Ceftizoxime loaded ZnO/l-cysteine based an advanced nanocarrier drug for growth inhibition of Salmonella typhimurium

l -Cysteine coated zinc oxide (ZnO) nano hollow spheres were prepared as a potent drug delivery agent to eradicate Salmonella enterica serovar Typhimurium ( S. typhimurium ). The ZnO nano hollow spheres were synthesized by following the environmentally-friendly trisodium citrate assisted method and...

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Veröffentlicht in:Scientific reports 2021-07, Vol.11 (1), p.15565-15565, Article 15565
Hauptverfasser: Bacchu, M. S., Ali, M. R., Setu, M. A. A., Akter, S., Khan, M. Z. H.
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Sprache:eng
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Zusammenfassung:l -Cysteine coated zinc oxide (ZnO) nano hollow spheres were prepared as a potent drug delivery agent to eradicate Salmonella enterica serovar Typhimurium ( S. typhimurium ). The ZnO nano hollow spheres were synthesized by following the environmentally-friendly trisodium citrate assisted method and l -cysteine (L-Cys) conjugate with its surface. ZnO/L-Cys@CFX nanocarrier drug has been fabricated by incorporating ceftizoxime with L-Cys coated ZnO nano hollow spheres and characterized using different techniques such as scanning electron microscope (SEM), attenuated total reflection Fourier transform infrared (ATR-FTIR), and X-ray diffraction (XRD) etc. Furthermore, the drug-loading and encapsulation efficiency at different pH levels was measured using UV–vis spectrometer and optimized. A control and gradual manner of pH-sensitive release profile was found after investigating the release profile of CFX from the carrier drug. The antibacterial activity of ZnO/L-Cys@CFX and CFX were evaluated through the agar disc diffusion method and the broth dilution method, which indicate the antibacterial properties of antibiotics enhance after conjugating. Surprisingly, the ZnO/L-Cys@CFX exhibits a minimum inhibitory concentration (MIC) of 5 µg/ml against S. typhimurium is lower than CFX (20 µg/ml) itself. These results indicate the nanocarrier can reduce the amount of CFX dosed to eradicate S. typhimurium .
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-021-95195-0