Ahmed Tarek A
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia; Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.
Int J Nanomedicine. 2016 Feb 2;11:515-27. doi: 10.2147/IJN.S98080. eCollection 2016.
In this study, optimized freeze-dried finasteride nanoparticles (NPs) were prepared from drug nanosuspension formulation that was developed using the bottom-up technique. The effects of four formulation and processing variables that affect the particle size and solubility enhancement of the NPs were explored using the response surface optimization design. The optimized formulation was morphologically characterized using transmission electron microscopy (TEM). Physicochemical interaction among the studied components was investigated. Crystalline change was investigated using X-ray powder diffraction (XRPD). Crystal growth of the freeze-dried NPs was compared to the corresponding aqueous drug nanosuspension. Freeze-dried NPs formulation was subsequently loaded into hard gelatin capsules that were examined for in vitro dissolution and pharmacokinetic behavior. Results revealed that in most of the studied variables, some of the quadratic and interaction effects had a significant effect on the studied responses. TEM image illustrated homogeneity and shape of the prepared NPs. No interaction among components was noticed. XRPD confirmed crystalline state change in the optimized NPs. An enhancement in the dissolution rate of more than 2.5 times from capsules filled with optimum drug NPs, when compared to capsules filled with pure drug, was obtained. Crystal growth, due to Ostwald ripening phenomenon and positive Gibbs free energy, was reduced following lyophilization of the nanosuspension formulation. Pharmacokinetic parameters from drug NPs were superior to that of pure drug and drug microparticles. In conclusion, freeze-dried NPs based on drug nanosuspension formulation is a successful technique in enhancing stability, solubility, and in vitro dissolution of poorly water-soluble drugs with possible impact on the drug bioavailability.
在本研究中,采用自下而上技术开发的药物纳米混悬液制剂制备了优化的冻干非那雄胺纳米颗粒(NPs)。使用响应面优化设计探索了影响NPs粒径和溶解度增强的四个制剂和工艺变量的作用。使用透射电子显微镜(TEM)对优化后的制剂进行形态表征。研究了所研究成分之间的物理化学相互作用。使用X射线粉末衍射(XRPD)研究结晶变化。将冻干NPs的晶体生长与相应的水性药物纳米混悬液进行比较。随后将冻干NPs制剂装入硬明胶胶囊中,对其进行体外溶出度和药代动力学行为研究。结果表明,在大多数研究变量中,一些二次效应和相互作用效应对所研究的响应有显著影响。TEM图像显示了所制备NPs的均匀性和形状。未观察到成分之间的相互作用。XRPD证实了优化后NPs的结晶状态变化。与填充纯药物的胶囊相比,填充最佳药物NPs的胶囊溶出速率提高了2.5倍以上。由于奥斯特瓦尔德熟化现象和正吉布斯自由能,纳米混悬液制剂冻干后晶体生长减少。药物NPs的药代动力学参数优于纯药物和药物微粒。总之,基于药物纳米混悬液制剂的冻干NPs是一种成功的技术,可提高难溶性药物的稳定性、溶解度和体外溶出度,并可能影响药物的生物利用度。