Handheld ISFET Lab-on-Chip Detection of TMPRSS2-ERG and AR mRNA for Prostate Cancer Prognostics

被引:0
作者
Broomfield, Joseph [1 ,2 ]
Kalofonou, Melpomeni [1 ]
Franklin, Sylvia [1 ]
Powell, Sue M. [2 ]
Pataillot-Meakin, Thomas [2 ,3 ,4 ]
Moser, Nicolas [1 ]
Bevan, Charlotte L. [2 ]
Georgiou, Pantelis [1 ]
机构
[1] Imperial Coll London, Ctr BioInspired Technol Elect & Elect Engn, London SW7 2AZ, England
[2] Imperial Coll London, Imperial Ctr Translat & Expt Med, Dept Surg & Canc, London W12 0NN, England
[3] Imperial Coll London, Dept Chem, Mol Sci Res Hub, London W12 0NN, England
[4] Imperial Coll London, Dept Bioengn, Sir Michael Uren Hub, London W12 0BZ, England
关键词
Chemical and biological sensors; biosensors; ion-sensitive field-effect transistors (ISFETs); lab-on-chip; prostate cancer; RNA; reverse transcriptase loop-mediated isothermal amplification (RT-LAMP); ANDROGEN RECEPTOR; ACTIVE SURVEILLANCE; CELL-PROLIFERATION; GENE FUSION; DNA; AMPLIFICATION;
D O I
10.1109/LSENS.2023.3296395
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Ion-sensitive field-effect transistors (ISFETs), in combination with unmodified complementary metal oxide semiconductors, present a point-of-care platform for clinical diagnostics and prognostics. This work illustrates the sensitive and specific detection of two circulating mRNA markers for prostate cancer: the androgen receptor and the TMPRSS2-ERG fusion using a target-specific loop-mediated isothermal amplification method. TMPRSS2-ERG and androgen receptor RNA were detected down to 3 x10(1) and 5 x10(1) copies, respectively, in under 30 min. Administration of these assays onto the ISFET lab-on-chip device was successful and the specificity of each marker was corroborated with mRNA extracted from prostate cancer cell lines.
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页数:4
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