Fast screening of bacterial suspension culture conditions on chips.

Culture conditions including pH, nutrient concentration and temperature strongly influence the properties of a microbial strain by affecting many factors such as the microbial membrane and metabolism. We present a microfluidic chip for screening pH and nutrient content with a concentration gradient generator connected to eight parallel suspension culture loops and another chip for the screening of temperature with four different temperature zones under suspension culture loops. Bacteria grow much faster on chips than in test tubes, and yet interestingly, on-chip screening of culture conditions for E. coli yields results similar to those from a culture in test tubes, demonstrating the validity of the on-chip screening approach. The microfluidic chips were applied to study the growth conditions of two wild type Bacillus subtilis strains isolated from polluted water. The on-chip screening experiments show advantages of nanoliter scale screening units, high-throughput and requiring only one-fourth of the time.

Two dimensional barcode-inspired automatic analysis for arrayed microfluidic immunoassays.

The usability of many high-throughput lab-on-a-chip devices in point-of-care applications is currently limited by the manual data acquisition and analysis process, which are labor intensive and time consuming. Based on our original design in the biochemical reactions, we proposed here a universal approach to perform automatic, fast, and robust analysis for high-throughput array-based microfluidic immunoassays. Inspired by two-dimensional (2D) barcodes, we incorporated asymmetric function patterns into a microfluidic array. These function patterns provide quantitative information on the characteristic dimensions of the microfluidic array, as well as mark its orientation and origin of coordinates. We used a computer program to perform automatic analysis for a high-throughput antigen/antibody interaction experiment in 10 s, which was more than 500 times faster than conventional manual processing. Our method is broadly applicable to many other microchannel-based immunoassays.

Towards a high-throughput label-free detection system combining localized-surface plasmon resonance and microfluidics.

This work reports an integrated platform combining localized-surface plasmon resonance (LSPR) and microfluidic chips to carry out multiplexed and label-free protein analysis. We fabricated an optical bench to enable detection using only a laboratory UV-Vis spectrophotometer. This assay not only improves throughput, but also allows quantitative analysis.