Biological Science Research, Kao Corporation, 2606 Akabane, Ichikai-machi, Haga-gun, Tochigi 321-3497, Japan.
Biological Science Research, Kao Corporation, 2606 Akabane, Ichikai-machi, Haga-gun, Tochigi 321-3497, Japan.
Int J Pharm. 2019 Mar 10;558:215-224. doi: 10.1016/j.ijpharm.2018.12.092. Epub 2019 Jan 14.
A novel amorphous solid dispersion (ASD) of poorly water-soluble nobiletin (Nob) with highly water-soluble methyl hesperidin (MeHes) was developed. Mixtures of Nob and excipients (MeHes, cellulose derivatives, and synthetic polymers) were processed by hot-melt extrusion (HME). Powder X-ray diffraction analysis proved that most of the HME products were fully amorphized. In dissolution studies, Nob-MeHes ASD showed a prominently higher Nob concentration than other HME products with polymeric excipients. Nob concentration upon dissolution of Nob-MeHes ASD was 400 and 7.5 times higher than that upon dissolution of crystalline Nob and a Nob-MeHes physical mixture, respectively. In addition, Nob-MeHes ASD showed good preservation stability for 6 months under an accelerated condition of 40 °C and 80% relative humidity. Permeation studies using a Caco-2 cell monolayer showed that Nob-MeHes ASD markedly increased the amount of Nob transported. In mice, the plasma Nob concentration and accumulated amount of Nob in various tissues drastically increased after administration of Nob-MeHes ASD. This is the first successful application of MeHes, with a relatively low glass-transition temperature, as an excipient for an ASD formulation prepared by hot-melt extrusion. The drastic improvement in Nob concentration with a small-molecule excipient may be an important finding.
一种新型的难溶性橙皮素(Nob)与高水溶性甲基橙皮苷(MeHes)无定形固体分散体(ASD)被开发出来。将 Nob 与赋形剂(MeHes、纤维素衍生物和合成聚合物)的混合物通过热熔挤出(HME)进行处理。粉末 X 射线衍射分析证明,大多数 HME 产物完全非晶化。在溶解研究中,与含有聚合物赋形剂的其他 HME 产物相比,Nob-MeHes ASD 显示出更高的 Nob 浓度。Nob-MeHes ASD 溶解时的 Nob 浓度分别比结晶型 Nob 和 Nob-MeHes 物理混合物高 400 倍和 7.5 倍。此外,在 40°C 和 80%相对湿度的加速条件下,Nob-MeHes ASD 经过 6 个月仍具有良好的保存稳定性。使用 Caco-2 细胞单层的渗透研究表明,Nob-MeHes ASD 显著增加了 Nob 的转运量。在小鼠中,给予 Nob-MeHes ASD 后,血浆中 Nob 浓度和各种组织中 Nob 的累积量急剧增加。这是首次成功应用玻璃化转变温度相对较低的 MeHes 作为热熔挤出法制备的 ASD 制剂的赋形剂。用小分子赋形剂大幅提高 Nob 浓度可能是一个重要发现。