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Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells

BACKGROUND: Final elimination of some intracellular bacterial agents, such as Brucella, is often a complex issue and impossible to achieve, primarily due to the presence and survival of the bacteria within phagocytic cells. By penetrating into the cell membrane, drug delivery nanosystems can reduce...

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Autores principales: Razei, Ali, Cheraghali, Abdol Majid, Saadati, Mojtaba, Fasihi Ramandi, Mahdi, Panahi, Yunes, Hajizade, Abbas, Siadat, Seyed Davar, Behrouzi, Ava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Salvia Medical Sciences Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344153/
https://www.ncbi.nlm.nih.gov/pubmed/34466489
http://dx.doi.org/10.31661/gmj.v8i0.1296
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author Razei, Ali
Cheraghali, Abdol Majid
Saadati, Mojtaba
Fasihi Ramandi, Mahdi
Panahi, Yunes
Hajizade, Abbas
Siadat, Seyed Davar
Behrouzi, Ava
author_facet Razei, Ali
Cheraghali, Abdol Majid
Saadati, Mojtaba
Fasihi Ramandi, Mahdi
Panahi, Yunes
Hajizade, Abbas
Siadat, Seyed Davar
Behrouzi, Ava
author_sort Razei, Ali
collection PubMed
description BACKGROUND: Final elimination of some intracellular bacterial agents, such as Brucella, is often a complex issue and impossible to achieve, primarily due to the presence and survival of the bacteria within phagocytic cells. By penetrating into the cell membrane, drug delivery nanosystems can reduce the number of intracellular bacteria. The aim of this study was to assess the efficacy of chitosan nanoparticles on the delivery of gentamicin into Brucella infected J774A.1 murine cells in vitro. MATERIALS AND METHODS: Chitosan nanoparticles (NPs) were synthesized using ionic gelation technique. The shape, size and charge of NPs, loading rate and release of the drug were investigated. Finally, the effects of gentamicin-loaded chitosan NPs (Gen-Cs) and free gentamicin on J774A.1 murine cells infected with these bacteria were examined. RESULTS: The mean size and charge of NPs were computed as 100 nm and +28mV, respectively. The loading capacity of NPs was 22%. About 70% of the drug was released from NPs during the first 8 hours. Antimicrobial activity of the two formulations showed that MIC (minimum inhibitory concentration) of the Gen-Cs and free drug was 3.1 and 6.25 µg, respectively. The minimum bactericidal concentration of the NPs-loaded drug and free drug was 6.25 and 12.5 µg, respectively. Cell culture analysis revealed that there was a significant reduction in the load of the intercellular bacteria in J774A.1 murine cells in both formulations. CONCLUSION: Our results showed the Gen-Cs have a proper potential for optimal treatment of intracellular bacterial agents.
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spelling pubmed-83441532021-08-30 Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells Razei, Ali Cheraghali, Abdol Majid Saadati, Mojtaba Fasihi Ramandi, Mahdi Panahi, Yunes Hajizade, Abbas Siadat, Seyed Davar Behrouzi, Ava Galen Med J Original Article BACKGROUND: Final elimination of some intracellular bacterial agents, such as Brucella, is often a complex issue and impossible to achieve, primarily due to the presence and survival of the bacteria within phagocytic cells. By penetrating into the cell membrane, drug delivery nanosystems can reduce the number of intracellular bacteria. The aim of this study was to assess the efficacy of chitosan nanoparticles on the delivery of gentamicin into Brucella infected J774A.1 murine cells in vitro. MATERIALS AND METHODS: Chitosan nanoparticles (NPs) were synthesized using ionic gelation technique. The shape, size and charge of NPs, loading rate and release of the drug were investigated. Finally, the effects of gentamicin-loaded chitosan NPs (Gen-Cs) and free gentamicin on J774A.1 murine cells infected with these bacteria were examined. RESULTS: The mean size and charge of NPs were computed as 100 nm and +28mV, respectively. The loading capacity of NPs was 22%. About 70% of the drug was released from NPs during the first 8 hours. Antimicrobial activity of the two formulations showed that MIC (minimum inhibitory concentration) of the Gen-Cs and free drug was 3.1 and 6.25 µg, respectively. The minimum bactericidal concentration of the NPs-loaded drug and free drug was 6.25 and 12.5 µg, respectively. Cell culture analysis revealed that there was a significant reduction in the load of the intercellular bacteria in J774A.1 murine cells in both formulations. CONCLUSION: Our results showed the Gen-Cs have a proper potential for optimal treatment of intracellular bacterial agents. Salvia Medical Sciences Ltd 2019-10-29 /pmc/articles/PMC8344153/ /pubmed/34466489 http://dx.doi.org/10.31661/gmj.v8i0.1296 Text en Copyright© 2019, Galen Medical Journal. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) )
spellingShingle Original Article
Razei, Ali
Cheraghali, Abdol Majid
Saadati, Mojtaba
Fasihi Ramandi, Mahdi
Panahi, Yunes
Hajizade, Abbas
Siadat, Seyed Davar
Behrouzi, Ava
Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells
title Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells
title_full Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells
title_fullStr Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells
title_full_unstemmed Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells
title_short Gentamicin-Loaded Chitosan Nanoparticles Improve Its Therapeutic Effects on Brucella-Infected J774A.1 Murine Cells
title_sort gentamicin-loaded chitosan nanoparticles improve its therapeutic effects on brucella-infected j774a.1 murine cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344153/
https://www.ncbi.nlm.nih.gov/pubmed/34466489
http://dx.doi.org/10.31661/gmj.v8i0.1296
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