JOURNAL OF LIGHT INDUSTRY

CN 41-1437/TS  ISSN 2096-1553

Volume 37 Issue 6
December 2022
Article Contents
SUN Shidong and ZHAO Wenhong. Oxygen stability and degradation kinetics of amylose-lycopene complexes[J]. Journal of Light Industry, 2022, 37(6): 68-77. doi: 10.12187/2022.06.009
Citation: SUN Shidong and ZHAO Wenhong. Oxygen stability and degradation kinetics of amylose-lycopene complexes[J]. Journal of Light Industry, 2022, 37(6): 68-77. doi: 10.12187/2022.06.009 shu

Oxygen stability and degradation kinetics of amylose-lycopene complexes

  • Received Date: 2022-04-11
  • The structure of amylose-lycopene complexes (ALCs) was characterized, and the changes of lycopene retention and antioxidant activity in ALCs treated with N2 or O2 were studied, and the kinetic model of lycopene degradation was further developed. Results showed that lycopene encapsulated by amylose formed a V-type helix structure, and the molecular chain winding of lycopene and amylose increased the double helix content of ALCs. The content and antioxidant activity of lycopene in ALCs treated with N2 were higher than those treated with O2, and the degradation was slower. After 24 h treatment in N2, the retention rate of lycopene and the clearance rate of DPPH in ALCs were (85.17±0.42)% and (35.74±0.01)%, respectively, which were significantly higher than those in the control group (59.74±0.06)% and (17.20±0.01)% (P < 0.01). After 24 h treatment in O2, the retention rate of lycopene and the clearance rate of DPPH in ALCs were (77.09±0.90)% and (33.24±0.03)%, respectively, which were significantly higher than those of lycopene standard (50.32±0.42)% and (16.32±0.09)% in the control group. Under the condition of N2 and O2 treatment, the degradation of lycopene in ALCs conformed to the second-order kinetic model, the degradation rate constants were 6.0×10-4 μg/(mL·h) and 8.0×10-4 μg/(mL·h), respectively, and the lifetimes of T1/2 was 115.92 h and 86.94 h, respectively, and the T9/10 was 17.57 h and 13.18 h, respectively, which were significantly better than those in the control group. Therefore, the ALCs was effective in enhance lycopene stability, and better maintained the content and antioxidant activity of the lycopene.
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