Department of Pharmacy, Faculty of Health, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.
Sirius Analytical Instruments Ltd., Station Rd, Forest Row RH18 5DW, United Kingdom.
Eur J Pharm Biopharm. 2018 Jan;122:62-69. doi: 10.1016/j.ejpb.2017.10.001. Epub 2017 Oct 3.
In situ amorphization is an approach that enables a phase transition of a crystalline drug to its amorphous form immediately prior to administration. In this study, three different polyvinylpyrrolidones (PVP K12, K17 and K25) were selected to investigate the influence of the molecular weight of the polymer on the degree of amorphization of the model drug indomethacin (IND) upon microwaving. Powder mixtures of crystalline IND and the respective PVP were compacted at 1:2 (w/w) IND:PVP ratios, stored at 54% RH and subsequently microwaved with a total energy input of 90 or 180kJ. After storage, all compacts had a similar moisture content (∼10% (w/w)). Upon microwaving with an energy input of 180kJ, 58±4% of IND in IND:PVP K12 compacts was amorphized, whereas 31±8% of IND was amorphized by an energy input of 90kJ. The drug stayed fully crystalline in all IND:PVP K17 and IND:PVP K25 compacts. After plasticization by moisture, PVP K12 reached a T below ambient temperature (16±2°C) indicating that the T of the plasticized polymer is a key factor for the success of in situ amorphization. DSC analysis showed that the amorphized drug was part of a ternary glass solution consisting of IND, PVP K12 and water. In dissolution tests, IND:PVP K12 compacts showed a delayed initial drug release due to a lack of compact disintegration, but reached a higher total drug release eventually. In summary, this study showed that the microwave assisted in situ amorphization was highly dependent on the T of the plasticized polymer.
原位非晶化是一种方法,可使药物的结晶相在给药前立即转变为无定形相。在这项研究中,选择了三种不同的聚乙烯吡咯烷酮(PVP K12、K17 和 K25),以研究聚合物分子量对模型药物吲哚美辛(IND)在微波作用下非晶化程度的影响。将结晶 IND 和相应 PVP 的粉末混合物以 1:2(w/w)的 IND:PVP 比例压实,在 54%RH 下储存,然后用 90 或 180kJ 的总能量输入进行微波处理。储存后,所有压块的水分含量相似(约 10%(w/w))。用 180kJ 的能量输入微波处理时,IND:PVP K12 压块中 58±4%的 IND 被非晶化,而用 90kJ 的能量输入时,31±8%的 IND 被非晶化。在所有 IND:PVP K17 和 IND:PVP K25 压块中,药物均保持完全结晶。在被水分塑化后,PVP K12 的 T 低于环境温度(16±2°C),这表明塑化聚合物的 T 是原位非晶化成功的关键因素。DSC 分析表明,无定形药物是由 IND、PVP K12 和水组成的三元玻璃溶液的一部分。在溶解试验中,由于缺乏压块崩解,IND:PVP K12 压块的初始药物释放延迟,但最终达到更高的总药物释放。总之,这项研究表明,微波辅助原位非晶化高度依赖于塑化聚合物的 T。