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An effective nano drug delivery and combination therapy for the treatment of Tuberculosis

Drug resistance in tuberculosis is exacerbating the threat this disease is posing to human beings. Antibiotics that were once effective against the causative agent, Mycobacterium tuberculosis (Mtb), are now no longer usable against multi- and extensively drug-resistant strains of this pathogen. To a...

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Autores principales: Sheikhpour, Mojgan, Delorme, Vincent, Kasaeian, Alibakhsh, Amiri, Vahid, Masoumi, Morteza, Sadeghinia, Mohammad, Ebrahimzadeh, Nayereh, Maleki, Mobina, Pourazar, Shahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185718/
https://www.ncbi.nlm.nih.gov/pubmed/35688860
http://dx.doi.org/10.1038/s41598-022-13682-4
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author Sheikhpour, Mojgan
Delorme, Vincent
Kasaeian, Alibakhsh
Amiri, Vahid
Masoumi, Morteza
Sadeghinia, Mohammad
Ebrahimzadeh, Nayereh
Maleki, Mobina
Pourazar, Shahin
author_facet Sheikhpour, Mojgan
Delorme, Vincent
Kasaeian, Alibakhsh
Amiri, Vahid
Masoumi, Morteza
Sadeghinia, Mohammad
Ebrahimzadeh, Nayereh
Maleki, Mobina
Pourazar, Shahin
author_sort Sheikhpour, Mojgan
collection PubMed
description Drug resistance in tuberculosis is exacerbating the threat this disease is posing to human beings. Antibiotics that were once effective against the causative agent, Mycobacterium tuberculosis (Mtb), are now no longer usable against multi- and extensively drug-resistant strains of this pathogen. To address this issue, new drug combinations and novel methods for targeted drug delivery could be of considerable value. In addition, studies have shown that the use of the antidepressant drug fluoxetine, a serotonin reuptake inhibitor, can be useful in the treatment of infectious diseases, including bacterial infections. In this study, an isoniazid and fluoxetine-conjugated multi-walled carbon nanotube nanofluid were designed to increase drug delivery efficiency alongside eliminating drug resistance in vitro. The prepared nanofluid was tested against Mtb. Expression levels of inhA and katG mRNAs were detected by Real-time PCR. ELISA was applied to measure levels of cytokine secretion (TNF-α, and IL-6) from infected macrophages treated with the nano delivery system. The results showed that these nano-drug delivery systems are effective for fluoxetine at far lower doses than for free drugs. Fluoxetine also has an additive effect on the effect of isoniazid, and their concomitant use in the delivery system can have significant effects in treating infection of all clinical strains of Mtb. In addition, it was found that the expression of isoniazid resistance genes, including inhA, katG, and the secretion of cytokines TNFα and IL6 under the influence of this drug delivery system is well regulated. It was shown that the drug conjugation can improve the antibacterial activity of them in all strains and these two drugs have an additive effect on each other both in free and conjugated forms. This nano-drug delivery method combined with host targeted molecules could be a game-changer in the development of a new generation of antibiotics that have high therapeutic efficiencies, low side effects, and the potential to overcome the problem of drug resistance.
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spelling pubmed-91857182022-06-10 An effective nano drug delivery and combination therapy for the treatment of Tuberculosis Sheikhpour, Mojgan Delorme, Vincent Kasaeian, Alibakhsh Amiri, Vahid Masoumi, Morteza Sadeghinia, Mohammad Ebrahimzadeh, Nayereh Maleki, Mobina Pourazar, Shahin Sci Rep Article Drug resistance in tuberculosis is exacerbating the threat this disease is posing to human beings. Antibiotics that were once effective against the causative agent, Mycobacterium tuberculosis (Mtb), are now no longer usable against multi- and extensively drug-resistant strains of this pathogen. To address this issue, new drug combinations and novel methods for targeted drug delivery could be of considerable value. In addition, studies have shown that the use of the antidepressant drug fluoxetine, a serotonin reuptake inhibitor, can be useful in the treatment of infectious diseases, including bacterial infections. In this study, an isoniazid and fluoxetine-conjugated multi-walled carbon nanotube nanofluid were designed to increase drug delivery efficiency alongside eliminating drug resistance in vitro. The prepared nanofluid was tested against Mtb. Expression levels of inhA and katG mRNAs were detected by Real-time PCR. ELISA was applied to measure levels of cytokine secretion (TNF-α, and IL-6) from infected macrophages treated with the nano delivery system. The results showed that these nano-drug delivery systems are effective for fluoxetine at far lower doses than for free drugs. Fluoxetine also has an additive effect on the effect of isoniazid, and their concomitant use in the delivery system can have significant effects in treating infection of all clinical strains of Mtb. In addition, it was found that the expression of isoniazid resistance genes, including inhA, katG, and the secretion of cytokines TNFα and IL6 under the influence of this drug delivery system is well regulated. It was shown that the drug conjugation can improve the antibacterial activity of them in all strains and these two drugs have an additive effect on each other both in free and conjugated forms. This nano-drug delivery method combined with host targeted molecules could be a game-changer in the development of a new generation of antibiotics that have high therapeutic efficiencies, low side effects, and the potential to overcome the problem of drug resistance. Nature Publishing Group UK 2022-06-10 /pmc/articles/PMC9185718/ /pubmed/35688860 http://dx.doi.org/10.1038/s41598-022-13682-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sheikhpour, Mojgan
Delorme, Vincent
Kasaeian, Alibakhsh
Amiri, Vahid
Masoumi, Morteza
Sadeghinia, Mohammad
Ebrahimzadeh, Nayereh
Maleki, Mobina
Pourazar, Shahin
An effective nano drug delivery and combination therapy for the treatment of Tuberculosis
title An effective nano drug delivery and combination therapy for the treatment of Tuberculosis
title_full An effective nano drug delivery and combination therapy for the treatment of Tuberculosis
title_fullStr An effective nano drug delivery and combination therapy for the treatment of Tuberculosis
title_full_unstemmed An effective nano drug delivery and combination therapy for the treatment of Tuberculosis
title_short An effective nano drug delivery and combination therapy for the treatment of Tuberculosis
title_sort effective nano drug delivery and combination therapy for the treatment of tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185718/
https://www.ncbi.nlm.nih.gov/pubmed/35688860
http://dx.doi.org/10.1038/s41598-022-13682-4
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