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Photoinactivation of multidrug resistant bacteria by monomeric methylene blue conjugated gold nanoparticles. | LitMetric

Photoinactivation of multidrug resistant bacteria by monomeric methylene blue conjugated gold nanoparticles.

J Photochem Photobiol B

Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002, India. Electronic address:

Published: September 2017

AI Article Synopsis

  • Multidrug resistant (MDR) bacterial infections are rising due to increased antibiotic resistance, posing a significant public health threat.
  • Researchers have developed a method using Concanavalin-A directed dextran capped gold nanoparticles (GNP-ConA) to enhance the effectiveness and selectivity of methylene blue (MB) photodynamic therapy against MDR bacteria like E. coli and Klebsiella pneumoniae.
  • This treatment demonstrates high efficacy with 97% bacterial killing, minimal toxicity to mammalian cells, and operates through a specific photochemical mechanism, suggesting it could be a promising strategy for combating MDR infections.

Article Abstract

Multidrug resistant (MDR) bacterial infections have become a severe threat to the community health due to a progressive rise in antibiotic resistance. Nanoparticle-based photodynamic therapy (PDT) is increasingly been adopted as a potential antimicrobial option, yet the cytotoxicity associated with PDT is quite unspecific. Herein, we show Concanavalin-A (ConA) directed dextran capped gold nanoparticles (GNP-ConA) enhanced the efficacy and selectivity of methylene blue (MB) induced killing of multidrug resistant clinical isolates. Here, we show that our complex MB@GNP-ConA is effective against range of MDR clinical isolates, including Escherichia coli, Klebsiella pneumoniae and Enterobacter cloacae. In our treatment modality negligible dark toxicity suggests photochemically driven process with 97% killing of MDR bacteria. GNP-ConA with monomeric form of MB departs maximum fluorescence decay time (τf: 1.7ns in HSA) and singlet oxygen (ΔΦ; 0.84) for improved activity in albumin rich infection sites. Further, the complex show least toxicity when tested against HEK293 mammalian cells. The principle component analysis (PCA) and confocal microscopy illustrates cytosolic O mediated type-II PDT as mechanism of action. Hence, MB@GNP-ConA mediated PDT is potential therapeutic approach against MDR infections and can be tailored to fight other infectious diseases.

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Source
http://dx.doi.org/10.1016/j.jphotobiol.2017.07.011DOI Listing

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