A DNA optical sensor system is proposed based on the combination of sa
ndwich solution hybridization, magnetic bead capture, flow injection a
nd chemiluminescence for rapid detection of DNA hybridization. Bacteri
al alkaline phosphatase (phoA) gene and Hepatitis B virus (HBV) DNA we
re used as target DNA. A biotinylated DNA probe was used to capture th
e target gene onto the streptavidin-coated magnetic beads and a calf i
ntestine alkaline phosphatase (CAP)-labelled DNA probe was used for su
bsequent enzymatic chemiluminescence detection. The detection cycle wa
s less than 30 min, excluding the DNA hybridization time, which was ab
out 100 min. Both the phoA gene and HBV DNA could be detected at picog
ramme or femtomole level. No response signal was obtained when target
DNA did not exist in the sample. Successive sample detection could be
made by removing the magnetic field and a washing step. (C) 1998 Elsev
ier Science S.A. All rights reserved.