AI Article Synopsis

  • Antimicrobial photodynamic therapy (aPDT) uses light-activated compounds to target and kill drug-resistant bacteria, particularly in aquaculture settings.
  • Two clinical isolates of Gram-negative bacteria were tested: one resistant (R) and one sensitive (S) to treatment, impacting fish farming significantly due to antibiotic ineffectiveness.
  • The study evaluated different forms of palladium phthalocyanines and zinc phthalocyanine, with promising results suggesting aPDT as a viable alternative to traditional antibiotics for controlling harmful pathogens.

Article Abstract

Antimicrobial photodynamic therapy (aPDT) has been considered as a promising methodology to fight the multidrug resistance of pathogenic bacteria. The procedure involves a photoactive compound (photosensitizer), the red or near infrared spectrum for its activation, and an oxygen environment. In general, reactive oxygen species are toxic to biomolecules which feature a mechanism of photodynamic action. The present study evaluates two clinical isolates of Gram-negative (): a multidrug resistant (R) and a sensitive (S) strain. Both occur in farmed fish, leading to the big production losses because of the inefficacy of antibiotics. Palladium phthalocyanines (PdPcs) with methylpyridiloxy groups linked peripherally (pPdPc) or non-peripherally (nPdPc) were studied with full photodynamic inactivation for 5.0 µM nPdPc toward both , R and S strains (6 log), but with a half of this value (3 log) for 5.0 µM pPdPc and only for , S. In addition to the newly synthesized PdPcs as a "positive control" was applied a well-known highly effective zinc phthalocyanine (ZnPcMe). ZnPcMe showed optimal photocytotoxicity for inactivation of both R and S. The present study is encouraging for a further development of aPDT with phthalocyanines as an alternative method to antibiotic medication to keep under control the harmful pathogens in aquacultures' farms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164046PMC
http://dx.doi.org/10.3390/cimb44050133DOI Listing

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