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Online Monitoring of PLGA Microparticles Formation Using Lasentec Focused Beam Reflectance (FBRM) and Particle Video Microscope (PVM)

机译:使用Lasentec聚焦光束反射率(FBRM)和粒子视频显微镜(PVM)在线监测PLGA微粒的形成

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摘要

Knowledge of the effects of different product and process variability on microparticle characterization is essential for the successful development, optimization, and scale-up of an encapsulation process. In the current research, the qualitative application of the Lasentec focused beam reflectance (FBRM) system for online monitoring of microparticle size distribution was demonstrated. lasentec particle vision and measurement (PVM) images were also employed to follow up the steps of microparticle formation and ripening. The drug entrapment efficiency and drug release characteristics were found to be dependent on the polymer, drug, and surfactant concentrations. DSC, FTIR, and XRD data revealed that the drug was compatible with the matrix forming polymer in the solid state. As indicated from the chord count data, FBRM was sensitive to the amount of the solid materials and the number of microparticles formed. Linear relationships with good correlations were obtained between polymer, drug, and surfactant levels and the disappearance rate of 5 to 36.8, 18.4 to 135.9, and 63 to 398 µm chord length fractions. Upon organic solvent evaporation, PVM imaging detected various stages of microemulsion droplets, sheath formation, and solidification with subsequent microparticle hardening. This study illustrated the utility of FBRM and PVM in monitoring the progress of particle formation during drug encapsulation.
机译:了解不同产品和工艺变异性对微粒表征的影响,对于成功开发,优化和扩大封装工艺至关重要。在当前的研究中,证明了Lasentec聚焦光束反射率(FBRM)系统在在线监测微粒尺寸分布方面的定性应用。还使用了lasentec粒子视觉和测量(PVM)图像来跟踪微粒形成和成熟的步骤。发现药物的包封效率和药物释放特性取决于聚合物,药物和表面活性剂的浓度。 DSC,FTIR和XRD数据表明该药物与固态形式的基质形成聚合物相容。如和弦计数数据所示,FBRM对固体材料的数量和形成的微粒数量敏感。聚合物,药物和表面活性剂水平之间的线性关系具有良好的相关性,并且弦长分数的消失率为5至36.8、18.4至135.9和63至398 µm。有机溶剂蒸发后,PVM成像检测到微乳液液滴,皮层形成以及随后的微粒硬化固化的各个阶段。这项研究说明了FBRM和PVM在监测药物封装过程中颗粒形成过程中的实用性。

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