毕业论文外文翻译-基于壳聚糖包埋茶多酚活性膜的制备与表征.docx

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1、Preparation and characterization of active films based on chitosanincorporated tea polyphenolsAbstract:Active films based on chitosan incorporated tea polyphenols with different concentrations were developed. Attenuated total reflectance Fourier transform infrared spectrometry was used to investigat

2、e the potential interactions between chitosan and tea polyphenols in the films. Physical properties of the chitosan films incorporated tea polyphenols, including density, moisture content, opacity, color, water solubility and water vapor permeability, were measured. Antioxidant activity of the films

3、 was characterized in terms of total phenolic content and 2, 2-diphenyl-1-picrylhydrazyl free radical scavenging activity. The results indicated that the incorporation of tea polyphenols caused interactions between chitosan and tea polyphenols and gave rise to the films darker appearance. After the

4、addition of tea polyphenols, the films showed increased water solubility and decreased water vapor permeability. Meanwhile, the incorporation of tea polyphenols enhanced the total phenolic content and 2, 2-diphenyl-1-picrylhydrazyl free radical scavenging activity of the films, i.e., increased the a

5、ntioxidant activity of the films. But the antioxidant activity of the chitosan films incorporated tea polyphenols declined with time.1. IntroductionThere has been a growing interest in recent years to develop active packaging to improve food safety and shelf life. Principal active food packagings in

6、volve oxygen scavenging, moisture absorption, carbon dioxide or ethanol generation, and antimicrobial systems (Coma, 2008). One of the commonly used methods to develop active food packaging is to incorporate active compounds and ingredients, such as antioxidants and antimicrobial agents, into packag

7、ing materials, providing the packaging system additional functions that do not exist originally. However, concerns on consumer health and environmental issues lead researchers to develop the active food packagings based on biodegradable materials and natural substances.Chitosan, a natural carbohydra

8、te copolymer b-(1-4)-2-acetamido-a-glucose and b-(1-4)-2-amino-a-glucose units yielded from deacetylation of chitin poly-b-(1-4)-N-acetyl-2aglucosamine, is a biodegradable, non-toxic, and biocompatible polysaccharide. Due to its antimicrobial activity, chitosan has a great potential for applications

9、 in antimicrobial packaging (Aider,2010; Dutta, Tripathi, Mehrotra, & Dutta, 2009). It has been proven that chitosan based films and coatings are effective in food preservation (Portes, Gardrat, Castellan, & Coma, 2009; Vsconez, Flores, Campos, Alvarado, & Gerschenson, 2009). Functional substances,

10、such as rosemary essential oil and mint, have been incorporated into chitosan to enhance its antibacterial activity (Abdollahi, Rezaei, & Farzi, 2012; Kanatt, Chander, & Sharma, 2008a). Although chitosan is a promising biopolymer for active food packaging, it does not have significant antioxidant ac

11、tivity. Improvement of antioxidant activity of chitosan could expand its applications in active food packaging. Tea polyphenols (TP) are extracted from tea and contain catechin, flavones, anthocyan, and phenolic acid, but catechin is the main component with more than 80% content (Huang, Huang, Liu,

12、Luo, & Xu, 2007). Catechin mainly contains epigallocatechin-3-gallate (EGCG), epigallocatechin (EGC), epicatechin-3-gallate (ECG), and epicatechin (EC) (Yang, Lambert, & Sang, 2009). Research results demonstrated the antibacterial and antioxidant activities of TP, showing good prospects for their us

13、e as preservatives and antioxidants (He, Lv, & Yao, 2006). It has been showed that using TP as antioxidant or preservative could extend the shelf life of fresh mutton and fresh-cut lettuce (Kumudavally, Phanindrakumar, Tabassum, Radhakrishna, & Bawa, 2008; Martin-Diana, Rico, & Barry-Ryan, 2008). Th

14、e antioxidant mechanism of polyphenols is principally attributed to their capacity in trapping reactive oxygen species and chelating metal ions, which could generate radicals through Fenton reaction (Osman, 2011). Previous studies showed that antioxidant activity of chitosan, one of the main functio

15、ns for active food packaging, could be improved through incorporating of natural substances, such as plant extracts (Ponce, Roura, Valle, & Moreira, 2008), green tea extract (Siripatrawan & Harte, 2010), rosemary essential oil (Abdollahi et al., 2012), Zataria multiflora Boiss essential oil and grap

16、e seed extract (Moradi et al., 2012). As a good source of polyphenols, TP could be used as an antioxidant and incorporated into chitosan films or coatings. Therefore, the aim of this study was to develop environmentally friendly active films from chitosan incorporated TP with different concentration

17、s. Antioxidant activity in terms of total phenolic content and DPPH (2, 2-diphenyl-1-picrylhydrazyl) free radical scavenging activity and physical properties, including density, moisture content, opacity, color, water solubility, and water vapor permeability of the films were evaluated. 2. Material

