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A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed
The controlled supply of bioactive molecules is a subject of debate in animal nutrition. The release of bioactive molecules in the target organ, in this case the intestine, results in improved feed, as well as having a lower environmental impact. However, the degradation of bioactive molecules’ in t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674955/ https://www.ncbi.nlm.nih.gov/pubmed/37999319 http://dx.doi.org/10.3390/nano13222965 |
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author | Guagliano, Marianna Cristiani, Cinzia Dell’Anno, Matteo Dotelli, Giovanni Finocchio, Elisabetta Lacalamita, Maria Mesto, Ernesto Reggi, Serena Rossi, Luciana Schingaro, Emanuela |
author_facet | Guagliano, Marianna Cristiani, Cinzia Dell’Anno, Matteo Dotelli, Giovanni Finocchio, Elisabetta Lacalamita, Maria Mesto, Ernesto Reggi, Serena Rossi, Luciana Schingaro, Emanuela |
author_sort | Guagliano, Marianna |
collection | PubMed |
description | The controlled supply of bioactive molecules is a subject of debate in animal nutrition. The release of bioactive molecules in the target organ, in this case the intestine, results in improved feed, as well as having a lower environmental impact. However, the degradation of bioactive molecules’ in transit in the gastrointestinal passage is still an unresolved issue. This paper discusses the feasibility of a simple and cost-effective procedure to bypass the degradation problem. A solid/liquid adsorption procedure was applied, and the operating parameters (pH, reaction time, and LY initial concentration) were studied. Lysozyme is used in this work as a representative bioactive molecule, while Adsorbo(®), a commercial mixture of clay minerals and zeolites which meets current feed regulations, is used as the carrier. A maximum LY loading of 32 mg(LY)/g(AD) (LY(32)-AD) was obtained, with fixing pH in the range 7.5–8, initial LY content at 37.5 mg(LY)/g(AD), and reaction time at 30 min. A full characterisation of the hybrid organoclay highlighted that LY molecules were homogeneously spread on the carrier’s surface, where the LY–carrier interaction was mainly due to charge interaction. Preliminary release tests performed on the LY(32)-AD synthesised sample showed a higher releasing capacity, raising the pH from 3 to 7. In addition, a preliminary Trolox equivalent antioxidant capacity (TEAC) assay showed an antioxidant capacity for the LY of 1.47 ± 0.18 µmol TroloxEq/g with an inhibition percentage of 33.20 ± 3.94%. |
format | Online Article Text |
id | pubmed-10674955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106749552023-11-17 A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed Guagliano, Marianna Cristiani, Cinzia Dell’Anno, Matteo Dotelli, Giovanni Finocchio, Elisabetta Lacalamita, Maria Mesto, Ernesto Reggi, Serena Rossi, Luciana Schingaro, Emanuela Nanomaterials (Basel) Article The controlled supply of bioactive molecules is a subject of debate in animal nutrition. The release of bioactive molecules in the target organ, in this case the intestine, results in improved feed, as well as having a lower environmental impact. However, the degradation of bioactive molecules’ in transit in the gastrointestinal passage is still an unresolved issue. This paper discusses the feasibility of a simple and cost-effective procedure to bypass the degradation problem. A solid/liquid adsorption procedure was applied, and the operating parameters (pH, reaction time, and LY initial concentration) were studied. Lysozyme is used in this work as a representative bioactive molecule, while Adsorbo(®), a commercial mixture of clay minerals and zeolites which meets current feed regulations, is used as the carrier. A maximum LY loading of 32 mg(LY)/g(AD) (LY(32)-AD) was obtained, with fixing pH in the range 7.5–8, initial LY content at 37.5 mg(LY)/g(AD), and reaction time at 30 min. A full characterisation of the hybrid organoclay highlighted that LY molecules were homogeneously spread on the carrier’s surface, where the LY–carrier interaction was mainly due to charge interaction. Preliminary release tests performed on the LY(32)-AD synthesised sample showed a higher releasing capacity, raising the pH from 3 to 7. In addition, a preliminary Trolox equivalent antioxidant capacity (TEAC) assay showed an antioxidant capacity for the LY of 1.47 ± 0.18 µmol TroloxEq/g with an inhibition percentage of 33.20 ± 3.94%. MDPI 2023-11-17 /pmc/articles/PMC10674955/ /pubmed/37999319 http://dx.doi.org/10.3390/nano13222965 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Guagliano, Marianna Cristiani, Cinzia Dell’Anno, Matteo Dotelli, Giovanni Finocchio, Elisabetta Lacalamita, Maria Mesto, Ernesto Reggi, Serena Rossi, Luciana Schingaro, Emanuela A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed |
title | A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed |
title_full | A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed |
title_fullStr | A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed |
title_full_unstemmed | A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed |
title_short | A Commercial Clay-Based Material as a Carrier for Targeted Lysozyme Delivery in Animal Feed |
title_sort | commercial clay-based material as a carrier for targeted lysozyme delivery in animal feed |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674955/ https://www.ncbi.nlm.nih.gov/pubmed/37999319 http://dx.doi.org/10.3390/nano13222965 |
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