Development of Edible Bioactive Coating Based On Modified Chitosan For Increasing PDF
Development of Edible Bioactive Coating Based On Modified Chitosan For Increasing PDF
Development of Edible Bioactive Coating Based On Modified Chitosan For Increasing PDF
a r t i c l e i n f o a b s t r a c t
Article history: For increasing the shelf life of strawberries during storage, bioactive coatings were applied using modified
Received 23 August 2010 polysaccharides of chitosan. First, antimicrobial tests were performed with selected essential oils to evaluate
Accepted 22 October 2010 their antimicrobial capacities against moulds and total flora isolated from strawberries. Red thyme (RT) and
oregano extract (OR) were found as strong bioactive agents against moulds and total flora isolated from
Keywords:
strawberries, whereas limonene (LIM) and peppermint (PM) had lower antimicrobial properties. These
Bioactive coating
Chitosan
essential oils were also used as bioactive compounds which were sprayed onto strawberries and evaluated for
Essential oils their potential to increase shelf life during storage at 4 °C. RT, PM and LIM were found to be more efficient
Limonene preservative agents for strawberries during 14 days of storage. Finally, chitosan was functionalized by
Strawberries acylation with palmitoyl chloride to increase its hydrophobicity, to ensure a controlled release and improve its
Shelf life stability and adhesion to the fruit product. LIM and PM were incorporated into the modified chitosan to create
bioactive edible coatings and these were tested for their ability to extend the shelf life of fresh strawberries
during storage. Formulations based on modified chitosan containing LIM and Tween®80 were shown to
perform better than other formulations.
© 2010 Elsevier Ltd. All rights reserved.
1. Introduction Wang, Li & Liu, 2007). Therefore, finding suitable methods for
preserving the quality of strawberries during storage is important.
Strawberries are especially perishable fruits, being susceptible to The use of edible coatings represents one of the important
mechanical injury, desiccation, decay and physiological disorders methods being used for preserving quality. Edible coatings have
during storage. Tournas and Katsoudas (2005) have examined mould been traditionally used to improve food appearance and maintain
and yeast growth in strawberries in order to isolate and identify the quality because they are considered environmentally friendly
predominant species infecting fruits following surface disinfection (Khwaldia, Perez, Banon, Desobry & Hardy, 2004). Coating films can
and incubation at room temperature over 14 days. Botrytis cinerea and act as barriers to moisture and oxygen during processing, handling
Rhizopus stolonifer were the two major storage pathogens observed in and storage (Xu et al., 2007). Moreover, they can retard food
strawberries. Their high level of contamination, as compared to other deterioration by inhibiting the growth of microorganisms, due to
type of fruits, was mainly due to a lower pH, an optimal water activity their natural intrinsic activity or to the incorporation of antimicrobial
for fungal growth, high levels of sugars and other nutrients, and a soft compounds (Cha & Chinnan, 2004). Normally, edible films are made of
skin that can be easily ruptured, favoring microorganism proliferation. proteins or polysaccharides that can also help to maintain moisture,
B. cinerea (grey mould rot) is a ubiquitous pathogen which causes thereby improving shelf life. However, the hydrophilic nature of these
severe damage in many fruits, vegetables and ornamental crops both compounds limits their ability to provide desired edible film
pre- and post-harvest. The pathogen infects leaves, stems, flowers and functions. Current approaches to extend functional and mechanical
fruits (Bouchra, Achouri, Idrissi Hassani & Hmamouchi, 2003) and is a properties of these films include (i) incorporation of hydrophobic
major obstacle to long-distance transport and storage (Xu et al., compounds such as lipids to improve their resistance to water
2007). R. stolonifer is the causal agent of Rhizopus rot disease of various (McHugh & Krochta, 1994), (ii) optimization of the interaction
fruits and vegetables. This fungus primarily infects ripe fruit only after between polymers (protein-protein interactions, charge–charge
harvest unless the fruit in the field has major injuries (Zhang, Zheng, electrostatic complexes between proteins or polysaccharides) and
(iii) cross-linking or functionalization through physical, chemical, or
enzymatic treatments (Pierro et al., 2006).
