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Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model

BACKGROUND: Fungal infections are becoming more prevalent and threatening because of the continuous emergence of azole-resistant fungal infections. The present study was aimed to assess the activity of free Methylglyoxal (MG) or MG-conjugated chitosan nanoparticles (MGCN) against fluconazole-resista...

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Autores principales: Khan, Shaheer Hasan, Younus, Hina, Allemailem, Khaled S, Almatroudi, Ahmad, Alrumaihi, Faris, Alruwetei, Abdulmohsen M, Alsahli, Mohammed A, Khan, Arif, Khan, Masood Alam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261666/
https://www.ncbi.nlm.nih.gov/pubmed/32547022
http://dx.doi.org/10.2147/IJN.S249625
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author Khan, Shaheer Hasan
Younus, Hina
Allemailem, Khaled S
Almatroudi, Ahmad
Alrumaihi, Faris
Alruwetei, Abdulmohsen M
Alsahli, Mohammed A
Khan, Arif
Khan, Masood Alam
author_facet Khan, Shaheer Hasan
Younus, Hina
Allemailem, Khaled S
Almatroudi, Ahmad
Alrumaihi, Faris
Alruwetei, Abdulmohsen M
Alsahli, Mohammed A
Khan, Arif
Khan, Masood Alam
author_sort Khan, Shaheer Hasan
collection PubMed
description BACKGROUND: Fungal infections are becoming more prevalent and threatening because of the continuous emergence of azole-resistant fungal infections. The present study was aimed to assess the activity of free Methylglyoxal (MG) or MG-conjugated chitosan nanoparticles (MGCN) against fluconazole-resistant Candida albicans. MATERIALS AND METHODS: A novel formulation of MGCN was prepared and characterized to determine their size, shape and polydispersity index. Moreover, the efficacy of fluconazole or MG or MGCN was determined against intracellular C. albicans in macrophages and the systematic candidiasis in a murine model. The safety of MG or MGCN was tested in mice by analyzing the levels of hepatic and renal toxicity parameters. RESULTS: Candida albicans did not respond to fluconazole, even at the highest dose of 20 mg/kg, whereas MG and MGCN effectively eliminated C. albicans from the macrophages and infected mice. Mice in the group treated with MGCN at a dose of 10 mg/kg exhibited a 90% survival rate and showed the lowest fungal load in the kidney, whereas the mice treated with free MG at the same dose exhibited 50% survival rate. Moreover, the administration of MG or MGCN did not induce any liver and kidney toxicity in the treated mice. CONCLUSION: The findings of the present work suggest that MGCN may be proved a promising therapeutic formulation to treat azole-resistant C. albicans infections.
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spelling pubmed-72616662020-06-15 Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model Khan, Shaheer Hasan Younus, Hina Allemailem, Khaled S Almatroudi, Ahmad Alrumaihi, Faris Alruwetei, Abdulmohsen M Alsahli, Mohammed A Khan, Arif Khan, Masood Alam Int J Nanomedicine Original Research BACKGROUND: Fungal infections are becoming more prevalent and threatening because of the continuous emergence of azole-resistant fungal infections. The present study was aimed to assess the activity of free Methylglyoxal (MG) or MG-conjugated chitosan nanoparticles (MGCN) against fluconazole-resistant Candida albicans. MATERIALS AND METHODS: A novel formulation of MGCN was prepared and characterized to determine their size, shape and polydispersity index. Moreover, the efficacy of fluconazole or MG or MGCN was determined against intracellular C. albicans in macrophages and the systematic candidiasis in a murine model. The safety of MG or MGCN was tested in mice by analyzing the levels of hepatic and renal toxicity parameters. RESULTS: Candida albicans did not respond to fluconazole, even at the highest dose of 20 mg/kg, whereas MG and MGCN effectively eliminated C. albicans from the macrophages and infected mice. Mice in the group treated with MGCN at a dose of 10 mg/kg exhibited a 90% survival rate and showed the lowest fungal load in the kidney, whereas the mice treated with free MG at the same dose exhibited 50% survival rate. Moreover, the administration of MG or MGCN did not induce any liver and kidney toxicity in the treated mice. CONCLUSION: The findings of the present work suggest that MGCN may be proved a promising therapeutic formulation to treat azole-resistant C. albicans infections. Dove 2020-05-26 /pmc/articles/PMC7261666/ /pubmed/32547022 http://dx.doi.org/10.2147/IJN.S249625 Text en © 2020 Khan et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Khan, Shaheer Hasan
Younus, Hina
Allemailem, Khaled S
Almatroudi, Ahmad
Alrumaihi, Faris
Alruwetei, Abdulmohsen M
Alsahli, Mohammed A
Khan, Arif
Khan, Masood Alam
Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model
title Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model
title_full Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model
title_fullStr Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model
title_full_unstemmed Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model
title_short Potential of Methylglyoxal-Conjugated Chitosan Nanoparticles in Treatment of Fluconazole-Resistant Candida albicans Infection in a Murine Model
title_sort potential of methylglyoxal-conjugated chitosan nanoparticles in treatment of fluconazole-resistant candida albicans infection in a murine model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261666/
https://www.ncbi.nlm.nih.gov/pubmed/32547022
http://dx.doi.org/10.2147/IJN.S249625
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