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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.
Afiliación
  • Khan SH; Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002, India.
  • Younus H; Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002, India.
  • Allemailem KS; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraidah 51452, Saudi Arabia.
  • Almatroudi A; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraidah 51452, Saudi Arabia.
  • Alrumaihi F; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraidah 51452, Saudi Arabia.
  • Alruwetei AM; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraidah 51452, Saudi Arabia.
  • Alsahli MA; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraidah 51452, Saudi Arabia.
  • Khan A; Department of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, Buraidah, 51452, Saudi Arabia.
  • Khan MA; Department of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, Buraidah, 51452, Saudi Arabia.
Int J Nanomedicine ; 15: 3681-3693, 2020.
Article en En | MEDLINE | ID: mdl-32547022
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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Texto completo: 1 Bases de datos: MEDLINE Métodos Terapéuticos y Terapias MTCI: Plantas_medicinales Asunto principal: Piruvaldehído / Candidiasis / Fluconazol / Farmacorresistencia Fúngica / Quitosano / Nanopartículas Tipo de estudio: Prognostic_studies Idioma: En Revista: Int J Nanomedicine Año: 2020 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Métodos Terapéuticos y Terapias MTCI: Plantas_medicinales Asunto principal: Piruvaldehído / Candidiasis / Fluconazol / Farmacorresistencia Fúngica / Quitosano / Nanopartículas Tipo de estudio: Prognostic_studies Idioma: En Revista: Int J Nanomedicine Año: 2020 Tipo del documento: Article País de afiliación: India