2018
DOI: 10.3389/fsufs.2018.00004
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Geraniol-Loaded Polymeric Nanoparticles Inhibit Enteric Pathogens on Spinach during Posttreatment Refrigerated and Temperature Abuse Storage

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Cited by 12 publications
(22 citation statements)
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“…We are not surprised by the observed differences in spinach decontamination outcomes for the GPN and HOCl treatments, given our previous published research on antimicrobial-loaded nanoparticles applied to decontaminate spinach (Perez-Lewis et al, 2018;Ruengvisesh et al, 2019a). Finally, the current study details the capability of the plant-derived antimicrobial geraniol, free and encapsulated within polymeric micelles, to reduce the numbers of inoculated E. coli O157:H7 and S. Typhimurium on spinach leaves during a simulated multicontamination spinach production and post-harvest handling scenario.…”
Section: Discussionmentioning
confidence: 73%
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“…We are not surprised by the observed differences in spinach decontamination outcomes for the GPN and HOCl treatments, given our previous published research on antimicrobial-loaded nanoparticles applied to decontaminate spinach (Perez-Lewis et al, 2018;Ruengvisesh et al, 2019a). Finally, the current study details the capability of the plant-derived antimicrobial geraniol, free and encapsulated within polymeric micelles, to reduce the numbers of inoculated E. coli O157:H7 and S. Typhimurium on spinach leaves during a simulated multicontamination spinach production and post-harvest handling scenario.…”
Section: Discussionmentioning
confidence: 73%
“…The current study sought to evaluate the produce surfacesanitizing utility of an innovative antimicrobial treatment composed of polymeric nanoparticles loaded with the PDA geraniol, as well as free geraniol and 200 ppm free chlorine, in a scenario involving multiple sequential spinach contamination events. In previous research, identically-prepared GPNs prevented growth of these organisms on spinach surfaces during refrigerated and temperature abuse storage, and showed capacity to inhibit pathogen growth when applied prior to pathogen inoculation (Perez-Lewis et al, 2018). Figure 2A depicts the size distribution of GPNs via DLS analysis, and indicates a mean particle size of 416.5 ± 77.9 nm.…”
Section: Resultsmentioning
confidence: 79%
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“…To selectively/differentially enumerate pathogens, samples were placed in stomacher bags and pummeled (230 rpm) with 99 ml sterile 0.1% (wt/vol) peptone diluent for 1.0 min. Surviving pathogens were serially diluted in 9.0 ml sterile 0.1% peptone diluent and then spread on surfaces of lactose‐sulfite‐phenol red‐rifampicin agar supplemented with 100.0 μg/ml rifampicin according to methods previously published (Perez, Lucia, Cisneros‐Zevallos, Castillo, & Taylor, ; Perez‐Lewis et al, ). The limit of detection for plating assays was 100 cfu/30 cm 2 (0.5 log 10 cfu/cm 2 ).…”
Section: Methodsmentioning
confidence: 99%