Sonoda Ryoichi, Hara Yuko, Iwasaki Tomohiro, Watano Satoru
Drug Formulation Department, Central Research Laboratories, Kaken Pharmaceutical Co., Ltd., Fujieda, Shizuoka 426-8646, Japan.
Chem Pharm Bull (Tokyo). 2009 Oct;57(10):1040-4. doi: 10.1248/cpb.57.1040.
The dissolution property of the poorly water-soluble drug, flurbiprofen (FP) was improved by a novel supercritical freeze granulation using supercritical carbon dioxide. Supercritical freeze granulation was defined as a production method of the granulated substances by using the dry ice to generate intentionally for the rapid atomization of the supercritical carbon dioxide to the atmospheric pressure. This process utilized a rapid expansion of supercritical solutions (RESS) process with the mixture of the drug and lactose. In the supercritical freeze granulation, needle-like FP fine particles were obtained which adhered to the surface of lactose particles, which did not dissolve in supercritical carbon dioxide. The number of FP particles that adhered to the surface of particles decreased with an increase in the ratio of lactose added, leading to markedly improve the dissolution rate. This improvement was caused not only by the increase in the specific surface area but also the improvement of the dispersibility of FP in water. It is thus concluded that the supercritical freeze granulation is a useful technique to improve the dissolution property of the poorly water-soluble flurbiprofen.
采用新型超临界冷冻造粒法,利用超临界二氧化碳改善了难溶性药物氟比洛芬(FP)的溶出性能。超临界冷冻造粒被定义为一种通过使用干冰使超临界二氧化碳快速雾化至常压来制备颗粒物质的生产方法。该过程利用了超临界溶液快速膨胀(RESS)工艺以及药物与乳糖的混合物。在超临界冷冻造粒过程中,获得了附着在乳糖颗粒表面的针状FP细颗粒,乳糖颗粒不溶于超临界二氧化碳。随着乳糖添加比例的增加,附着在颗粒表面的FP颗粒数量减少,从而显著提高了溶出速率。这种改善不仅是由于比表面积的增加,还由于FP在水中分散性的提高。因此得出结论,超临界冷冻造粒是改善难溶性氟比洛芬溶出性能的一种有用技术。