Laboratory of Pharmaceutical Engineering, Gifu Pharmaceutical University, 5-6-1 Mitahora Higashi, Gifu 502-8585, Japan.
Int J Pharm. 2010 Feb 15;386(1-2):243-8. doi: 10.1016/j.ijpharm.2009.10.044. Epub 2009 Nov 4.
An improved system using both supercritical antisolvent precipitation and rapid expansion from supercritical to aqueous solution (RESAS) was proposed to overcome the problem of low solubility of medicinal substances in scCO(2). When the ethanol solution with IMC was sprayed into the vessel purged with scCO(2), no precipitation of IMC was observed if the CO(2) pressure was more than 15MPa at 40 degrees C. This indicates that very small droplets of the ethanol solution with IMC could disperse in the high pressure CO(2). After expansion into distilled water using an RESAS device, this same solution, in CO(2) at high pressure, produced submicron particles of IMC. For the pharmaceutical application, the IMC suspension was freeze-dried and re-dispersed to the aqueous media. SEM images of freeze-dried sample showed that the suspension was composed of submicron particles with 300-500 nm. Although the average particle size of re-dispersed IMC related significantly to the pressure and temperature in the vessel on scCO(2) processing, the freeze-dried sample of the IMC suspension after the treatment shows good redispersibility as a nanosuspension. This apparatus is found to be a promising way to produce fine crystals of IMC with a high yield.
提出了一种改进的系统,该系统结合了超临界抗溶剂沉淀和从超临界到水溶液的快速膨胀(RESAS),以克服药物在 scCO₂ 中溶解度低的问题。当含有 IMC 的乙醇溶液被喷入用 scCO₂ 吹扫的容器中时,如果在 40℃时 CO₂ 压力超过 15MPa,则不会观察到 IMC 的沉淀。这表明含有 IMC 的乙醇溶液的非常小的液滴可以在高压 CO₂ 中分散。使用 RESAS 装置在蒸馏水中膨胀后,该溶液在高压 CO₂ 中产生 IMC 的亚微米颗粒。对于药物应用,将 IMC 混悬液冷冻干燥并重新分散到水介质中。冷冻干燥样品的 SEM 图像表明,悬浮液由 300-500nm 的亚微米颗粒组成。尽管再分散 IMC 的平均粒径与在 scCO₂ 处理过程中容器中的压力和温度密切相关,但处理后 IMC 混悬液的冷冻干燥样品表现出作为纳米混悬剂的良好再分散性。该设备被发现是一种生产高收率的 IMC 细晶的有前途的方法。