Démuth B, Farkas A, Pataki H, Balogh A, Szabó B, Borbás E, Sóti P L, Vigh T, Kiserdei É, Farkas B, Mensch J, Verreck G, Van Assche I, Marosi G, Nagy Z K
Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, 1111 Budapest, Műegyetem rkp. 3., Hungary.
Department of Manufacturing Science and Engineering, Budapest University of Technology and Economics, 1111 Budapest, Műegyetem rkp. 3., Hungary.
Int J Pharm. 2016 Feb 10;498(1-2):234-44. doi: 10.1016/j.ijpharm.2015.12.029. Epub 2015 Dec 15.
In this research the long-term stability (one year) of amorphous solid dispersions (ASDs) prepared by high speed electrospinning was investigated at 25 °C/60% relative humidity (RH) (closed conditions) and 40 °C/75% RH (open conditions). Single needle electrospinning and film casting were applied as reference technologies. Itraconazole (ITR) was used as the model API in 40% concentration and the ASDs consisted of either one of the following polymers as a comparison: polyvinylpyrrolidone-vinyl acetate 6:4 copolymer (no hydrogen bonds between API and polymer) and hydroxypropyl methylcellulose (possible hydrogen bonds between oxo or tertiary nitrogen function of API and hydroxyl moiety of polymer). DSC, XRPD and dissolution characteristics of samples at 0, 3 and 12 months were investigated. In addition, Raman maps of certain electrospun ASDs were assessed to investigate crystallinity. A new chemometric method, based on Multivariate Curve Resolution-Alternating Least Squares algorithm, was developed to calculate the spectrum of amorphous ITR in the matrices and to determine the crystalline/amorphous ratio of aged samples. As it was expected ITR in single needle electrospun SDs was totally amorphous at the beginning, in addition hydroxypropyl methylcellulose could keep ITR in this form at 40 °C/75% RH up to one year due to the hydrogen bonds and high glass transition temperature of the SD. In polyvinylpyrrolidone-vinyl acetate matrix ITR remained amorphous at 25 °C/60% RH throughout one year. Materials prepared by scaled-up, high throughput version of electrospinning, which is compatible with pharmaceutical industry, also gained the same quality. Therefore these ASDs are industrially applicable and with an appropriate downstream process it would be possible to bring them to the market.
在本研究中,对通过高速静电纺丝制备的无定形固体分散体(ASD)在25℃/60%相对湿度(RH)(密闭条件)和40℃/75%RH(开放条件)下的长期稳定性(一年)进行了研究。单针静电纺丝和流延成膜作为参考技术。以40%浓度的伊曲康唑(ITR)作为模型活性药物成分(API),制备的ASD由以下聚合物之一组成,以作比较:聚乙烯吡咯烷酮 - 醋酸乙烯酯6:4共聚物(API与聚合物之间无氢键)和羟丙基甲基纤维素(API中的羰基或叔氮官能团与聚合物的羟基部分之间可能形成氢键)。研究了样品在0、3和12个月时的差示扫描量热法(DSC)、X射线粉末衍射(XRPD)和溶出特性。此外,对某些静电纺丝ASD的拉曼图谱进行了评估以研究结晶度。开发了一种基于多元曲线分辨交替最小二乘法算法的新化学计量学方法,用于计算基质中无定形ITR的光谱,并确定老化样品的结晶/无定形比例。正如预期的那样,单针静电纺丝固体分散体(SD)中的ITR在开始时完全无定形,此外,由于氢键和SD的高玻璃化转变温度,羟丙基甲基纤维素在40℃/75%RH下可使ITR保持这种形式长达一年。在聚乙烯吡咯烷酮 - 醋酸乙烯酯基质中,ITR在25℃/60%RH下一年中均保持无定形。通过与制药行业兼容的放大、高通量版本的静电纺丝制备的材料也具有相同的质量。因此,这些ASD在工业上是适用的,并且通过适当的下游工艺有可能将它们推向市场。