Lamprecht A, Schäfer U, Lehr C M
Department of Biopharmaceutics and Pharmaceutical Technology, Saarland University, Im Stadtwald, D-66123 Saarbrücken, Germany.
AAPS PharmSciTech. 2000 Jun 23;1(3):E17. doi: 10.1208/pt010317.
This study demonstrates the potential of confocal laser scanning microscopy (CLSM) as a characterization tool for different types of microparticles. Microparticles were prepared by various methods including complex coacervation, spray drying, double emulsion solvent evaporation technique, and ionotropic gelation. Protein drugs and particle wall polymers were covalently labeled with a fluorescent marker prior to particle preparation, while low molecular weight drugs were labeled by mixing with a fluorescent marker of similar solubility properties. As was demonstrated in several examples, CLSM allowed visualization of the polymeric particle wall composition and detection of heterogeneous polymer distribution or changes in polymer matrix composition under the influence of the drug. Furthermore, CLSM provides a method for three-dimensional reconstruction and image analysis of the microparticles by imaging several coplanar sections throughout the object. In conclusion, CLSM allows the inspection of internal particle structures without prior sample destruction. It can be used to localize the encapsulated compounds and to detect special structural details of the particle wall composition.
本研究证明了共聚焦激光扫描显微镜(CLSM)作为不同类型微粒表征工具的潜力。微粒通过多种方法制备,包括复凝聚法、喷雾干燥法、双乳液溶剂蒸发技术和离子凝胶法。在制备微粒之前,蛋白质药物和粒子壁聚合物用荧光标记物进行共价标记,而低分子量药物则通过与具有相似溶解特性的荧光标记物混合进行标记。正如在几个例子中所证明的,CLSM能够可视化聚合物粒子壁的组成,并检测药物影响下聚合物分布的不均匀性或聚合物基质组成的变化。此外,CLSM通过对整个物体的多个共面切片进行成像,提供了一种对微粒进行三维重建和图像分析的方法。总之,CLSM允许在不事先破坏样品的情况下检查粒子内部结构。它可用于定位包封的化合物,并检测粒子壁组成的特殊结构细节。