Furthermore, it has been demonstrated that bioactive compounds
⁎ Corresponding author. Tel.: + 1 450 687 5010; fax: + 1 450 686 5501. such as essential oils (EOs) can be added to such coatings in order to
E-mail address: monique.lacroix@iaf.inrs.ca (M. Lacroix). lengthen shelf life, to prevent microorganism growth and to preserve
0963-9969/$ – see front matter © 2010 Elsevier Ltd. All rights reserved.
doi:10.1016/j.foodres.2010.10.037
K.D. Vu et al. / Food Research International 44 (2011) 198–203 199
nutritional values of foods (Salmieri & Lacroix, 2006; Vargas, Albors, bag containing 225 ml of sterile peptoned water and homogenized for
Chiralt & González-Martínez, 2009). EOs have been found to exhibit 2 min using a Lab blender 400 stomacher (Laboratory Equipment,
antimicrobial and antifungal properties, making them as natural London, UK). The obtained mixture was serially diluted, then plated
alternatives to combat foodborne pathogens and normal food decay on acidified Potato Dextrose Agar (PDA, pH 3.5) and incubated at
caused by bacterial and mould growth (Lacroix, 2007). The immobili- 25 °C for 72 h. Mould colonies were isolated and inoculated in a flask
zation of the active compounds in polymer can maintain high containing 36 ml of sterilized Potato Dextrose Broth (PDB), then, the
concentrations of the active compounds on the surface of foods in flask was incubated at 25 °C for 48 h. At the end of incubation, sterile
order to achieve a longer storage time (Ouattara, Sabato & Lacroix, 2001). glycerol was added into the flask to obtain a final glycerol
Chitosan is a cationic polysaccharide obtained from partial deace- concentration of 20% (w/v) and aliquots of 1 ml of the mixture were
tylation of chitin, the main constituent of the crustacean skeleton divided into cryovials and frozen at -80 °C for future utilization.
(Rinaudo & Domard, 1989). This polymer is non-toxic, biodegradable Isolation of total flora: in sterile conditions, 25 g of fresh
and biocompatible (Shapiro & Cohen, 1997), and is also easily modified strawberries (no sign of disease and visual decay) was placed in a
by physical or chemical methods (Le Tien, Lacroix, Ispas-Szabo & bag containing 225 ml of sterile peptoned water and homogenized for
Mateescu, 2003). It is widely used in encapsulation applications due to 6 min using a stomacher. A volume of 1 ml of homogenized mixture
its ability to form gels in the presence of certain divalent cations such as was inoculated in a flask containing 36 ml of sterilized Tryptic Soy
calcium, barium and strontium by ionotropic gelation (Braccini & Perez, Broth (TSB) and incubated at 37 °C for 24 h. At the end of incubation,
2001; Ramadas, Paul, Dileep, Anitha & Sharma, 2000). A new sterile glycerol was added into the flask to achieve a final glycerol
formulation based on acylation with fatty acid derivatives was concentration of 20% (w/v) and aliquots of 1 ml of the mixture were
elaborated on chitosan to enhance the hydrophobic properties of the divided into cryovials and frozen at − 80 °C for future utilization.
polymers (Han, Guenier, Salmieri & Lacroix, 2008). Consequently, the Before each experiment, stock cultures were propagated through 2
encapsulated substances in chitosan-based beads could be protected consecutive growth cycles: (i) in PDB for total moulds at 25 °C for 72 h
against moisture and the controlled release mechanism was improved and (ii) in TSB for total flora at 37 °C for 24 h. The fermented broths
(Han et al., 2008; Le Tien et al., 2003). were centrifuged at 1500×g for 10 min at 4 °C. The obtained pellets
Thus, the objective of this study was to develop an active edible were washed twice with sterile saline water (0.85%, w/v) and then
coating formulation in order to increase the shelf life of fresh food diluted to have working cultures with approximately 108 CFU/ml.
products. Strawberries were used as a model for the application of edible
coatings. First, an inhibitory in vitro test (antimicrobial assay) was
2.2.2. Antimicrobial assay
performed with selected antifungal natural compounds in order to
LIM, OR, RT, PM, and LG were used to evaluate their inhibition
evaluate their antimicrobial capacities against moulds and total flora
potential against the growth of total flora and total moulds by paper
isolated from strawberries. Second, antimicrobial compounds were
disk method (Bona da Silva, Guterres, Weisheimer & Schapoval,
evaluated as emulsion-based coatings for their specific antifungal
2008). Tryptic soy Agar (TSA) and acidified PDA plates were
properties on fresh strawberries. Finally, functionalized polymer of
thoroughly inoculated with the working cultures of total flora and
chitosan was synthesized. Then, the antimicrobial coatings using
total moulds. A paper disk was placed in the middle of the plate except
functionalized chitosan, containing limonene and peppermint in
for the control plates which received no treatment. A volume of 5 μl of
presence of an emulsifier was developed to increase the shelf life of
antifungal agent (0.02%, w/v) was then added to the paper disk and
strawberries.
