Preparation, physicochernical characterization, and antioxidant effects of quercetin nanoparticles

被引:286
作者
Wu, Tzu-Hui [2 ,3 ]
Yen, Feng-Lin [2 ]
Lin, Liang-Tzung [4 ]
Tsai, Tong-Rong [1 ]
Lin, Chun-Ching [1 ]
Cham, Thau-Ming [1 ]
机构
[1] Kaohsiung Univ, Coll Pharm, Fac Pharm, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ, Coll Pharm, Grad Sch Pharmaceut Sci, Kaohsiung, Taiwan
[3] Hlth Bur Kaohsiung County Govt, Kaohsiung, Taiwan
[4] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 3J5, Canada
关键词
quercetin; nanoparticles; H-1 nuclear magnetic resonance; free radical-scavenging activity; anti-lipid peroxidation;
D O I
10.1016/j.ijpharm.2007.06.036
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to develop quercetin-loaded nanoparticles (QUEN) by a nanoprecipitation technique with Eudragit (R) E (EE) and polyvinyl alcohol (PVA) as carriers, and to evaluate the antioxidant effects of quercetin (QU) and of its nanoparticles. The novel QUEN systems were characterized by particle size and morphology, yield and encapsulation efficiency, differential scanning calorimetry (DSC), powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), H-1 nuclear magnetic resonance (H-1 NMR), and dissolution study. It was observed that the weight ratio of QU:EE:PVA at 1: 10: 10 carried a particle size of <85 nm, a particle distribution with polydispersity index <0.3, and its yield and encapsulation efficiency were over 99%. The results from XRD and DSC of the QUEN showed that the crystal of the drug might be converted to an amorphous state. The FT-IR and H-1 NMR demonstrated that QU formed intermolecular hydrogen bonding with carriers. The release of the drug from the QUEN was 74-fold higher compared with the pure drug. In addition, the antioxidant activity of the QUEN was more effective than pure QU on DPPH scavenging, anti-superoxide formation, superoxide anion scavenging, and anti-lipid peroxidation. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 168
页数:9
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