Zimmermann Anne, Elema Michiel Ringkjøbing, Hansen Tue, Müllertz Anette, Hovgaard Lars
Faculty of Pharmaceutical Sciences, Department of Pharmaceutics and Analytical Chemistry, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen Ø, Denmark.
J Pharm Biomed Anal. 2007 Aug 15;44(4):874-80. doi: 10.1016/j.jpba.2007.04.009. Epub 2007 Apr 19.
A common challenge in the development of new drug substances is poor dissolution characteristics related to low aqueous solubility. One approach to overcome this problem is antisolvent precipitation in the presence of polymers or surfactants, which may enhance the dissolution rate through reduced particle size and increased wettability. In this study, a simple method based on size exclusion chromatography (SEC) with evaporative light scattering detection (ELSD) was developed for the determination of polymers and surfactants adsorbed to drug particles prepared by antisolvent precipitation of the poorly water-soluble model drug Lu 28-179. Detection of many polymeric excipients and surfactants is problematic due to the lack of UV-absorbing chromophores, but ELSD proved successful for the direct determination of the investigated compounds. A mixed mode column was used to effectively separate each of the excipient structures from the drug. The mobile phase comprised acetonitrile-ammonium formate (20mM; pH 6.5) (50:50, v/v) at a flow-rate of 0.6 ml/min. Qualification studies showed that the method was adequately sensitive and precise with limits of detection between 0.72 and 4.32 microg/ml. Linearity of the calibration curves was achieved by log-log modelling. The method was applied for determination of nine polymeric excipients and surfactants adsorbed to particles of the model drug. The extent of excipient adsorption varied between 0.07 and 1.39% (w/w) of the total particle weight.
新药物研发中的一个常见挑战是与低水溶性相关的溶出特性较差。克服这一问题的一种方法是在聚合物或表面活性剂存在下进行抗溶剂沉淀,这可能通过减小粒径和增加润湿性来提高溶出速率。在本研究中,开发了一种基于尺寸排阻色谱(SEC)与蒸发光散射检测(ELSD)的简单方法,用于测定通过难溶性模型药物Lu 28 - 179的抗溶剂沉淀制备的药物颗粒上吸附的聚合物和表面活性剂。由于缺乏紫外吸收发色团,许多聚合物辅料和表面活性剂的检测存在问题,但ELSD被证明可成功直接测定所研究的化合物。使用混合模式柱有效地将每种辅料结构与药物分离。流动相由乙腈 - 甲酸铵(20mM;pH 6.5)(50:50,v/v)组成,流速为0.6 ml/min。鉴定研究表明,该方法具有足够的灵敏度和精密度,检测限在0.72至4.32 μg/ml之间。校准曲线的线性通过对数 - 对数建模实现。该方法用于测定吸附在模型药物颗粒上的九种聚合物辅料和表面活性剂。辅料的吸附程度在总颗粒重量的0.07%至1.39%(w/w)之间变化。