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Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance
An antimicrobial decapeptide, KSL-W (KKVVFWVKFK-CONH(2)), which could maintain stable antimicrobial activity in saliva, has therefore been widely used to inhibit biofilm formation on teeth and prevent the growth of oral microorganisms for related infectious diseases treatment. In order to control th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151433/ https://www.ncbi.nlm.nih.gov/pubmed/28961197 http://dx.doi.org/10.3390/molecules22101637 |
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author | Li, Yuanyuan Na, Rongwei Wang, Xiumei Liu, Huiying Zhao, Lingyun Sun, Xiaodan Ma, Guowu Cui, Fuzhai |
author_facet | Li, Yuanyuan Na, Rongwei Wang, Xiumei Liu, Huiying Zhao, Lingyun Sun, Xiaodan Ma, Guowu Cui, Fuzhai |
author_sort | Li, Yuanyuan |
collection | PubMed |
description | An antimicrobial decapeptide, KSL-W (KKVVFWVKFK-CONH(2)), which could maintain stable antimicrobial activity in saliva, has therefore been widely used to inhibit biofilm formation on teeth and prevent the growth of oral microorganisms for related infectious diseases treatment. In order to control the release of KSL-W for long-term bacterial resistance, KSL-W-loaded PLGA/chitosan composite microspheres (KSL/PLGA/CS MSs) were prepared by electrospraying and combined crosslinking-emulsion methods. Different formulations of microspheres were characterized as to surface morphology, size distribution, encapsulation efficiency, in vitro drug release, and antimicrobial activity. Antibacterial experiment demonstrated the prolonged antimicrobial and inhibitory effects of KSL/PLGA/CS MSs on oral bacteria. Moreover, the cell proliferation assay proved that the released KSL-W antibacterial dosage had no cytotoxicity to the growth of osteoblast MC3T3-E1. Thus, our study suggested that the KSL-W-loaded PLGA/CS composite microspheres may have potentially therapeutic applications as an effective drug delivery system in the treatment of oral infectious diseases such as periodontitis and periodontitis, and also within bone graft substitutes for alveolar bone augmentation. |
format | Online Article Text |
id | pubmed-6151433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61514332018-11-13 Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance Li, Yuanyuan Na, Rongwei Wang, Xiumei Liu, Huiying Zhao, Lingyun Sun, Xiaodan Ma, Guowu Cui, Fuzhai Molecules Article An antimicrobial decapeptide, KSL-W (KKVVFWVKFK-CONH(2)), which could maintain stable antimicrobial activity in saliva, has therefore been widely used to inhibit biofilm formation on teeth and prevent the growth of oral microorganisms for related infectious diseases treatment. In order to control the release of KSL-W for long-term bacterial resistance, KSL-W-loaded PLGA/chitosan composite microspheres (KSL/PLGA/CS MSs) were prepared by electrospraying and combined crosslinking-emulsion methods. Different formulations of microspheres were characterized as to surface morphology, size distribution, encapsulation efficiency, in vitro drug release, and antimicrobial activity. Antibacterial experiment demonstrated the prolonged antimicrobial and inhibitory effects of KSL/PLGA/CS MSs on oral bacteria. Moreover, the cell proliferation assay proved that the released KSL-W antibacterial dosage had no cytotoxicity to the growth of osteoblast MC3T3-E1. Thus, our study suggested that the KSL-W-loaded PLGA/CS composite microspheres may have potentially therapeutic applications as an effective drug delivery system in the treatment of oral infectious diseases such as periodontitis and periodontitis, and also within bone graft substitutes for alveolar bone augmentation. MDPI 2017-09-29 /pmc/articles/PMC6151433/ /pubmed/28961197 http://dx.doi.org/10.3390/molecules22101637 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Yuanyuan Na, Rongwei Wang, Xiumei Liu, Huiying Zhao, Lingyun Sun, Xiaodan Ma, Guowu Cui, Fuzhai Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance |
title | Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance |
title_full | Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance |
title_fullStr | Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance |
title_full_unstemmed | Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance |
title_short | Fabrication of Antimicrobial Peptide-Loaded PLGA/Chitosan Composite Microspheres for Long-Acting Bacterial Resistance |
title_sort | fabrication of antimicrobial peptide-loaded plga/chitosan composite microspheres for long-acting bacterial resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151433/ https://www.ncbi.nlm.nih.gov/pubmed/28961197 http://dx.doi.org/10.3390/molecules22101637 |
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