incubated at 37 °C for 24 in case of TSA plates and at 25 °C for 48 h in
case of acidified PDA plates. The test was conducted in triplicate for
2. Materials and methods
each sample. The test ended when the control plates were fully
covered by bacteria or moulds and the inhibition radius of paper disk
2.1. Materials
was measured and expressed as mm of inhibition.
Fresh strawberries were bought from a local supermarket (IGA,
Laval, Quebec, Canada) and were inspected for no sign of disease and 2.3. Evaluation of antimicrobial compounds on the shelf life of strawberries
visual decay.
Limonene (LIM) was from Sigma-Aldrich Ltd. (Oakville, Ontario, A shelf life study was conducted to verify the effect of selected
Canada). Oregano (OR; Oreganum compactum) essential oil was from antifungal compounds (LIM, LG, PM, RT and OR) on the growth of
Robert & Fils (Montreal, QC, Canada). Red thyme (RT; Thymus moulds (R. Stolonifer and B. cinerea) on strawberries during storage at
vulgaris), peppermint (PM; Mentha piperita) and lemongrass (LG; 4 °C. Prior to use, the essential oils were passed through a 0.2 μm filter
Cymbopogon citrates) essential oils were from BSA (Montreal, QC, to ensure sterility. Concentrations of 0.2% essential oil with 0.4%
Canada). Tween®80 were used to prepare coating emulsions in aqueous phase
Chitosan (Kitomer™, Mw 1600 kDa, 85–89% deacetylation degree) under vigorous stirring using an IKA® T25 digital Ultra-Turrax
was obtained from Marinard Biotech Inc. (Rivière-aux-Renards, QC, disperser (IKA® Works Inc.) for 10 min at room temperature to
Canada). Palmitoyl chloride was from Fluka Biochemika (Buchs, obtain a final concentration of 0.02% antifungal compounds.
Switzerland). The other reagents were purchased from Laboratoire The strawberries were separated into 6 groups with 20 strawberries
MAT (Beauport, QC, Canada) and used without further purification. per group: (i) control (uncoated); (ii) coated with LIM; (iii) coated with
LG; (iv) coated with OR; (v) coated with PM; and (vi) coated with RT.
2.2. Evaluation of growth inhibition of antimicrobial compounds on total These groups were placed on sterile aluminum foil-covered trays. The
flora and moulds by antimicrobial assay coatings suspensions were sprayed onto fresh strawberries in sterile
conditions (under a biological containment hood) at room temperature.
An antimicrobial assay was performed on selected antifungal Each side of each strawberry was sprayed twice (fully cover by coating
agents to evaluate their effect on the growth of total flora and moulds suspensions). After spraying, strawberries were allowed to dry for
isolated from strawberries. 15 min on sterile aluminum sheets. Then, the strawberries were covered
using a second sterile aluminum sheet and were stored at 4 °C. Visual
2.2.1. Isolation of total flora and moulds decay of strawberries was evaluated for 14 days (day 0 corresponded to
Isolation of total moulds: in sterile conditions, 25 g of fresh the day of the treatment) and the mould contamination percentage
strawberries (no sign of disease and visual decay) was placed in a (defined as the percentage of strawberries that showed the presence of
200 K.D. Vu et al. / Food Research International 44 (2011) 198–203
one or more white colonies (R. stolonifer) or dark brown multi-celled Table 1
colonies (B. cinerea)) was calculated during storage. Antimicrobial activity against total flora and moulds isolated from strawberries.
Acknowledgments
References
Bona da Silva, C., Guterres, S. S., Weisheimer, V., & Schapoval, E. E. S. (2008). Antifungal
Fig. 2. Mould contamination percentage in strawberries coated with modified chitosan activity of the lemongrass oil and citral against Candida spp. The Brazilian Journal of
containing limonene and peppermint and emulsifier during storage at 4 °C. Infectious Diseases, 12, 63−66.
