Enhanced water solubility, antioxidant activity, and oral absorption of hesperetin by D--tocopheryl polyethylene glycol 1000 succinate and phosphatidylcholine

被引:19
作者
Gu, Su-fang [1 ,2 ]
Wang, Li-ying [1 ,2 ]
Tian, Ying-jie [3 ]
Zhou, Zhu-xian [1 ,2 ]
Tang, Jian-bin [1 ,2 ]
Liu, Xiang-rui [1 ,2 ]
Jiang, Hai-ping [4 ]
Shen, You-qing [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Minist Educ, Key Lab Biomass Chem Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Coll Chem & Biol Engn, Ctr Bionanoengn, Hangzhou 310027, Zhejiang, Peoples R China
[3] Hangzhou Ubao Healthcare Technol Co Ltd, Hangzhou 310012, Zhejiang, Peoples R China
[4] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Med Oncol, Hangzhou 310006, Zhejiang, Peoples R China
来源
JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B | 2019年 / 20卷 / 03期
基金
中国国家自然科学基金;
关键词
Hesperetin; D--Tocopheryl polyethylene glycol 1000 succinate (TPGS); Phosphatidylcholine; Antioxidant activity; Oral absorption; CITRUS FLAVONOIDS HESPERIDIN; VITAMIN-E-TPGS; PHOSPHOLIPID COMPLEX; IN-VITRO; PHARMACOKINETICS; BIOAVAILABILITY; NANOPARTICLES; METABOLISM; DOCETAXEL; EFFICACY;
D O I
10.1631/jzus.B1800346
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hesperetin, an abundant bioactive component of citrus fruits, is poorly water-soluble, resulting in low oral bioavailability. We developed new formulations to improve the water solubility, antioxidant activity, and oral absorption of hesperetin. Two nano-based formulations were developed, namely hesperetin-TPGS (D--tocopheryl polyethylene glycol 1000 succinate) micelles and hesperetin-phosphatidylcholine (PC) complexes. These two formulations were prepared by a simple technique called solvent dispersion, using US Food and Drug Administration (FDA)-approved excipients for drugs. Differential scanning calorimetry (DSC) and dynamic light scattering (DLS) were used to characterize the formulations' physical properties. Cytotoxicity analysis, cellular antioxidant activity assay, and a pharmacokinetic study were performed to evaluate the biological properties of these two formulations. The final weight ratios of both hesperetin to TPGS and hesperetin to PC were 1:12 based on their water solubility, which increased to 21.5- and 20.7-fold, respectively. The hesperetin-TPGS micelles had a small particle size of 26.19 nm, whereas the hesperetin-PC complexes exhibited a larger particle size of 219.15 nm. In addition, the cellular antioxidant activity assay indicated that both hesperetin-TPGS micelles and hesperetin-PC complexes increased the antioxidant activity of hesperetin to 4.2- and 3.9-fold, respectively. Importantly, the in vivo oral absorption study on rats indicated that the micelles and complexes significantly increased the peak plasma concentration (C-max) from 2.64 g/mL to 20.67 and 33.09 g/mL and also increased the area under the concentration-time curve of hesperetin after oral administration to 16.2- and 18.0-fold, respectively. The micelles and complexes increased the solubility and remarkably improved the in vitro antioxidant activity and in vivo oral absorption of hesperetin, indicating these formulations' potential applications in drugs and healthcare products.
引用
收藏
页码:273 / 281
页数:9
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