Augsten Christian, Kiselev Mikhail A, Gehrke Rainer, Hause Gerd, Mäder Karsten
Martin-Luther-University of Halle-Wittenberg, Institute of Pharmacy, 06120 Halle, Germany.
J Pharm Biomed Anal. 2008 May 12;47(1):95-102. doi: 10.1016/j.jpba.2007.12.031. Epub 2007 Dec 26.
Poly(d,l-lactide-co-glycolide) nanosupensions as intravenous nanosphere systems were produced by solvent deposition in aqueous Poloxamer 188 solutions. Light scattering techniques were applied to these colloidal systems to characterize particle sizes. Regularly shaped spherical particles were received as proved by freeze fracture replica and small-angle X-ray scattering (SAXS). SAXS was performed using intensive synchrotron radiation. Particle sizes were calculated from the small-angle part of scattering curve that were in good agreement with z-average values received from photon correlation spectroscopy (PCS). The flow field-flow fractionation (FlFFF) fractograms in combination with multi-angle light scattering (MALS) allowed an easy detection of maximum particle sizes what is most important for parenteral systems. Furthermore, high quality size distributions were received due to the separation step prior to size characterization. The calculated average size values exhibited a good correlation with z-averages determined by PCS. Only for suspensions of broader size distributions, higher deviations were observed. Comparing particle sizes with and without Poloxamer, differences in diameters resulted that were quantified. The additional Poloxamer shell was not able to be removed by an intensive washing during FlFFF focusing and separation. Especially FlFFF/MALS proved to be a valuable tool to characterize the pharmaceutical nanosuspensions in detail what is of great importance especially for controlled drug delivery systems.
聚(d,l-丙交酯-共-乙交酯)纳米悬浮液作为静脉注射纳米球系统,是通过在泊洛沙姆188水溶液中进行溶剂沉积制备的。将光散射技术应用于这些胶体系统以表征粒径。通过冷冻断裂复型和小角X射线散射(SAXS)证明得到了形状规则的球形颗粒。SAXS使用强同步辐射进行。根据散射曲线的小角部分计算粒径,其与从光子相关光谱法(PCS)获得的z平均值高度吻合。流场-流分级(FlFFF)分馏图与多角度光散射(MALS)相结合,便于检测最大粒径,这对肠胃外给药系统至关重要。此外,由于在粒径表征之前的分离步骤,获得了高质量的粒径分布。计算得到 的平均粒径值与通过PCS测定的z平均值具有良好的相关性。仅对于粒径分布较宽的悬浮液,观察到了较大的偏差。比较有无泊洛沙姆时的粒径,对所产生的直径差异进行了量化。在FlFFF聚焦和分离过程中,通过强力洗涤无法去除额外的泊洛沙姆壳。特别是FlFFF/MALS被证明是详细表征药物纳米悬浮液的宝贵工具,这对于控释给药系统尤为重要。