A digital microfluidic droplet generator produces self-assembled supramolecular nanoparticles for targeted cell imaging

• Published in: Nanotechnology Vol. 21; no. 44; p. 445603
• Main Authors: Liu, Kan, Wang, Hao, Chen, Kuan-Ju, Guo, Feng, Lin, Wei-Yu, Chen, Yi-Chun, Phung, Duy Linh, Tseng, Hsian-Rong, Shen, Clifton K-F
• Format: Journal Article
• Language: English
• Published: England 05.11.2010
• Subjects: Cell Line, Tumor; Chips; Digital; Dimethylpolysiloxanes - chemistry; Droplets; Generators; Humans; Imaging, Three-Dimensional - methods; Microfluidic Analytical Techniques - instrumentation; Microfluidics; Nanoparticles; Nanoparticles - chemistry; Nanoparticles - ultrastructure; Oligopeptides - metabolism; Particle Size; Size distribution; Tasks; Time Factors
• ISSN: 0957-4484; 1361-6528
• DOI: 10.1088/0957-4484/21/44/445603

Controlling the size distribution of polymer-based nanoparticles is a challenging task due to their flexible core and surface structures. To accomplish such as task requires very precise control at the molecular level. Here we demonstrate a new approach whereby uniform-sized supramolecular nanoparticles (SNPs) can be reliably generated using a digital microfluidic droplet generator (DMDG) chip. A microfluidic environment enabled precise control over the processing parameters, and therefore high batch-to-batch reproducibility and robust production of SNPs with a very narrow size distribution could be realized. Digitally adjustment of the mixing ratios of the building blocks on the DMDG chip allowed us to rapidly scan a variety of synthesis conditions without consuming significant amounts of reagents. Nearly uniform SNPs with sizes ranging from 35 to 350 nm were obtained and characterized by transmission electron microscopy and dynamic light scattering. In addition, we could fine-tune the surface chemistry of the SNPs by incorporating an additional building block functionalized with specific ligands for targeting cells. The sizes and surface properties of these SNPs correlated strongly with their cell uptake efficiencies. This study showed a feasible method for microfluidic-assisted SNP production and provided a great means for preparing size-controlled SNPs with desired surface ligand coverage.