Key Laboratory of Biomass Chemical Engineering of Ministry of Education and Center for Bionanoengineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China.
Hangzhou Ubao Healthcare Technology Co., Ltd., Hangzhou 310012, China.
J Zhejiang Univ Sci B. 2019;20(3):273-281. doi: 10.1631/jzus.B1800346.
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-α-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) from 2.64 μg/mL to 20.67 and 33.09 μg/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.
橙皮素是柑橘类水果中丰富的生物活性成分,但水溶性差,导致口服生物利用度低。我们开发了新的制剂来提高橙皮素的水溶性、抗氧化活性和口服吸收。开发了两种基于纳米的制剂,即橙皮素-TPGS(D-α-生育酚聚乙二醇 1000 琥珀酸酯)胶束和橙皮素-磷脂酰胆碱(PC)复合物。这两种制剂是通过一种简单的技术制备的,称为溶剂分散,使用美国食品和药物管理局(FDA)批准的药物辅料。差示扫描量热法(DSC)和动态光散射(DLS)用于表征制剂的物理性质。细胞毒性分析、细胞抗氧化活性测定和药代动力学研究用于评估这两种制剂的生物学性质。基于其水溶性,两种橙皮素与 TPGS 和橙皮素与 PC 的最终重量比均为 1:12,分别提高了 21.5 倍和 20.7 倍。橙皮素-TPGS 胶束的粒径较小,为 26.19nm,而橙皮素-PC 复合物的粒径较大,为 219.15nm。此外,细胞抗氧化活性测定表明,橙皮素-TPGS 胶束和橙皮素-PC 复合物均使橙皮素的抗氧化活性分别提高到 4.2 倍和 3.9 倍。重要的是,大鼠体内口服吸收研究表明,胶束和复合物分别使橙皮素的峰血浆浓度(C)从 2.64μg/mL 显著增加到 20.67μg/mL 和 33.09μg/mL,并且使橙皮素口服后的浓度-时间曲线下面积分别增加到 16.2 倍和 18.0 倍。胶束和复合物提高了橙皮素的溶解度,并显著提高了其体外抗氧化活性和体内口服吸收,表明这些制剂在药物和保健品中有潜在的应用。