Self-Nanoemulsifying Drug Delivery System for Resveratrol: Enhanced Oral Bioavailability and Reduced Physical Fatigue in Rats

被引:54
|
作者
Yen, Ching-Chi [1 ]
Chang, Chih-Wei [1 ]
Hsu, Mei-Chich [2 ,3 ]
Wu, Yu-Tse [1 ,3 ]
机构
[1] Kaohsiung Med Univ, Sch Pharm, Coll Pharm, 100 Shih Chuan 1st Rd, Kaohsiung 80708, Taiwan
[2] Kaohsiung Med Univ, Dept Sports Med, 100 Shih Chuan 1st Rd, Kaohsiung 80708, Taiwan
[3] Kaohsiung Med Univ Hosp, Dept Med Res, Coll Med, 100 Tzyou 1st Rd, Kaohsiung 80708, Taiwan
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2017年 / 18卷 / 09期
关键词
resveratrol; self-nanoemulsifying drug delivery system; anti-fatigue; SOLID LIPID NANOPARTICLES; IN-VITRO; EXERCISE PERFORMANCE; STRENUOUS EXERCISE; TRANS-RESVERATROL; LIPOPHILIC DRUGS; ABSORPTION; MUSCLE; SUPPLEMENTATION; SOLUBILITY;
D O I
10.3390/ijms18091853
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
Resveratrol (RES), a natural polyphenolic compound, exerts anti-fatigue activity, but its administration is complicated by its low water solubility. To improve RES bioavailability, this study developed a self-nanoemulsifying drug delivery system (SNEDDS) for RES and evaluated its anti-fatigue activity and rat exercise performance by measuring fatigue-related parameters, namely lactate, ammonia, plasma creatinine phosphokinase, and glucose levels and the swimming time to exhaustion. Through solubility and emulsification testing, the optimized SNEDDS composed of Capryol 90, Cremophor EL, and Tween 20 was developed; the average particle size in this formulation, which had favorable self-emulsification ability, was approximately 41.3 +/- 4.1 nm. Pharmacokinetic studies revealed that the oral bioavailability of the optimized RES-SNEDDS increased by 3.2-fold compared with that of the unformulated RES-solution. Pretreatment using the RES-SNEDDS before exercise accelerated the recovery of lactate after exercise; compared with the vehicle group, the plasma ammonia level in the RES-SNEDDS group significantly decreased by 65.4%, whereas the glucose level significantly increased by approximately 1.8-fold. Moreover, the swimming time to exhaustion increased by 2.1- and 1.8-fold, respectively, compared with the vehicle and RES-solution pretreatment groups. Therefore, the developed RES-SNEDDS not only enhances the oral bioavailability of RES but may also exert anti-fatigue pharmacological effect.
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页数:14
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