Mammalian cells cultured on 2D surfaces in microfluidic channels are increasingly used in drug development and biological research applications. These systems would have more biological or clinical relevance if the cells exhibit 3D phenotypes similar to the cells in vivo. We have developed a microfluidic channel based system that allows cells to be perfusion-cultured in 3D by supporting them with adequate 3D cell-cell and cell-matrix interactions. The maximal cell-cell interaction was achieved by perfusion-seeding cells through an array of micropillars; and 3D cell-matrix interactions were achieved by a polyelectrolyte complex coacervation process to form a thin layer of matrix conforming to the 3D cell shapes. Carcinoma cell lines (HepG2, MCF7), primary differentiated (hepatocytes) and primary progenitor cells (bone marrow mesenchymal stem cells) were perfusion-cultured for 72 hours to 1 week in the microfluidic channel, which preserved their 3D cyto-architecture and cell-specific functions or differentiation competence. This transparent 3D microfluidic channel-based cell culture system also allows direct optical monitoring of cellular events for a wide range of applications.

This paper reports on the comparison analysis of four main types of silicon-based microfilter for isolation of white blood cells (WBCs) from red blood cells (RBCs) in a given whole blood. The microfilter designs, namely, weir, pillar, crossflow, and membrane, all impose the same cut-off size of 3.5 mum to selectively trap WBCs. Using human whole blood, the microfilters have been characterized and compared for their blood handling capacity, WBCs trapping efficiency and RBCs passing efficiency. Based on the experimental results, the crossflow microfilter is superior and can be integrated with downstream components for on-chip genomic analysis.

The extraordinary climbing skills of gecko lizards have been under investigation for a long time. Here we report results of direct measurement of single spatula forces in air with varying relative humidities and in water, by the force-distance method using an atomic force microscope. We have found that the presence of water strongly affects the adhesion force and from analysis of our results, we have demonstrated that the dominant force involved is the capillary force.

Wafer‐scale polymer nanofabrillar structures have been fabricated using the combination of colloidal nanolithography, deep‐silicon etching, and nanomolding to mimic the nanostructure of gecko foot‐hairs. The artificial surface features densely packed polymeric nanofibrils with super‐hydrophobic, water‐repellent, and “easy‐to‐clean” characteristics. The lateral dimension of the nanofibrils is as small as 250 nm and an aspect‐ratio as high as 10:1 has been achieved without lateral collapse between neighboring fibrils. The method allows both fabrication of synthetic structures over a large area and direct integration of a flexible membrane to assist the array of nanofibrils in making intimate contact with uneven surfaces. A single nanofibril exhibits a mean adhesive force ranging from (0.91 ± 0.34) nN to (1.35 ± 0.37) nN. In the macroscopic scale, the nanostructured surface can adhere firmly to a smooth glass substrate and inherits the in‐use, self‐cleaning property of the setal nanostructures found in gecko lamellae.