for enhanced antibiotic therapy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10280332/ https://www.ncbi.nlm.nih.gov/pubmed/37346938 http://dx.doi.org/10.1039/d3ra03168c |
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