AI Article Synopsis

  • - The emergence of antibiotic resistance in pathogenic microorganisms poses a significant global health threat, prompting the need for new antibiotic solutions.
  • - Researchers are exploring scorpion venom from Northeastern Brazil, which contains bioactive molecules that could be developed into effective antimicrobial agents, despite challenges related to the venom’s cytotoxicity.
  • - The study produced chitosan nanoparticles loaded with scorpion venom, showing promising results: they had appropriate sizes and stability, and the nanoparticles significantly enhanced the venom's antimicrobial effects against various bacteria and yeast, indicating their potential as new therapeutic agents.

Article Abstract

The rapid resistance developed by pathogenic microorganisms against the current antimicrobial pool represents a serious global public health problem, leading to the search for new antibiotic agents. The scorpion , an abundant species in Northeastern Brazil, presents a rich arsenal of bioactive molecules in its venom, with high potential for biotechnological applications. However, venom cytotoxicity constitutes a barrier to the therapeutic application of its different components. The objective of this study was to produce -venom-loaded cross-linked chitosan nanoparticles (Tsv/CN) at concentrations of 0.5% and 1.0% to improve their biological antimicrobial activity. Polymeric nanoparticles were formed with a homogeneous particle size and spherical shape. Experimental formulation parameters were verified in relation to mean size (<180 nm), zeta potential, polydispersity index and encapsulation efficiency (>78%). Tsv/CN 1.0% demonstrated an ability to increase the antimicrobial venom effect against bacteria, exhibiting an MIC value of 44.6 μg/mL. It also inhibited different yeast species of the genus, and Tsv/CN 0.5% and 1.0% led to a greater inhibitory effect of and strains, presenting MIC values between 22.2 and 5.5 µg/mL, respectively. These data demonstrate the biotechnological potential of these nanosystems to obtain a new therapeutic agent with potential antimicrobial activity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11432167PMC
http://dx.doi.org/10.3390/ijms25189893DOI Listing

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