Cinnamon essential oil liposomes modified by sodium alginate‐chitosan: application in chilled pork preservation

Summary In this study, cinnamon essential oil liposomes (CEO‐Lip), chitosan (CH) modified CEO‐Lip (CH‐CEO‐Lip) and sodium alginate (SA) and CH modified CEO‐Lip (SA‐CH‐CEO‐Lip) were prepared based on layer‐by‐layer electrostatic self‐assembly deposition technique and their preservative effects on fre...

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Veröffentlicht in:International journal of food science & technology 2023-02, Vol.58 (2), p.939-953
Hauptverfasser: Tu, Qian, Li, Shanshan, Zeng, Zhen, Liu, Yuntao, Wang, Caixia, Chen, Saiyan, Hu, Bin, Li, Cheng
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container_title International journal of food science & technology
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creator Tu, Qian
Li, Shanshan
Zeng, Zhen
Liu, Yuntao
Wang, Caixia
Chen, Saiyan
Hu, Bin
Li, Cheng
description Summary In this study, cinnamon essential oil liposomes (CEO‐Lip), chitosan (CH) modified CEO‐Lip (CH‐CEO‐Lip) and sodium alginate (SA) and CH modified CEO‐Lip (SA‐CH‐CEO‐Lip) were prepared based on layer‐by‐layer electrostatic self‐assembly deposition technique and their preservative effects on fresh pork were investigated. The average particle size of SA‐CH‐CEO‐Lip was 178.73 nm with polymer dispersity index (PDI) of 0.380, zeta potential of −23.83 mV. Results showed that the formation of SA‐CH‐CEO‐Lip was efficient (encapsulation efficiency 89.5%). Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) confirmed that SA‐CH‐CEO‐Lip was prepared successfully. The in vitro cumulative release study during 72 h revealed that SA‐CH‐CEO‐Lip (71.42%) showed better sustained release capability than CEO‐Lip (81.24%). The pork assessment test showed that SA‐CH‐CEO‐Lip could effectively inhibit the increase in pH, total volatile basic nitrogen (TVB‐N) and thiobarbituric acid reactants (TBARS) of pork compared with CEO‐Lip group (P 
doi_str_mv 10.1111/ijfs.16140
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The average particle size of SA‐CH‐CEO‐Lip was 178.73 nm with polymer dispersity index (PDI) of 0.380, zeta potential of −23.83 mV. Results showed that the formation of SA‐CH‐CEO‐Lip was efficient (encapsulation efficiency 89.5%). Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) confirmed that SA‐CH‐CEO‐Lip was prepared successfully. The in vitro cumulative release study during 72 h revealed that SA‐CH‐CEO‐Lip (71.42%) showed better sustained release capability than CEO‐Lip (81.24%). The pork assessment test showed that SA‐CH‐CEO‐Lip could effectively inhibit the increase in pH, total volatile basic nitrogen (TVB‐N) and thiobarbituric acid reactants (TBARS) of pork compared with CEO‐Lip group (P &lt; 0.05). The total number of colonies (TBC) showed that the storage life of SA‐CH‐CEO‐Lip group could be extended to 12 days, which was significantly different from that of control group (6 days) (P &lt; 0.05). In addition, SA‐CH‐CEO‐Lip also effectively maintained the good sensory quality of pork. In conclusion, SA‐CH‐CEO‐Lip showed good antiseptic effects on chilled pork preservation. Cinnamon essential oil liposomes (CEO‐Lip) were prepared with thin‐film dispersion method. Since liposome has negatively charged surfaces, while there is a positively charged amino group in chitosan molecular, liposome suspension will electrostatically bind to the particle surface of chitosan. Moreover, the free carboxyl group in sodium alginate solution is negatively charged, and can self‐assemble to the surface of liposome‐chitosan particles. Therefore, by using self‐assembly deposition technology, the liposome surface can be modified to be more robust. 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The average particle size of SA‐CH‐CEO‐Lip was 178.73 nm with polymer dispersity index (PDI) of 0.380, zeta potential of −23.83 mV. Results showed that the formation of SA‐CH‐CEO‐Lip was efficient (encapsulation efficiency 89.5%). Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) confirmed that SA‐CH‐CEO‐Lip was prepared successfully. The in vitro cumulative release study during 72 h revealed that SA‐CH‐CEO‐Lip (71.42%) showed better sustained release capability than CEO‐Lip (81.24%). The pork assessment test showed that SA‐CH‐CEO‐Lip could effectively inhibit the increase in pH, total volatile basic nitrogen (TVB‐N) and thiobarbituric acid reactants (TBARS) of pork compared with CEO‐Lip group (P &lt; 0.05). The total number of colonies (TBC) showed that the storage life of SA‐CH‐CEO‐Lip group could be extended to 12 days, which was significantly different from that of control group (6 days) (P &lt; 0.05). 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technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tu, Qian</au><au>Li, Shanshan</au><au>Zeng, Zhen</au><au>Liu, Yuntao</au><au>Wang, Caixia</au><au>Chen, Saiyan</au><au>Hu, Bin</au><au>Li, Cheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cinnamon essential oil liposomes modified by sodium alginate‐chitosan: application in chilled pork preservation</atitle><jtitle>International journal of food science &amp; technology</jtitle><date>2023-02</date><risdate>2023</risdate><volume>58</volume><issue>2</issue><spage>939</spage><epage>953</epage><pages>939-953</pages><issn>0950-5423</issn><eissn>1365-2621</eissn><abstract>Summary In this study, cinnamon essential oil liposomes (CEO‐Lip), chitosan (CH) modified CEO‐Lip (CH‐CEO‐Lip) and sodium alginate (SA) and CH modified CEO‐Lip (SA‐CH‐CEO‐Lip) were prepared based on layer‐by‐layer electrostatic self‐assembly deposition technique and their preservative effects on fresh pork were investigated. The average particle size of SA‐CH‐CEO‐Lip was 178.73 nm with polymer dispersity index (PDI) of 0.380, zeta potential of −23.83 mV. Results showed that the formation of SA‐CH‐CEO‐Lip was efficient (encapsulation efficiency 89.5%). Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) confirmed that SA‐CH‐CEO‐Lip was prepared successfully. The in vitro cumulative release study during 72 h revealed that SA‐CH‐CEO‐Lip (71.42%) showed better sustained release capability than CEO‐Lip (81.24%). The pork assessment test showed that SA‐CH‐CEO‐Lip could effectively inhibit the increase in pH, total volatile basic nitrogen (TVB‐N) and thiobarbituric acid reactants (TBARS) of pork compared with CEO‐Lip group (P &lt; 0.05). The total number of colonies (TBC) showed that the storage life of SA‐CH‐CEO‐Lip group could be extended to 12 days, which was significantly different from that of control group (6 days) (P &lt; 0.05). In addition, SA‐CH‐CEO‐Lip also effectively maintained the good sensory quality of pork. In conclusion, SA‐CH‐CEO‐Lip showed good antiseptic effects on chilled pork preservation. Cinnamon essential oil liposomes (CEO‐Lip) were prepared with thin‐film dispersion method. Since liposome has negatively charged surfaces, while there is a positively charged amino group in chitosan molecular, liposome suspension will electrostatically bind to the particle surface of chitosan. Moreover, the free carboxyl group in sodium alginate solution is negatively charged, and can self‐assemble to the surface of liposome‐chitosan particles. Therefore, by using self‐assembly deposition technology, the liposome surface can be modified to be more robust. Finally, polymer‐modified liposomes were applied to chilled pork.</abstract><cop>Oxford</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/ijfs.16140</doi><tpages>953</tpages><orcidid>https://orcid.org/0000-0003-1331-1679</orcidid></addata></record>
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source Oxford Journals Open Access Collection; Wiley Online Library All Journals
subjects Alginic acid
Calorimetry
Chilled pork
Chitosan
cinnamon essential oil
Controlled release
Differential scanning calorimetry
Essential oils
Fourier transforms
Infrared spectroscopy
Liposomes
Oils & fats
Polymers
Pork
Preservation
Preservatives
Sensory properties
Sodium
Sodium alginate
Storage life
Sustained release
Thiobarbituric acid
Zeta potential
title Cinnamon essential oil liposomes modified by sodium alginate‐chitosan: application in chilled pork preservation
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