A microchamber array for PCR was developed by semiconductor microfabricatio
n technology. The microchambers were designed to be of picoliter quantity.
To optimize fluid retention, the surface states of the substrate and the in
ner walls were examine for four different types of microchamber. The substr
ate was silicon, while silicon dioxide was selected for the inner walls. PC
R was performed in the microchamber array, and the amplification of DNA was
detected using a technique based on the energy transfer of fluorescent dye
s. The lower volume limit for PCR was investigated using various sizes of m
icrochambers. Microchambers with volume greater than 86 pL gave successful
PCR. In addition, the system was improved in order to take up the PCR produ
ct, To prevent mixing of the samples, the samples were dried after PCR usin
g a membrane that permeates only vapor.