K.D. Vu et al. / Food Research International 44 (2011) 198–203 203
Bouchra, C., Achouri, M., Idrissi Hassani, L. M., & Hmamouchi, M. (2003). Chemical Mahboubi, M., & Haghi, G. (2008). Antimicrobial activity and chemical composition of
composition and antifungal activity of essential oils of seven Moroccan Labiatae Mentha pulegium L. essential oil. Journal of Ethnopharmacology, 119, 325−327.
against Botrytis cinerea Pers: Fr. Journal of Ethnopharmacololy, 89, 165−169. McHugh, T. H., & Krochta, J. M. (1994). Milk-protein-based edible films and coatings.
Braccini, I., & Perez, I. (2001). Molecular basis of Ca++-induced gelation in alginate and Food Technolology, 48, 97−103.
pectin: The egg-box model revisited. Biomacromolecules, 2, 1089−1096. Mazur, S., & Waksmundzka, A. (2001). Effect of some compounds on the decay of
Bupesh, G., Amutha, C., Nandagopal, S., Ganeshkumar, A., Sureshkumar, P., & Saravana strawberry fruits caused by Botrytis cinerea Pers. Meded Rijksuniv Gent Fak
Murali, K. (2007). Antibacterial activity of Mentha piperita L. (peppermint) from Landbouwkd Toegep Biol Wet, 66, 227−231.
leaf extracts – A medicinal plant. Acta Agriculturae Slovenica, 89, 73−79. Ouattara, B., Sabato, S. F., & Lacroix, M. (2001). Combined effect of antimicrobial coating
Cha, D. S., & Chinnan, M. S. (2004). Biopolymer-based antimicrobial packaging: A and gamma irradiation on shelf life extension of pre-cooked shrimp (Penaeus spp.).
review. Critical Review in Food Science and Nutrition, 44, 223−237. International Journal of Food Microbiolology, 68, 1−9.
Chao, S. C., Young, G. D., & Oberg, C. J. (2000). Screening of inhibitory activity of essential oils on Pierro, P. D., Chico, B., Villalonga, R., Mariniello, L., Damiao, A. E., Masi, P., et al.
selected bacteria, fungi, and viruses. Journal of Essential Oil Research, 12, 639−649. (2006). Chitosan-Whey protein edible films produced in the absence or
Curtis, O. F., Shetty, K., Cassagnol, G., & Peleg, M. (1996). Comparison of the inhibitory presence of transglutaminase: Analysis of their mechanical and barrier
and lethal effects of synthetic versions of plant metabolites (anethole, carvacrol, properties. Biomacromolecules, 7, 744−749.
eugenol and thymol) on a food spoilage yeast (Debaromyces hansenii). Food Ramadas, M., Paul, W., Dileep, K. J., Anitha, Y., & Sharma, C. P. (2000). Lipoinsulin
Biotechnology, 10, 55−73. encapsulated alginate-chitosan capsules: Intestinal delivery in diabetic rats. Journal
Dambolena, J. S., Lopéz, A. G., Canepa, M. C., Theumer, M. G., Zydadlo, J. A., & Rubinstein, of Microencapsulation, 17, 405−411.
H. A. (2008). Inhibitory effect of cyclic terpenes (limonene, menthol, menthone and Reddy, M. V. B., Angers, P., Gosselin, A., & Arul, J. (1998). Characterization and use of
thymol) on Fusarium verticillioides MRC 826 growth and fumonisin B1 biosynthesis. essential oil from Thymus vulgaris against Botrytis cinerea and Rhizopus stolonifer in
Toxicon, 51, 37−44. strawberry fruits. Phytochemistry, 47, 1515−1520.
Edris, A. E., & Farrag, E. S. (2003). Antifungal activity of peppermint and sweet basil Rinaudo, M., & Domard, A. (1989). Solution properties of chitosan. In G. Skjak-Braek, T.
essential oils and their major aroma constituents on some plant pathogenic fungi Anthonsen, & P. Sandford (Eds.), Chitin and chitosan (pp. 71−83). New York: Elsevier.
from the vapor phase. Nahrung/Food, 47, 117−121. Salmieri, S., & Lacroix, M. (2006). Physicochemical properties of alginate/
Ernestina, A., Miguel, A. M., Maria, M. H., Socorro, V., Eduardo, P., & Irasema, V. (2003). polycaprolactone-based films containing essential oils. Journal of Agricultural
Fungicidal potential of methoxylated flavones from citrus for in vitro control of and Food Chemistry, 54, 10205−10214.
