TY - JOUR
T1 - Fungal pathogenic nucleic acid detection achieved with a microfluidic microarray device
AU - Wang, Lin
AU - Li, Paul C.H.
AU - Yu, Hua-Zhong
AU - Parameswaran, Ash M.
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2008/3/3
Y1 - 2008/3/3
N2 - Detection of polymerase chain reaction (PCR) products obtained from cultured greenhouse fungal pathogens, Botrytis cinerea and Didymella bryoniae has been achieved using a previously developed microfluidic microarray assembly (MMA) device. The flexible probe construction and rapid DNA detection resulted from the use of centrifugal pumping in the steps of probe introduction and sample delivery, respectively. The line arrays of the oligonucleotide probes were "printed" on a CD-like glass chip using a polydimethylsiloxane (PDMS) polymer plate with radial microfluidic channels, and the sample hybridizations were conducted within the spiral channels on the second plate. The experimental conditions of probe immobilization and sample hybridization were optimized, and both complementary oligonucleotides and PCR products were tested. We were able to achieve adequate fluorescent signals with a sample load as small as 0.5 nM (1 μL) for oligonucleotide samples; for PCR products, we achieved detection at the level of 3 ng. © 2008 Elsevier B.V. All rights reserved.
AB - Detection of polymerase chain reaction (PCR) products obtained from cultured greenhouse fungal pathogens, Botrytis cinerea and Didymella bryoniae has been achieved using a previously developed microfluidic microarray assembly (MMA) device. The flexible probe construction and rapid DNA detection resulted from the use of centrifugal pumping in the steps of probe introduction and sample delivery, respectively. The line arrays of the oligonucleotide probes were "printed" on a CD-like glass chip using a polydimethylsiloxane (PDMS) polymer plate with radial microfluidic channels, and the sample hybridizations were conducted within the spiral channels on the second plate. The experimental conditions of probe immobilization and sample hybridization were optimized, and both complementary oligonucleotides and PCR products were tested. We were able to achieve adequate fluorescent signals with a sample load as small as 0.5 nM (1 μL) for oligonucleotide samples; for PCR products, we achieved detection at the level of 3 ng. © 2008 Elsevier B.V. All rights reserved.
KW - Centrifugal pumping
KW - Fungal pathogen
KW - Microfluidic microarray
KW - Nucleic acid hybridization
KW - Centrifugal pumping
KW - Fungal pathogen
KW - Microfluidic microarray
KW - Nucleic acid hybridization
KW - Centrifugal pumping
KW - Fungal pathogen
KW - Microfluidic microarray
KW - Nucleic acid hybridization
UR - http://www.scopus.com/inward/record.url?scp=39149102468&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-39149102468&origin=recordpage
U2 - 10.1016/j.aca.2007.12.048
DO - 10.1016/j.aca.2007.12.048
M3 - RGC 21 - Publication in refereed journal
C2 - 18267145
SN - 0003-2670
VL - 610
SP - 97
EP - 104
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
IS - 1
ER -