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1.
J Food Sci ; 82(5): 1132-1141, 2017 May.
Article in English | MEDLINE | ID: mdl-28425569

ABSTRACT

Nanoencapsulation can provide a means to effectively deliver antimicrobial compounds and enhance the safety of fresh produce. However, to date there are no studies which directly compares how different nanoencapsulation systems affect fresh produce safety and quality. This study compared the effects on quality and safety of fresh-cut lettuce treated with free and nanoencapsulated natural antimicrobial, cinnamon bark extract (CBE). A challenge study compared antimicrobial efficacy of 3 different nanoencapsulated CBE systems. The most effective antimicrobial treatment against Listeria monocytogenes was chitosan-co-poly-N-isopropylacrylamide (chitosan-PNIPAAM) encapsulated CBE, with a reduction on bacterial load up to 2 log10 CFU/g (P < 0.05) compared to the other encapsulation systems when fresh-cut lettuce was stored at 5 °C and 10 °C for 15 d. Subsequently, chitosan-PNIPAAM-CBE nanoparticles (20, 40, and 80 mg/mL) were compared to a control and free CBE (400, 800, and 1600 µg/mL) for its effects on fresh-cut lettuce quality over 15 d at 5 °C. By the 10th day, the most effective antimicrobial concentration was 80 mg/mL for chitosan-PNIPAAM-CBE, up to 2 log10 CFU/g reduction (P < 0.05), compared with the other treatments. There was no significant difference between control and treated samples up to day 10 for the quality attributes evaluated. Chitosan-PNIPAAM-CBE nanoparticles effectively inhibited spoilage microorganisms' growth and extended fresh-cut lettuce shelf-life. Overall, nanoencapsulation provided a method to effectively deliver essential oil and enhanced produce safety, while creating little to no detrimental quality changes on the fresh-cut lettuce.


Subject(s)
Acrylic Resins , Anti-Infective Agents/administration & dosage , Chitosan , Food Microbiology , Lactuca/microbiology , Nanocapsules/chemistry , Oils, Volatile/administration & dosage , Anti-Infective Agents/pharmacology , Colony Count, Microbial , Food Safety , Humans , Listeria monocytogenes/growth & development , Oils, Volatile/pharmacology , Plant Extracts/administration & dosage , Plant Extracts/pharmacology , Safety , Vegetables/microbiology
2.
J Food Sci ; 78(12): N1913-20, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24329956

ABSTRACT

Previous studies have reported antimicrobial and antioxidant activity of black pepper oleoresin which is associated to its phenolic compounds and piperine. The ability of cyclodextrins to form an inclusion complex with a guest molecule could improve black pepper oleoresin application, bioavailability, and stability in foods. Hydroxypropyl beta-cyclodextrin (HPBCD) inclusion complex with black pepper olereosin were synthesized using the kneading method and characterized for its physico-chemical properties and its antioxidant and antimicrobial activities. Inclusion complex size was 103.9 ± 7.6 nm and indicated to be a polydisperse system. The entrapment efficiency was 78.3 ± 3.6%, which suggests that other constituents in black pepper oleoresin have higher affinities for HPBCD than piperine (major compound in black pepper oleoresin). Thermograms showed the disappearance of oxidation peaks of black pepper oleoresin, proving complex formation with HPBCD. Phase solubility results indicated 1:1 stoichiometric inclusion complex formation and an increase of black pepper oleoresin aqueous solubility with HPBCD concentration. Nano-encapsulation with HPBCD did not affect (P > 0.05) total phenolic content; however, it enhanced (P < 0.05) black pepper oleoresin antioxidant activity. Black pepper oleoresin and its inclusion complex were analyzed for their antimicrobial activity against Escherichia coli K12 and Salmonella enterica serovar Typhimurium LT2. Both free and encapsulated black pepper oleoresin effectively inhibited bacterial growth within the concentration range tested. Black pepper oleoresin encapsulated in HPBCD was able to inhibit Salmonella at lower (P < 0.05) concentrations than its corresponding free extract. Therefore, black pepper oleoresin-HPBCD nanocapsules could have important applications in the food industry as antimicrobial and antioxidant system.


Subject(s)
Anti-Infective Agents/chemistry , Antioxidants/chemistry , Nanotechnology/methods , Piper nigrum/chemistry , Plant Extracts/chemistry , 2-Hydroxypropyl-beta-cyclodextrin , Anti-Infective Agents/pharmacology , Antioxidants/pharmacology , Calorimetry, Differential Scanning , Cyclodextrins/chemistry , Escherichia coli K12/drug effects , Food Contamination/prevention & control , Food Microbiology , Food Technology , Nanoparticles/chemistry , Particle Size , Phenols/chemistry , Phenols/pharmacology , Plant Extracts/pharmacology , Salmonella/drug effects , Solubility , Water/analysis , beta-Cyclodextrins/chemistry
3.
J Food Sci ; 78(4): N626-32, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23464835

ABSTRACT

Nanoencapsulation of active compounds using poly-(d,l-lactide-co-glycolide) (PLGA) is commonly used in the pharmaceutical industry for drug delivery and may have important applications in the food industry. Control of growth of foodborne bacteria with the goals of reducing the number of foodborne illness outbreaks, assuring consumers a safer food supply remains a priority in the food industry. Natural antimicrobials are an excellent way to eliminate pathogens without introducing chemical preservatives that consumers may find undesirable. Cinnamon bark extract (CBE) is an effective pathogen inhibitor isolated from cinnamon spice. PLGA nanoparticles containing CBE were produced using an emulsion-solvent evaporation method and characterized for size, polydispersity, morphology, entrapment efficiency, in vitro release and pathogen inhibition. PLGA with 2 different ratios of lactide to glycolide (65:35 and 50:50) were used to determine how polymer composition affected nanoparticle characteristics and antimicrobial potency. The size of the nanoparticles ranged from 144.77 to 166.65 nm and the entrapment efficiencies of CBE in 65:35 PLGA and 50:50 PLGA were 38.90% and 47.60%, respectively. The in vitro release profile at 35 °C showed an initial burst effect for both types of PLGA followed by a more gradual release of CBE from the polymer matrix. Both types of PLGA nanoparticles loaded with CBE were effective inhibitors of Salmonella enterica serovar Typhimurium and Listeria monocytogenes after 24 and 72 h at concentrations ranging from 224.42 to 549.23 µg/mL. The PLGA encapsulation improved delivery of hydrophobic antimicrobial to the pathogens in aqueous media.


Subject(s)
Anti-Infective Agents/pharmacology , Cinnamomum zeylanicum/chemistry , Lactic Acid/pharmacology , Listeria monocytogenes/drug effects , Nanoparticles/chemistry , Plant Extracts/pharmacology , Polyglycolic Acid/pharmacology , Salmonella typhimurium/drug effects , Anti-Infective Agents/chemistry , Chemical Phenomena , Delayed-Action Preparations , Emulsions , Lactic Acid/chemistry , Particle Size , Plant Bark/chemistry , Plant Extracts/chemistry , Polyglycolic Acid/chemistry , Polylactic Acid-Polyglycolic Acid Copolymer , Solvents/chemistry
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