Comparative Study on Inhibition of Pancreatic Cancer Cells by Resveratrol Gold Nanoparticles and a Resveratrol Nanoemulsion Prepared from Grape Skin

被引:22
作者
Inbaraj, Baskaran Stephen [1 ]
Hua, Leng-Huei [1 ]
Chen, Bing-Huei [1 ,2 ]
机构
[1] Fu Jen Catholic Univ, Dept Food Sci, New Taipei 24205, Taiwan
[2] China Med Univ, Dept Nutr, Taichung 40401, Taiwan
关键词
grape skin; resveratrol-gold nanoparticle; resveratrol nanoemulsion; pancreatic cancer cells BxPC-3; western blotting; ANTIOXIDANT ACTIVITY; IN-VITRO; GLUCURONIDATION; BIOAVAILABILITY; DOXORUBICIN; BREAST; GROWTH; SIZE;
D O I
10.3390/pharmaceutics13111871
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Resveratrol, a phenolic compound possessing vital biological activities such as anti-cancer, is present abundantly in grape skin, a waste produced during the processing of grape juice. The objectives of this study were to prepare resveratrol-gold nanoparticles and a resveratrol nanoemulsion from grape skin and study their inhibition effects on pancreatic cancer cells BxPC-3. The spherical-shaped citrate gold nanoparticles (GNPs) and resveratrol-gold nanoparticles (R-GNPs) were, respectively, prepared with a surface plasmon resonance peak at 528 and 538 nm, mean particle size of 20.8 and 11.9 nm, and zeta-potential at -32.7 and -66.7 mV, by controlling an appropriate concentration of citrate/resveratrol and gold chloride as well as stirring time and temperature. The resveratrol nanoemulsion, composed of soybean oil, Tween 80, and sucrose fatty acid ester in glycerol and water, possessed a high storage stability with a mean particle size of 14.1 nm, zeta-potential of -49.7 mV, and encapsulation efficiency of 95.5%. An antiproliferation study revealed that both R-GNPs and resveratrol nanoemulsion could effectively inhibit the growth of pancreatic cancer cells BxPC-3, with the latter showing a higher inhibition effect. Western blot analysis implied that both can down-regulate expressions of cyclin A, cyclin B, CDK1, and CDK2 and up-regulate expressions of p53 and p21, accompanied by enhancing cytochrome C expression, decreasing BcL-2 expression, increasing Bax expression, and leading to the elevation of caspase-8, caspase-9, and caspase-3 activities for cell apoptosis execution. Future research is needed to study the inhibition of pancreatic tumors in vivo by R-GNPs and resveratrol nanoemulsions.
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页数:19
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