期刊
JOURNAL OF FOOD SCIENCE
卷 85, 期 4, 页码 1060-1069出版社
WILEY
DOI: 10.1111/1750-3841.15084
关键词
fungisome; Inonotus obliquus; L02 cells; oxidative damage
资金
- Tianjin Municipal Science and Technology Foundation [18PTZWHZ00190]
- National Natural Science Foundation of China [31371879]
Inonotus obliquus is a traditional mushroom well known for its therapeutic value. In this study, various solvent fractions of I. obliquus were preliminarily screened for their antioxidant, alpha-amylase and alpha-glucosidase inhibition properties. To improve the drug delivery, the active fraction (ethyl acetate fraction) of I. obliquus was synthesized into fungisome (ethyl acetate phophotidyl choline complex, EAPC) and its physical parameters were assessed using Fourier transform infrared spectroscopy (FTIR), High performance liquid chromatography (HPLC), Scanning electron microscope (SEM), and sigma potential analysis. Then normal human hepatic L02 cells was used to evaluate the cytotoxicity of EAPC. The results showed that EA fraction possesses significant free radical scavenging, alpha-amylase and alpha-glucosidase inhibition properties. FTIR, SEM, and HPLC analysis confirmed the fungisome formation. The particle size of EAPC was 102.80 +/- 0.42 nm and the sigma potential was -54.30 +/- 0.61 mV. The percentage of drug entrapment efficiency was 97.13% and the drug release rates of EAPC in simulated gastric fluid and simulated intestinal fluid were 75.04 +/- 0.29% and 93.03 +/- 0.36%, respectively. EAPC was nontoxic to L02 cells, however it could selectively fight against the H2O2 induced oxidative damage in L02 cells. This is the first study to provide scientific information to utilize the active fraction of I. obliquus as fungisome. Practical Applications Inonotus obliquus (IO) is a traditional medicinal fungus. The extracts of IO have obvious antioxidant and hypoglycemic activities. Ethyl acetate (EA) fraction of IO was encapsulated in liposomes to form EAPC. EAPC has a sustained-release effect. It has nontoxic to L02 cells and could protect L02 cells from oxidative damage caused by hydrogen peroxide. This study could provide new ideas for the treatment of diabetes.
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