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Biological activities of extracts from Tongue fern (Pyrrosia lingua) 원문보기

Journal of applied biological chemistry, v.63 no.3, 2020년, pp.181 - 188  

Akhmadjon, Sultanov (School of Food Science & Biotechnology, Kyungpook National University) ,  Hong, Shin Hyub (School of Food Science & Biotechnology, Kyungpook National University) ,  Lee, Eun-Ho (School of Food Science & Biotechnology, Kyungpook National University) ,  Park, Hye-Jin (School of Food Science & Biotechnology, Kyungpook National University) ,  Cho, Young-Je (School of Food Science & Biotechnology, Kyungpook National University)

Abstract AI-Helper 아이콘AI-Helper

In this study, Tongue fern (Pyrrosia lingua) plants that have been used traditionally as medicines. Their traditional medicinal uses, regions where indigenous people use the plants, parts of the plants used as medicines. This study was designed to assess the antioxidant and inhibition activities of ...

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제안 방법

  • Antioxidant activity in this experiment divided into two solid and phenolic of the extracts was tested DPPH and ABTS, but only in an average concentration of 100 µg/mL was used.
  • The purpose of this study was to evaluate the physiological activities of antioxidant, beauty foods and functional foods using the extracts of P. lingua. According to the above results, the content of total phenolic components and health functional food activities such as antioxidant and gout suppression, and cosmetic activities such as melanogenic improvement and pore reduction effect, etc.

데이터처리

  • 2)The result were expressed as means of triplicates ± standard derivation with different superscript letters are significantly different at p <0.05 by Duncan’s range test (n =3).
  • For checking statistical assay used IBM SPSS Statistics Client Documentation 25.0 for Windows (IBM SPSS Inc., Chicago, IL, USA) and used one-way ANOVA, followed by Duncan’s multiple range tests.

이론/모형

  • The DPPH scavenging activity was measured according to the method of Blois [10]. The initially, using 3 mL of 60 µM DPPH and was added to 1 mL samples as well as mixed by vortex mixer.
  • The PF was measured according to the methods of Andarwulan and Shetty [13]. That is, 1 mL of a solution of 30 mg of β-carotene dissolved in 50 mL of chloroform is placed in a water container for the evaporator, and chloroform is completely distilled in a 40 °C water bath, 20 μL linoleic acid, 184 μL Tween 40 and 50 mL of 0.
  • Tyrosinase inhibition effect was measured according to the method of Hearing and Vincent [20]. The reaction port was 0.
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참고문헌 (36)

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