Díaz-López Raquel, Tsapis Nicolas, Libong Danielle, Chaminade Pierre, Connan Carole, Chehimi Mohamed M, Berti Romain, Taulier Nicolas, Urbach Wladimir, Nicolas Valérie, Fattal Elias
Univ. Paris Sud, UMR CNRS 8612, IFR 141, Faculté de Pharmacie, 5 Rue Jean-Baptiste Clément, Châtenay-Malabry, France.
Biomaterials. 2009 Mar;30(8):1462-72. doi: 10.1016/j.biomaterials.2008.11.032. Epub 2008 Dec 20.
We present here an easy method to modify the surface chemistry of polymeric microcapsules of perfluorooctyl bromide used as ultrasound contrast agents (UCAs). Capsules were obtained by a solvent emulsification-evaporation process with phospholipids incorporated in the organic phase before emulsification. Several phospholipids were reviewed: fluorescent, pegylated and biotinylated phospholipids. The influence of phospholipid concentration on microcapsule size and morphology was evaluated. Only a fraction of the phospholipids is associated to microcapsules, the rest being dissolved with the surfactant in the aqueous phase. Microscopy shows that phospholipids are present within the shell and that the core/shell structure is preserved up to 0.5 mg fluorescent phospholipids, up to about 0.25 mg pegylated phospholipids or biotinylated phospholipids (for 100 mg of polymer, poly(lactide-co-glycolide) (PLGA)). HPLC allows quantifying phospholipids associated to capsules: they correspond to 10% of pegylated phospholipids introduced in the organic phase. The presence of pegylated lipids at the surface of capsules was confirmed by X-ray photon electron spectroscopy (XPS). The pegylation did not modify the echographic signal arising from capsules. Finally biotinylated microcapsules incubated with neutravidin tend to aggregate, which confirms the presence of biotin at the surface. These results are encouraging and future work will consist of nanocapsule surface modification for molecular imaging.
我们在此展示一种简便方法,用于修饰用作超声造影剂(UCAs)的全氟辛基溴化聚合物微胶囊的表面化学性质。微胶囊通过溶剂乳化-蒸发法制备,在乳化前将磷脂掺入有机相中。研究了几种磷脂:荧光磷脂、聚乙二醇化磷脂和生物素化磷脂。评估了磷脂浓度对微胶囊尺寸和形态的影响。只有一部分磷脂与微胶囊相关联,其余部分与表面活性剂一起溶解在水相中。显微镜检查表明,磷脂存在于壳层内,并且在高达0.5 mg荧光磷脂、高达约0.25 mg聚乙二醇化磷脂或生物素化磷脂(对于100 mg聚合物,聚(丙交酯-共-乙交酯)(PLGA))的情况下,核/壳结构得以保留。高效液相色谱法可对与微胶囊相关的磷脂进行定量:它们相当于引入有机相中的聚乙二醇化磷脂的10%。通过X射线光电子能谱(XPS)证实了微胶囊表面存在聚乙二醇化脂质。聚乙二醇化并未改变微胶囊产生的超声信号。最后,用中性抗生物素蛋白孵育生物素化微胶囊会趋于聚集,这证实了表面存在生物素。这些结果令人鼓舞,未来的工作将包括用于分子成像的纳米胶囊表面修饰。