TY - JOUR
T1 - Magnetic graphene oxide nanocomposite as dual-mode genosensor for ultrasensitive detection of oncogenic microRNA
AU - Kabinsing, Pinpinut
AU - Malla, Pravanjan
AU - Liu, Chi Hsien
AU - Wu, Wei Chi
AU - Sreearunothai, Paiboon
N1 - Publisher Copyright:
© 2023
PY - 2023/8
Y1 - 2023/8
N2 - MicroRNA (miRNA) is a noncoding RNA that controls cellular functions and gene expression. Several oncogenic miRNAs that aberrantly expressed in prostate cancer have the potential to be used as biomarkers. We designed multifunctional nanosheets that can capture, detect, and quantify miRNA 183-5p from prostate cancer cells with the aid of a disposable printed electrode and a portable potentiostat. Magnetic reduced graphene oxide (MrGO) has been used as the starting nanocomposite to analyze miRNA. Three cationic dyes—toluidine blue (TBO), thionine, and neutral red—were used to modify MrGO and evaluate its impact on the electron transfer rate. MrGO modified with TBO had the fastest conductivity and a large electrochemically active surface area. Two strategies were used to detect miRNA. One used peroxidase-labeled amplification and the other used TBO as the redox probe intercalating in the miRNA-capture probe duplex. The intercalator method reduced the complications of using peroxidase-labeled probes and exhibited superior performance. The limits of miRNA detection in human serum and urine were 3.73 and 0.86 aM, respectively, with a linear range from 0.1 nM to over 1 aM. The assay time of the intercalator method, including wash, was less than 16 min, and only one sample droplet (5 μL) was needed for analysis. We provided dual-mode genosensors for miRNA detection, which might be used for point-of-care testing. The incorporation of MrGO, screen-printed carbon electrodes, and portable potentiostat can accelerate biomarker detection, simplify analysis, and reduce the time and cost of analysis.
AB - MicroRNA (miRNA) is a noncoding RNA that controls cellular functions and gene expression. Several oncogenic miRNAs that aberrantly expressed in prostate cancer have the potential to be used as biomarkers. We designed multifunctional nanosheets that can capture, detect, and quantify miRNA 183-5p from prostate cancer cells with the aid of a disposable printed electrode and a portable potentiostat. Magnetic reduced graphene oxide (MrGO) has been used as the starting nanocomposite to analyze miRNA. Three cationic dyes—toluidine blue (TBO), thionine, and neutral red—were used to modify MrGO and evaluate its impact on the electron transfer rate. MrGO modified with TBO had the fastest conductivity and a large electrochemically active surface area. Two strategies were used to detect miRNA. One used peroxidase-labeled amplification and the other used TBO as the redox probe intercalating in the miRNA-capture probe duplex. The intercalator method reduced the complications of using peroxidase-labeled probes and exhibited superior performance. The limits of miRNA detection in human serum and urine were 3.73 and 0.86 aM, respectively, with a linear range from 0.1 nM to over 1 aM. The assay time of the intercalator method, including wash, was less than 16 min, and only one sample droplet (5 μL) was needed for analysis. We provided dual-mode genosensors for miRNA detection, which might be used for point-of-care testing. The incorporation of MrGO, screen-printed carbon electrodes, and portable potentiostat can accelerate biomarker detection, simplify analysis, and reduce the time and cost of analysis.
KW - Intercalator
KW - Magnetic reduced graphene oxide
KW - Peroxidase
KW - microRNA detection
UR - http://www.scopus.com/inward/record.url?scp=85153221551&partnerID=8YFLogxK
U2 - 10.1016/j.microc.2023.108775
DO - 10.1016/j.microc.2023.108775
M3 - 文章
AN - SCOPUS:85153221551
SN - 0026-265X
VL - 191
JO - Microchemical Journal
JF - Microchemical Journal
M1 - 108775
ER -