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2000
Volume 20, Issue 9
  • ISSN: 1389-2037
  • E-ISSN: 1875-5550

Abstract

Cationic antimicrobial peptides (CAMPs) can be considered as new potential therapeutic agents for Tuberculosis treatment with a specific amino acid sequence. New studies can be developed in the future to improve the pharmacological properties of CAMPs and also understand possible resistance mechanisms. This review discusses the principal properties of natural and/or synthetic CAMPs, and how these new peptides have a significant specificity for Mycobacterium tuberculosis. Also, we propose some alternative strategies to enhance the therapeutic activity of these CAMPs that include coadministration with nanoparticles and/or classic drugs.

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/content/journals/cpps/10.2174/1389203720666190626160057
2019-09-01
2024-11-15
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