Microsystems Engineering, Rochester Institute of Technology, Rochester, New York 14623, USA.
Langmuir. 2012 Sep 18;28(37):13143-8. doi: 10.1021/la3025952. Epub 2012 Sep 4.
Microfluidic approaches for controlled generation of colloidal clusters, for example, via encapsulation of colloidal particles in droplets, have been used for the synthesis of functional materials including drug delivery carriers. Most of the studies, however, use a low concentration of an original colloidal suspension (<10 wt %). Here we demonstrate microfluidic approaches for directly making droplets with moderate (10-25 wt %) and high (>60 wt %) particle concentrations. Three types of microfluidic devices, PDMS flow-focusing, PDMS T-junction, and microcapillary devices, are investigated for direct encapsulation of a high concentration of polystyrene (PS) nanoparticles in droplets. In particular, it is shown that PDMS devices fabricated by soft lithography can generate droplets from a 25 wt % PS suspension, whereas microcapillary devices made from glass capillary tubes are able to produce droplets from a 67 wt % PS nanoparticle suspension. When the PS concentration is between 0.6 and 25 wt %, the size of the droplets is found to change with the oil-to-water flow rate ratio and is independent of the concentration of particles in the initial suspensions. Drop sizes from ~12 to 40 μm are made using flow rate ratios Q(oil)/Q(water) from 20 to 1, respectively, with either of the PDMS devices. However, clogging occurs in PDMS devices at high PS concentrations (>25 wt %) arising from interactions between the PS colloids and the surface of PDMS devices. Glass microcapillary devices, on the other hand, are resistant to clogging and can produce droplets continuously even when the concentration of PS nanoparticles reaches 67 wt %. We believe that our findings indicate useful approaches and guidelines for the controlled generation of emulsions filled with a high loading of nanoparticles, which are useful for drug delivery applications.
微流控方法可用于控制胶体簇的生成,例如通过将胶体颗粒封装在液滴中,已被用于合成包括药物输送载体在内的功能材料。然而,大多数研究使用低浓度的原始胶体悬浮液(<10wt%)。在这里,我们展示了用于直接制备中等(10-25wt%)和高(>60wt%)颗粒浓度的液滴的微流控方法。研究了三种微流控装置,PDMS 流聚焦、PDMS T 型接头和微毛细管装置,用于直接封装高浓度的聚苯乙烯(PS)纳米颗粒在液滴中。特别是,结果表明,通过软光刻制造的 PDMS 器件可以从 25wt%PS 悬浮液中生成液滴,而由玻璃毛细管制成的微毛细管装置能够从 67wt%PS 纳米颗粒悬浮液中生成液滴。当 PS 浓度在 0.6 和 25wt%之间时,发现液滴的大小随油-水流量比而变化,并且与初始悬浮液中颗粒的浓度无关。使用 PDMS 装置,分别使用 Q(油)/Q(水)的流量比从 20 到 1 来制备尺寸为~12 至 40μm的液滴。然而,在高 PS 浓度(>25wt%)下,PDMS 装置中会发生堵塞,这是由于 PS 胶体与 PDMS 装置表面之间的相互作用引起的。另一方面,玻璃微毛细管装置不易堵塞,即使 PS 纳米颗粒的浓度达到 67wt%,也可以连续产生液滴。我们相信,我们的发现为控制填充有高负载纳米颗粒的乳液的生成提供了有用的方法和指导,这对于药物输送应用是有用的。