4.7 Article

Synthesis of Short-Chain-Fatty-Acid Resveratrol Esters and Their Antioxidant Properties

期刊

ANTIOXIDANTS
卷 10, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/antiox10030420

关键词

resveratrol esters; resveratrol; short-chain fatty acids; Steglich esterification; antioxidation

资金

  1. Ministry of Science and Technology, Republic of China [108-2221-E-992-046, 109-2221-E-992-051]
  2. Kaohsiung Chang Gung Memorial Hospital, Taiwan [CORPG8L0301]
  3. USDA-ARS [SCA 5860667081]

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In this study, short chain fatty acid esters of resveratrol were successfully prepared by Steglich reactions with acetic, propionic, and butyric acids. The esterified products showed successful esterification and exhibited excellent biological activity and antioxidant properties.
To expand the applications and enhance the stability and bioactivity of resveratrol (RE), and to simultaneously include the potential health benefits of short chain fatty acids (SCFA) esters of RE were prepared by Steglich reactions with acetic, propionic, and butyric acids, respectively. RE and the esterified RE-SCFA products (including RAE, RPE, and RBE) were analyzed using nuclear magnetic resonance (NMR), Fourier-transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), differential thermal analysis (DTA), and liquid chromatography-mass spectrometry (LC-MS). The FTIR and C-13 NMR spectra of the esterified products included ester-characteristic peaks at 1751 cm(-1) and 171 ppm, respectively. Moreover, the peaks in the range of 1700 to 1600 cm(-1) in the FTIR spectra of the esterified products indicated that the esterification of RE-SCFA was successful. The TGA results revealed that the RE-SCFA esters decomposed at lower temperatures than RE. The peaks in the LC-MS profiles of the esterified products indicated the formation of mono- and diesters, and the calculated monoester synthesis rates ranged between 45.81 and 49.64%. The RE esters inhibited the Cu2+-induced low-density lipoprotein oxidation reaction, exhibited antioxidant activity in bulk oil, and effectively inhibited the hydroxyl radical-induced DNA scission. Moreover, the RE-SCFA esters had better hydrogen peroxide scavenging activity than RE. Our results are the first in the literature to successfully including short chain fatty acids in the esters of resveratrol, and the products could be used as a functional food ingredient in processed foods or can be used as dietary supplements to promote health.

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