...
首页> 外文期刊>Lab on a chip >A flow-free droplet-based device for high throughput polymorphic crystallization
【24h】

A flow-free droplet-based device for high throughput polymorphic crystallization

机译:基于无液滴的高通量多晶型结晶装置

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Crystallization is one of the most crucial steps in the process of pharmaceutical formulation. In recent years, emulsion-based platforms have been developed and broadly adopted to generate high quality products. However, these conventional approaches such as stirring are still limited in several aspects, e.g., unstable crystallization conditions and broad size distribution; besides, only simple crystal forms can be produced. In this paper, we present a new flow-free droplet-based formation process for producing highly controlled crystallization with two examples: (1) NaCl crystallization reveals the ability to package saturated solution into nanoliter droplets, and (2) glycine crystallization demonstrates the ability to produce polymorphic crystallization forms by controlling the droplet size and temperature. In our process, the saturated solution automatically fills the microwell array powered by degassed bulk PDMS. A critical oil covering step is then introduced to isolate the saturated solution and control the water dissolution rate. Utilizing surface tension, the solution is uniformly packaged in the form of thousands of isolating droplets at the bottom of each microwell of 50-300 mu m diameter. After water dissolution, individual crystal structures are automatically formed inside the microwell array. This approach facilitates the study of different glycine growth processes: alpha-form generated inside the droplets and gamma-form generated at the edge of the droplets. With precise temperature control over nanoliter-sized droplets, the growth of ellipsoidal crystalline agglomerates of glycine was achieved for the first time. Optical and SEM images illustrate that the ellipsoidal agglomerates consist of 2-5 mu m glycine clusters with inner spiral structures of similar to 35 mu m screw pitch. Lastly, the size distribution of spherical crystalline agglomerates (SAs) produced from microwells of different sizes was measured to have a coefficient variation (CV) of less than 5%, showing crystal sizes can be precisely controlled by microwell sizes with high uniformity. This new method can be used to reliably fabricate monodispersed crystals for pharmaceutical applications.
机译:结晶是药物配制过程中最关键的步骤之一。近年来,基于乳液的平台已经开发并被广泛采用以生成高质量的产品。但是,这些常规方法如搅拌仍在几个方面受到限制,例如,不稳定的结晶条件和宽的粒度分布。此外,只能产生简单的晶体形式。在本文中,我们通过两个示例介绍了一种用于产生高度受控的结晶的,基于无液滴的新形成过程:(1)NaCl结晶显示了将饱和溶液包装成纳升液滴的能力,(2)甘氨酸结晶证明了该能力通过控制液滴的大小和温度来产生多晶型结晶形式。在我们的过程中,饱和溶液会自动填充由脱气散装PDMS驱动的微孔阵列。然后引入关键的油覆盖步骤以分离饱和溶液并控制水溶解速率。利用表面张力,将溶液以数千个分离液滴的形式均匀包装在直径为50-300μm的每个微孔的底部。溶解后,微孔阵列内部会自动形成单个晶体结构。这种方法有助于研究不同的甘氨酸生长过程:液滴内部产生的α形式和液滴边缘产生的γ形式。通过对纳升大小的液滴进行精确的温度控制,首次实现了甘氨酸的椭圆形结晶附聚物的生长。光学和SEM图像表明,椭圆形附聚物由2-5μm的甘氨酸簇组成,其内部螺旋结构类似于35μm的螺距。最后,测量了由不同尺寸的微孔产生的球形晶体附聚物(SA)的尺寸分布,其系数变化(CV)小于5%,表明可以通过具有高均匀度的微孔尺寸精确控制晶体尺寸。这种新方法可用于可靠地制造用于制药应用的单分散晶体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号