State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences (ICMS) , University of Macau , Macau , China.
Aston Pharmacy School, School of Life and Health Sciences , Aston University , Birmingham B4 7ET , United Kingdom.
Mol Pharm. 2018 Apr 2;15(4):1664-1673. doi: 10.1021/acs.molpharmaceut.8b00056. Epub 2018 Mar 15.
Cyclodextrin (CD) complexation is widely used for the solubilization of poorly soluble drugs in the pharmaceutical industry. Current research was to develop a highly soluble lutein-cyclodextrin multiple-component delivery system (lutein-CD-MCDS) by combined modeling and experimental approaches. Both phase solubility diagram and molecular dynamics (MD) simulation results revealed that the interactions between lutein and CDs were very weak, which confirmed the insignificant solubility improvement of lutein-CD binary system. On the basis of theoretical calculation and preliminary CD studies, lutein-CD-MCDS was developed with over 400-fold solubility improvement after formulation screening. MD simulation indicated that the auxiliary polymers of TWEEN 80 and poloxamer 188 in the lutein-CD-MCDS introduced bridged interaction between lutein and γ-CD to increase the solubility, dissolution rate, and stability of the complex. The lutein-CD-MCDS was characterized by in vitro dissolution test, differential scanning colorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and powder X-ray diffraction (PXRD). Moreover, lutein-CD-MCDS had significantly higher uptake in Caco-2 cells than free lutein. The relative bioavailability of the lutein-CD-MCDS increased to 6.6-fold compared to pure lutein, and to 1.2-fold compared with commercial lutein soft capsules. In conclusion, the highly soluble lutein-CD-MCDS with significant improvement in both the solubility and bioavailability was developed and characterized by combined modeling and experimental approaches. Our research indicates that computer-aided formulation design is a promising approach for future formulation development.
环糊精(CD)络合广泛用于医药行业中提高难溶性药物的溶解度。本研究旨在通过组合建模和实验方法开发高溶解度叶黄素-Cd 多组分传递系统(叶黄素-Cd-MCDS)。相溶解度图和分子动力学(MD)模拟结果表明,叶黄素与 CDs 之间的相互作用非常弱,这证实了叶黄素-Cd 二元体系的溶解度提高并不显著。基于理论计算和初步的 CD 研究,通过配方筛选,叶黄素-Cd-MCDS 的溶解度提高了 400 多倍。MD 模拟表明,TWEEN 80 和泊洛沙姆 188 等辅助聚合物在叶黄素-Cd-MCDS 中引入了叶黄素与 γ-CD 之间的桥接相互作用,从而提高了复合物的溶解度、溶解速率和稳定性。通过体外溶出度试验、差示扫描量热法(DSC)、傅里叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)和粉末 X 射线衍射(PXRD)对叶黄素-Cd-MCDS 进行了表征。此外,与游离叶黄素相比,叶黄素-Cd-MCDS 在 Caco-2 细胞中的摄取量显著增加。与纯叶黄素相比,叶黄素-Cd-MCDS 的相对生物利用度提高了 6.6 倍,与市售叶黄素软胶囊相比提高了 1.2 倍。综上所述,采用组合建模和实验方法开发并表征了具有高溶解度和显著提高溶解度和生物利用度的叶黄素-Cd-MCDS。我们的研究表明,计算机辅助配方设计是未来制剂开发的一种有前途的方法。