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Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm
Fungicide is used to control fungal disease by destroying and inhibiting the fungus or fungal spores that cause the disease. However, failure to deliver fungicide to the disease region leads to ineffectiveness in the disease control. Hence, in the present study, nanotechnology has enabled the fungic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651605/ https://www.ncbi.nlm.nih.gov/pubmed/31288497 http://dx.doi.org/10.3390/molecules24132498 |
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author | Maluin, Farhatun Najat Hussein, Mohd Zobir Yusof, Nor Azah Fakurazi, Sharida Idris, Abu Seman Zainol Hilmi, Nur Hailini Jeffery Daim, Leona Daniela |
author_facet | Maluin, Farhatun Najat Hussein, Mohd Zobir Yusof, Nor Azah Fakurazi, Sharida Idris, Abu Seman Zainol Hilmi, Nur Hailini Jeffery Daim, Leona Daniela |
author_sort | Maluin, Farhatun Najat |
collection | PubMed |
description | Fungicide is used to control fungal disease by destroying and inhibiting the fungus or fungal spores that cause the disease. However, failure to deliver fungicide to the disease region leads to ineffectiveness in the disease control. Hence, in the present study, nanotechnology has enabled the fungicide active agents (hexaconazole) to be encapsulated into chitosan nanoparticles with the aim of developing a fungicide nanodelivery system that can transport them more effectively to the target cells (Ganoderma fungus). A pathogenic fungus, Ganoderma boninense (G. boninense), is destructive to oil palm whereby it can cause significant loss to oil palm plantations located in the Southeast Asian countries, especially Malaysia and Indonesia. In regard to this matter, a series of chitosan nanoparticles loaded with the fungicide, hexaconazole, was prepared using various concentrations of crosslinking agent sodium tripolyphosphate (TPP). The resulting particle size revealed that the increase of the TPP concentration produced smaller particles. In addition, the in vitro fungicide released at pH 5.5 demonstrated that the fungicide from the nanoparticles was released in a sustainable manner with a prolonged release time up to 86 h. On another note, the in vitro antifungal studies established that smaller particle size leads to lower half maximum effective concentration (EC(50)) value, which indicates higher antifungal activity against G. boninense. |
format | Online Article Text |
id | pubmed-6651605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66516052019-08-08 Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm Maluin, Farhatun Najat Hussein, Mohd Zobir Yusof, Nor Azah Fakurazi, Sharida Idris, Abu Seman Zainol Hilmi, Nur Hailini Jeffery Daim, Leona Daniela Molecules Article Fungicide is used to control fungal disease by destroying and inhibiting the fungus or fungal spores that cause the disease. However, failure to deliver fungicide to the disease region leads to ineffectiveness in the disease control. Hence, in the present study, nanotechnology has enabled the fungicide active agents (hexaconazole) to be encapsulated into chitosan nanoparticles with the aim of developing a fungicide nanodelivery system that can transport them more effectively to the target cells (Ganoderma fungus). A pathogenic fungus, Ganoderma boninense (G. boninense), is destructive to oil palm whereby it can cause significant loss to oil palm plantations located in the Southeast Asian countries, especially Malaysia and Indonesia. In regard to this matter, a series of chitosan nanoparticles loaded with the fungicide, hexaconazole, was prepared using various concentrations of crosslinking agent sodium tripolyphosphate (TPP). The resulting particle size revealed that the increase of the TPP concentration produced smaller particles. In addition, the in vitro fungicide released at pH 5.5 demonstrated that the fungicide from the nanoparticles was released in a sustainable manner with a prolonged release time up to 86 h. On another note, the in vitro antifungal studies established that smaller particle size leads to lower half maximum effective concentration (EC(50)) value, which indicates higher antifungal activity against G. boninense. MDPI 2019-07-08 /pmc/articles/PMC6651605/ /pubmed/31288497 http://dx.doi.org/10.3390/molecules24132498 Text en © 2019 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 Maluin, Farhatun Najat Hussein, Mohd Zobir Yusof, Nor Azah Fakurazi, Sharida Idris, Abu Seman Zainol Hilmi, Nur Hailini Jeffery Daim, Leona Daniela Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm |
title | Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm |
title_full | Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm |
title_fullStr | Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm |
title_full_unstemmed | Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm |
title_short | Preparation of Chitosan–Hexaconazole Nanoparticles as Fungicide Nanodelivery System for Combating Ganoderma Disease in Oil Palm |
title_sort | preparation of chitosan–hexaconazole nanoparticles as fungicide nanodelivery system for combating ganoderma disease in oil palm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651605/ https://www.ncbi.nlm.nih.gov/pubmed/31288497 http://dx.doi.org/10.3390/molecules24132498 |
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