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Nanosized Drug Delivery Systems to Fight Tuberculosis

Tuberculosis (TB) is currently the second deadliest infectious disease. Existing antitubercular therapies are long, complex, and have severe side effects that result in low patient compliance. In this context, nanosized drug delivery systems (DDSs) have the potential to optimize the treatment’s effi...

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Autores principales: Bourguignon, Tom, Godinez-Leon, Jesus Alfredo, Gref, Ruxandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964171/
https://www.ncbi.nlm.nih.gov/pubmed/36839715
http://dx.doi.org/10.3390/pharmaceutics15020393
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author Bourguignon, Tom
Godinez-Leon, Jesus Alfredo
Gref, Ruxandra
author_facet Bourguignon, Tom
Godinez-Leon, Jesus Alfredo
Gref, Ruxandra
author_sort Bourguignon, Tom
collection PubMed
description Tuberculosis (TB) is currently the second deadliest infectious disease. Existing antitubercular therapies are long, complex, and have severe side effects that result in low patient compliance. In this context, nanosized drug delivery systems (DDSs) have the potential to optimize the treatment’s efficiency while reducing its toxicity. Hundreds of publications illustrate the growing interest in this field. In this review, the main challenges related to the use of drug nanocarriers to fight TB are overviewed. Relevant publications regarding DDSs for the treatment of TB are classified according to the encapsulated drugs, from first-line to second-line drugs. The physicochemical and biological properties of the investigated formulations are listed. DDSs could simultaneously (i) optimize the therapy’s antibacterial effects; (ii) reduce the doses; (iii) reduce the posology; (iv) diminish the toxicity; and as a global result, (v) mitigate the emergence of resistant strains. Moreover, we highlight that host-directed therapy using nanoparticles (NPs) is a recent promising trend. Although the research on nanosized DDSs for TB treatment is expanding, clinical applications have yet to be developed. Most studies are only dedicated to the development of new formulations, without the in vivo proof of concept. In the near future, it is expected that NPs prepared by “green” scalable methods, with intrinsic antibacterial properties and capable of co-encapsulating synergistic drugs, may find applications to fight TB.
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spelling pubmed-99641712023-02-26 Nanosized Drug Delivery Systems to Fight Tuberculosis Bourguignon, Tom Godinez-Leon, Jesus Alfredo Gref, Ruxandra Pharmaceutics Review Tuberculosis (TB) is currently the second deadliest infectious disease. Existing antitubercular therapies are long, complex, and have severe side effects that result in low patient compliance. In this context, nanosized drug delivery systems (DDSs) have the potential to optimize the treatment’s efficiency while reducing its toxicity. Hundreds of publications illustrate the growing interest in this field. In this review, the main challenges related to the use of drug nanocarriers to fight TB are overviewed. Relevant publications regarding DDSs for the treatment of TB are classified according to the encapsulated drugs, from first-line to second-line drugs. The physicochemical and biological properties of the investigated formulations are listed. DDSs could simultaneously (i) optimize the therapy’s antibacterial effects; (ii) reduce the doses; (iii) reduce the posology; (iv) diminish the toxicity; and as a global result, (v) mitigate the emergence of resistant strains. Moreover, we highlight that host-directed therapy using nanoparticles (NPs) is a recent promising trend. Although the research on nanosized DDSs for TB treatment is expanding, clinical applications have yet to be developed. Most studies are only dedicated to the development of new formulations, without the in vivo proof of concept. In the near future, it is expected that NPs prepared by “green” scalable methods, with intrinsic antibacterial properties and capable of co-encapsulating synergistic drugs, may find applications to fight TB. MDPI 2023-01-24 /pmc/articles/PMC9964171/ /pubmed/36839715 http://dx.doi.org/10.3390/pharmaceutics15020393 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bourguignon, Tom
Godinez-Leon, Jesus Alfredo
Gref, Ruxandra
Nanosized Drug Delivery Systems to Fight Tuberculosis
title Nanosized Drug Delivery Systems to Fight Tuberculosis
title_full Nanosized Drug Delivery Systems to Fight Tuberculosis
title_fullStr Nanosized Drug Delivery Systems to Fight Tuberculosis
title_full_unstemmed Nanosized Drug Delivery Systems to Fight Tuberculosis
title_short Nanosized Drug Delivery Systems to Fight Tuberculosis
title_sort nanosized drug delivery systems to fight tuberculosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964171/
https://www.ncbi.nlm.nih.gov/pubmed/36839715
http://dx.doi.org/10.3390/pharmaceutics15020393
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