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Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147
ABSTRACT: Lacticin 3147 is a dual-acting two-peptide bacteriocin which is generally active against Gram-positive bacteria, including Listeria monocytogenes and antimicrobial-resistant bacteria such as Closteroides difficile in the colon. L. monocytogenes infections can cause life-long effects in the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236048/ https://www.ncbi.nlm.nih.gov/pubmed/33876405 http://dx.doi.org/10.1007/s13346-021-00984-9 |
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author | Ryan, Aoibhín Patel, Pratikkumar O’Connor, Paula M. Ross, R. Paul Hill, Colin Hudson, Sarah P. |
author_facet | Ryan, Aoibhín Patel, Pratikkumar O’Connor, Paula M. Ross, R. Paul Hill, Colin Hudson, Sarah P. |
author_sort | Ryan, Aoibhín |
collection | PubMed |
description | ABSTRACT: Lacticin 3147 is a dual-acting two-peptide bacteriocin which is generally active against Gram-positive bacteria, including Listeria monocytogenes and antimicrobial-resistant bacteria such as Closteroides difficile in the colon. L. monocytogenes infections can cause life-long effects in the elderly and vulnerable and can cause severe complications in pregnant women. C. difficile causes one of the most common healthcare-associated infections and can be fatal in vulnerable groups such as the elderly. Although lacticin 3147 is degraded by intestinal proteases and has poor aqueous solubility, encapsulation of the bacteriocin could enable its use as an antimicrobial for treating these bacterial infections locally in the gastrointestinal tract. Lacticin 3147 displayed activity in aqueous solutions at a range of pH values and in gastric and intestinal fluids. Exposure to trypsin and α-chymotrypsin resulted in complete inactivation, implying that lacticin 3147 should be protected from these enzymes to achieve successful local delivery to the gastrointestinal tract. The amount of lacticin 3147 dissolved, i.e. its solution concentration, in water or buffered solutions at pH 1.6 and 7.4 was low and varied with time but increased and was stabilized in gastrointestinal fluids by the phospholipid and bile salt components present. Thus, the feasibility of a solid lipid nanoparticle (SLN) delivery system for local administration of lacticin 3147 was investigated. Bacteriocin activity was observed after encapsulation and release from a lipid matrix. Moreover, activity was seen after exposure to degrading enzymes. Further optimization of SLN delivery systems could enable the successful pharmaceutical development of active lacticin 3147 as an alternative to traditional antibiotics. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-8236048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-82360482021-07-09 Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 Ryan, Aoibhín Patel, Pratikkumar O’Connor, Paula M. Ross, R. Paul Hill, Colin Hudson, Sarah P. Drug Deliv Transl Res Original Article ABSTRACT: Lacticin 3147 is a dual-acting two-peptide bacteriocin which is generally active against Gram-positive bacteria, including Listeria monocytogenes and antimicrobial-resistant bacteria such as Closteroides difficile in the colon. L. monocytogenes infections can cause life-long effects in the elderly and vulnerable and can cause severe complications in pregnant women. C. difficile causes one of the most common healthcare-associated infections and can be fatal in vulnerable groups such as the elderly. Although lacticin 3147 is degraded by intestinal proteases and has poor aqueous solubility, encapsulation of the bacteriocin could enable its use as an antimicrobial for treating these bacterial infections locally in the gastrointestinal tract. Lacticin 3147 displayed activity in aqueous solutions at a range of pH values and in gastric and intestinal fluids. Exposure to trypsin and α-chymotrypsin resulted in complete inactivation, implying that lacticin 3147 should be protected from these enzymes to achieve successful local delivery to the gastrointestinal tract. The amount of lacticin 3147 dissolved, i.e. its solution concentration, in water or buffered solutions at pH 1.6 and 7.4 was low and varied with time but increased and was stabilized in gastrointestinal fluids by the phospholipid and bile salt components present. Thus, the feasibility of a solid lipid nanoparticle (SLN) delivery system for local administration of lacticin 3147 was investigated. Bacteriocin activity was observed after encapsulation and release from a lipid matrix. Moreover, activity was seen after exposure to degrading enzymes. Further optimization of SLN delivery systems could enable the successful pharmaceutical development of active lacticin 3147 as an alternative to traditional antibiotics. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2021-04-19 2021 /pmc/articles/PMC8236048/ /pubmed/33876405 http://dx.doi.org/10.1007/s13346-021-00984-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Ryan, Aoibhín Patel, Pratikkumar O’Connor, Paula M. Ross, R. Paul Hill, Colin Hudson, Sarah P. Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
title | Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
title_full | Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
title_fullStr | Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
title_full_unstemmed | Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
title_short | Pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
title_sort | pharmaceutical design of a delivery system for the bacteriocin lacticin 3147 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236048/ https://www.ncbi.nlm.nih.gov/pubmed/33876405 http://dx.doi.org/10.1007/s13346-021-00984-9 |
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