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...

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Main Authors: Maluin, Farhatun Najat, Hussein, Mohd Zobir, Yusof, Nor Azah, Fakurazi, Sharida, Abu Seman, Idris, Zainol Hilmi, Nur Hailini, Jeffery Daim, Leona Daniela
Format: Article
Language:English
Published: MDPI 2019
Online Access:http://psasir.upm.edu.my/id/eprint/38332/
http://psasir.upm.edu.my/id/eprint/38332/1/38332.pdf
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author Maluin, Farhatun Najat
Hussein, Mohd Zobir
Yusof, Nor Azah
Fakurazi, Sharida
Abu Seman, Idris
Zainol Hilmi, Nur Hailini
Jeffery Daim, Leona Daniela
author_facet Maluin, Farhatun Najat
Hussein, Mohd Zobir
Yusof, Nor Azah
Fakurazi, Sharida
Abu Seman, Idris
Zainol Hilmi, Nur Hailini
Jeffery Daim, Leona Daniela
author_sort Maluin, Farhatun Najat
building UPM Institutional Repository
collection Online Access
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 (EC50) value, which indicates higher antifungal activity against G. boninense.
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spelling upm-383322020-05-04T16:18:27Z http://psasir.upm.edu.my/id/eprint/38332/ 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 Abu Seman, Idris Zainol Hilmi, Nur Hailini Jeffery Daim, Leona Daniela 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 (EC50) value, which indicates higher antifungal activity against G. boninense. MDPI 2019 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/38332/1/38332.pdf Maluin, Farhatun Najat and Hussein, Mohd Zobir and Yusof, Nor Azah and Fakurazi, Sharida and Abu Seman, Idris and Zainol Hilmi, Nur Hailini and Jeffery Daim, Leona Daniela (2019) Preparation of chitosan–hexaconazole nanoparticles as fungicide nanodelivery system for combating Ganoderma disease in oil palm. Molecules, 24 (13). art. no. 2498. pp. 1-16. ISSN 1420-3049 https://www.mdpi.com/1420-3049/24/13/2498 10.3390/molecules24132498
spellingShingle Maluin, Farhatun Najat
Hussein, Mohd Zobir
Yusof, Nor Azah
Fakurazi, Sharida
Abu Seman, Idris
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
url http://psasir.upm.edu.my/id/eprint/38332/
http://psasir.upm.edu.my/id/eprint/38332/
http://psasir.upm.edu.my/id/eprint/38332/
http://psasir.upm.edu.my/id/eprint/38332/1/38332.pdf