18、and methods2.1. MaterialsChitosan with degree of deacetylation of 80e95% was supplied by Sinopharm Chemical Reagent Co. Ltd. (China). Tea polyphenols (TP) were obtained from Huzhou Rongkai Co. Ltd. (China). The TP used in this study was light yellow powder, purity99%, caffeine 0.5%, and ash 0.5%. Ca

19、techins in the TP is90%, and EGCG in the catechins is 70%. Glycerol, anhydrous CaCl2 and KNO3 were from Beijing Beihua Fine Chemicals Co. Ltd (Beijing, China). Gallic acid and FolineCiocalteu (FeC) reagent were from Shanghai Hualan Chemical Technology Co. Ltd. (China) and Shanghai Lida biotechnology

20、 Co. Ltd. (China), respectively. 2, 2-diphenyl-1-picrylhydrazyl (DPPH) was from SigmaeAldrich Company (St. Louis, USA).2.2. Preparation of filmsThe chitosan solution with concentration of 4 wt% was prepared by dissolving chitosan into 2% (V/V) acetic acid aqueous solution at 60 with stirring of 800

21、rpm. Glycerol, as a plasticizer, was added to the chitosan solution at concentration of 30 wt% of the chitosan. The TP solutions with different concentrations were prepared by mixing TP with distilled water at 60 and stirring with 200 rpm for 10 min. The film solutions were prepared by mixing the ch

22、itosan solution and the TP solutions at weight ratio of 1:1 to fabricate the chitosan films incorporated TP at concentration (weight percentage) of 10%, 20%, 30% and 40% of the chitosan. After stirred with 800 rpm for 60 min at 60 and degassed, desired amount of film solution was distributed into Pe

23、tri dishes for casting and dried at 50 and 30% relative humidity for 24 h. The peeled films were kept in a chamber at room temperature and 75% RH for 48 h prior to experimental use.2.3. Characterization2.3.1. Attenuated total reflectance Fourier transform infrared (ATRFTIR) analysisATR-FTIR spectra

24、of the obtained chitosan/TP films were measured by using a Nexus 670 FTIR Spectrometer with an ATR attachment (Nicolet, USA) to investigate the interactions of chitosan and TP in the films. The measuring probe directly touched the surface of the films. A spectral resolution of 4 cm1 was employed and

25、 64 scans were acquired for each spectrum in the range of 4000 to 1000 cm1.2.3.2. Density, moisture content and opacityFilm density was determined from the specimen weight and volume. The specimen volume was calculated from specimen area and thickness. The specimen thickness was measured by using a

26、hand-held digital micrometer (Mitutoyo Absolute, Tester Sangyo Co. Ltd., Tokyo, Japan) with a precision of 0.001mmat five different positions in each specimen and the average values were taken. Moisture content of the films was determined by measuring weight loss of films upon drying in an oven at 1

27、05 1 C for 24 h. All the tests were conducted in triplicate and the means were reported. The moisture content was calculated according to the following equation:where Mw is the weight of the films conditioned in 75% RH to moisture equilibrium and Md is dry weight of the films.Opacitywas determined a

28、ccording to the method of Park, Je, and Kim (2004) by measuring the film absorbance at 600 nm using a UV spectrophotometer (Ruili Analytical Instrument Company, Beijing, China). The films were cut into a rectangle piece and directly placed in a spectrophotometer test cell. An empty test cell was use

29、d as the reference. The opacity of the films was calculated by the following equation:where O is the opacity, Abs600 is the value of absorbance at 600 nm and d is the film thickness (mm).2.3.3. Color propertiesThe color of the films was evaluated by using a HunterLab ColorFlex (Xinlian Creation Elec

30、tronic Co. Ltd., Shanghai, China). The color values of L* (luminosity), a* (negative-green; positivered) and b* (negative-blue; positive-yellow) were measured. A standard plate CX 2064 was used as standard. The total color difference (DE*) and chroma (C*) were calculated as follows:where DL L* stand

31、ard L* sample, Da a* standard a* sample, Db b* standard b* sample. The color parameter values of the standard plate are L* 94.52, a* 0.86, and b* 0.68. Five measurements were taken on each film, one at the center and four around the perimeter.2.3.4. Water solubility (WS)The WS of the films was defin

32、ed as the percentage of solved specimen dry matter after 24 h of immersion in distilled water and measured according to the method used by Khoshgozaran-Abras, Azizi, Hamidy, and Bagheripoor-Fallah (2012). The chitosan/TP films, previously equilibrated at 75% RH, were cut to 1 cm 4 cm strips, and imm

33、ersed in 50 ml of distilled water and stirred at 100 rpm. After 24 h, the strips were taken out and dried at 1051 for 24 h and the final dry weight (Wf) was measured. The initial dry weight (Wi) was determined by drying the strips in an oven at 105 to constant weight. All the tests were conducted in