Colletotrichum gloeosporioides, causal agent of anthracnose disease in tropical fruits. Shapiro, L., & Cohen, S. (1997). Novel alginate sponges for cell culture and
Pest Management Science, 59, 1245−1249. transplantation. Biomaterials, 18, 583−590.
Han, J., Guenier, A. -S., Salmieri, S., & Lacroix, M. (2008). Alginate and chitosan Sharma, N., & Tripathi, A. (2008). Effects of Citrus sinensis (L.) Osbeck epicarp essential
functionalization for micronutrient encapsulation. Journal of Agricultural and Food oil on growth and morphogenesis of Aspergilus niger (L.) Van Tieghem.
Chemistry, 56, 2528−2535. Microbiological Research, 163, 337−344.
Inouye, S., Takizawa, T., & Yamaguchi, H. (2001). Antibacterial activity of essential oils Singh, P., Shukla, R., Prakash, B., Kumar, A., Singh, S., Mishra, P. K., et al. (2010). Chemical
and their major constituents against respiratory tract pathogens by gaseous profile, antifungal, antiaflatoxigenic and antioxidant activity of Citrus maxima
contact. The Journal of Antimicrobial Chemotherapy, 47, 565−573. Burm. and Citrus sinensis (L.) Osbeck essential oils and their cyclic monoterpene,
Janssen, A. M., Chin, N. M., Scheffer, J. J. C., & Baerheim Svendsen, A. (1986). Screening DL-limonene. Food and Chemical Toxicology, 48, 1734−1740.
for antimicrobial activity of some essential oils by the agar overlay technique. Skandamis, P., Tsigarida, E., & Nychas, G. J. E. (2000). Ecophysiological attributes of Salmonella
Statistics and correlations. Pharmacy World and Science, 8, 289−292. typhimurium in liquid culture and within a gelatin gel with or without the addition of
Jirovetz, L., Buchbauer, G., Stoyanova, A. S., Evgenii, V., Georgie, V., & Damianova, T. oregano essential oil. World Journal of Microbiology & Biotechnology, 16, 31−35.
(2003). Composition, quality control and antimicrobial activity of the essential oil Tournas, V. H., & Katsoudas, E. (2005). Mould and yeast flora in fresh berries, grapes and
long time stored dill (Anethum graveolens L.) seeds from Bulgaria. Journal of citrus fruits. International Journal of Food Microbiology, 105, 11−17.
Agricultural and Food Chemistry, 51, 3854−3857. USEPA. (1994). Registration eligibility decision (RED): Limonene. Washington D.C, USA.
Khwaldia, K., Perez, C., Banon, S., Desobry, S., & Hardy, J. (2004). Milk proteins for edible Vargas, M., Albors, A., Chiralt, A., & González-Martínez, C. (2009). Characterization of
films and coatings. Critical Review in Food Science and Nutrition, 44, 239−251. chitosan-oleic acid composite films. Food Hydrocolloids, 23, 536−547.
Kim, J., Marshall, M. R., & Wei, C. I. (1995). Antibacterial activity of some essential oil Wilson, C. L., Solar, J. M., El Ghaouth, A., & Wisniewski, M. E. (1997). Rapid evalution of
component against five foodborne pathogens. Journal of Agricultural and Food plant extracts and essential oils for antifungal activity against Botrytis cinerea. Plant
Chemistry, 43, 2839−2845. Disease, 81, 204−210.
Lacroix, M. (2007). The use of essential oils and bacteriocins as natural antimicrobial Xu, W. T., Huang, K. L., Guo, F., Qu, W., Yang, J. J., Liang, Z. H., et al. (2007). Postharvest
and antioxidant compounds. Food, 1, 181−192. grapefruit seed extract and chitosan treatments of table grapes to control Botrytis
Larmond, E. (1979). Laboratory methods for sensory evaluation of food. : Canadian cinerea. Postharvest Biolology and Technology, 46, 86−94.
Government Publishing Centre. Zhang, H., Zheng, X., Wang, L., Li, S., & Liu, R. (2007). Effect of yeast antagonist in
Le Tien, C., Lacroix, M., Ispas-Szabo, P., & Mateescu, M. A. (2003). N-acylated chitosan: combination with hot water dips on postharvest Rhizopus rot of strawberries.
Hydrophobic matrices for controlled drug release. Journal of Controlled Release, 93, 1−13. Journal of Food Engineering, 78, 281−287.