34、 triplicate and the means were reported. The water solubility was calculated according to the following equation:2.3.5. Water vapor permeability (WVP)The WVP of the films was determined gravimetrically according to the standard test method GB1037-88 (similar to the relevant ASTM method). Special alu

35、minum cup, with 6.0 cm of internal diameter, 8.3 cm of external diameter (exposed area: 28.26 cm2), and 1.3 cm of depth, was used. The cup was filled with 2 g of fully dried anhydrous CaCl2 in order to provide 0% RH and sealed by the films, then placed into a desiccator at room temperature and 95% R

36、H maintained by KNO3 saturated solution. The cup was weighed periodically (every 2 h for 18 h) using an analytical balance with a precision of 0.1 mg (Mettler-Toledo Instrument (Shanghai) Co. Ltd., China). The water vapor transmission rate (WVTR) of the films was determined from the plot of weight g

37、ained versus time. The slope of the linear portion of this plot represented the steady state amount of water vapor diffusing through the film per unit time. The WVTR was expressed in gram units, per square meter, per day. Steady state over time (slope) yielded a regression coefficient of 0.99 or gre

38、ater. Three specimens per film were tested. The WVP of the films was calculated by multiplying the WVTR by the film thickness and dividing that by the water vapor pressure difference across the films. The WVTR and WVP were determined by using the following equations (Garca, Ribba, Dufresne, Arangure

39、n, & Goyanes, 2009; Srinivasa, Ramesh, & Tharanathan, 2007):where ADPPH is the absorbance value at 517 nm of the methanol solution of DPPH and As is the absorbance value at 517 nm of the DPPH assay solution. Tests were performed six times for each specimen, and the average values were taken.2.4. Sta

40、tistical analysisThe difference between factors and levels was evaluated by the analysis of variance (ANOVA). Duncans multiple range tests were used to compare the means to identify which groups were significantly different from other groups (p 0.05). All data are presented as mean standard deviatio

41、n.3. Results and discussion3.1. Attenuated total reflectance Fourier transform infrared (ATR-FTIR) analysisATR-FTIR spectroscopy was used to observe the interactions between chitosan and TP. When two components are mixed, physical blends versus chemical interactions are reflected by changes in the c

42、haracteristic spectra peaks (Xu, Kim, Hanna, & Nag, 2005). ATR-FTIR spectra of chitosan/TP films were shown in Fig. 1. It can be seen that the peak of NeH bending in chitosan located at 1550 cm1 (Bourtoom & Chinnan, 2008) shifted to 1540 cm1 with the increasing of TP concentration. Another obvious c

43、hangewas the new peak emerged at 1230 cm1 which was ascribable to CO in TP (Evans & Bird, 2008). It was also noted that, with the increasing of TP concentration, the peak located at 1070 cm1 became more flattened and was less discernible and the peak at 1030 cm1 shifted to 1040 cm1. Since the peaks

44、from the symmetric stretch of CeOeC are around 1020e1075 cm1 (Banerjee, Mitra, Singh, Sharma, & Maitra, 2002), the above observations indicated that changes took place in the chain structure of chitosan after TP was added (Pawlak & Mucha, 2003). The results of ATR-FTIR suggested that incorporation o

45、f TP into chitosan caused interactions occurring between chitosan and TP.Fig. 1. ATR-FTIR spectrum of chitosan/TP films.Table 1Density, moisture content and opacity of the chitosan/TP films with different TP concentrations.薄膜密度(g cm-3)水分含量（%）不透明度（A mm-1）0%TP1.1020.07842.710.64e0.4890.045a10%TP1.1320

46、.08936.871.12d1.5870.151b20%TP1.1510.05132.721.74c1.7920.171c30%TP1.1810.09928.400.51b2.2810.081d40%TP1.2310.12025.950.41a2.8980.158eValues are given as mean standard deviation. Different letters in the same column indicate significantly different (p 0.05) when analyzed by Duncans New Multiple Range

47、 Test.3.2. Density, moisture content and opacityThe effects of TP concentration on density, moisture content and opacity of the chitosan/TP films were shown in Table 1. Although the effect of TP incorporation on the density was not significantly (p 0.05), the density of the films still slightly incr

48、eased with the increasing of TP concentration. The moisture content and opacity of the films were significantly (p 0.05) affected by the increasing of TP concentration. The interactions between chitosan and TP is responsible for the fact that the moisture content in the chitosan/TP films decreases w

49、ith the increasing of TP concentration, because the interactions between chitosan and TP could lower the availability of hydroxyl and amino groups, which would, in turn, limit the chitosanewater interactions through hydrogen bonding. According to Eq. (2), the high values of O indicate lower transparency and higher degree of opacity. The control chitosan film (without TP) was more t