An integrated microfluidic system with field-effect-transistor sensor arrays for detecting multiple cardiovascular biomarkers from clinical samples

Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the use of multiple biomarkers for proper risk assessment of CVDs. Herein four such CVDs biomarkers- C-reactive protein (CRP), N-terminal pro b-...

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Published inBiosensors & bioelectronics Vol. 129; pp. 155 - 163
Main Authors Sinha, Anirban, Tai, Tse-Yu, Li, Kuang-Hsien, Gopinathan, Priya, Chung, Yi-Da, Sarangadharan, Indu, Ma, Hsi-Pin, Huang, Po-Chiun, Shiesh, Shu-Chu, Wang, Yu-Lin, Lee, Gwo-Bin
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 15.03.2019
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Abstract Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the use of multiple biomarkers for proper risk assessment of CVDs. Herein four such CVDs biomarkers- C-reactive protein (CRP), N-terminal pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTnI), and fibrinogen- were rapidly (5 min) analyzed from clinical samples (~ 4 µL) on an integrated microfluidic platform equipped with 1) immobilized highly specific aptamer probes and 2) field-effect transistor (FET)-based sensor arrays. The calibration curve from the FET sensor arrays showed good agreement in the physiological concentration ranges for CRP (0.1–50 mg/L), NT-proBNP (50–10,000 pg/mL), cTnI (1–10,000 pg/mL), and fibrinogen (0.1–5 mg/mL). The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in clinical samples. •An integrated microfluidic platform equipped with 1) immobilized aptamer probes and 2) field-effect transistor (FET)-based sensor arrays has been presented in this study.•Four biomarkers for cardiovascular diseases were rapidly (5 min) analyzed from clinical samples (~ 4 µL).•The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in patient serum.
AbstractList Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the use of multiple biomarkers for proper risk assessment of CVDs. Herein four such CVDs biomarkers- C-reactive protein (CRP), N-terminal pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTnI), and fibrinogen- were rapidly (5 min) analyzed from clinical samples (~ 4 µL) on an integrated microfluidic platform equipped with 1) immobilized highly specific aptamer probes and 2) field-effect transistor (FET)-based sensor arrays. The calibration curve from the FET sensor arrays showed good agreement in the physiological concentration ranges for CRP (0.1–50 mg/L), NT-proBNP (50–10,000 pg/mL), cTnI (1–10,000 pg/mL), and fibrinogen (0.1–5 mg/mL). The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in clinical samples.
Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the use of multiple biomarkers for proper risk assessment of CVDs. Herein four such CVDs biomarkers- C-reactive protein (CRP), N-terminal pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTnI), and fibrinogen- were rapidly (5 min) analyzed from clinical samples (~ 4 µL) on an integrated microfluidic platform equipped with 1) immobilized highly specific aptamer probes and 2) field-effect transistor (FET)-based sensor arrays. The calibration curve from the FET sensor arrays showed good agreement in the physiological concentration ranges for CRP (0.1–50 mg/L), NT-proBNP (50–10,000 pg/mL), cTnI (1–10,000 pg/mL), and fibrinogen (0.1–5 mg/mL). The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in clinical samples. •An integrated microfluidic platform equipped with 1) immobilized aptamer probes and 2) field-effect transistor (FET)-based sensor arrays has been presented in this study.•Four biomarkers for cardiovascular diseases were rapidly (5 min) analyzed from clinical samples (~ 4 µL).•The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in patient serum.
Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the use of multiple biomarkers for proper risk assessment of CVDs. Herein four such CVDs biomarkers- C-reactive protein (CRP), N-terminal pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTnI), and fibrinogen- were rapidly (5 min) analyzed from clinical samples (~ 4 µL) on an integrated microfluidic platform equipped with 1) immobilized highly specific aptamer probes and 2) field-effect transistor (FET)-based sensor arrays. The calibration curve from the FET sensor arrays showed good agreement in the physiological concentration ranges for CRP (0.1-50 mg/L), NT-proBNP (50-10,000 pg/mL), cTnI (1-10,000 pg/mL), and fibrinogen (0.1-5 mg/mL). The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in clinical samples.Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the use of multiple biomarkers for proper risk assessment of CVDs. Herein four such CVDs biomarkers- C-reactive protein (CRP), N-terminal pro b-type natriuretic peptide (NT-proBNP), cardiac troponin I (cTnI), and fibrinogen- were rapidly (5 min) analyzed from clinical samples (~ 4 µL) on an integrated microfluidic platform equipped with 1) immobilized highly specific aptamer probes and 2) field-effect transistor (FET)-based sensor arrays. The calibration curve from the FET sensor arrays showed good agreement in the physiological concentration ranges for CRP (0.1-50 mg/L), NT-proBNP (50-10,000 pg/mL), cTnI (1-10,000 pg/mL), and fibrinogen (0.1-5 mg/mL). The developed prototype of this fully automated portable device requires minimal reagent and sample inputs and consequently shows great promise for next-generation point-of-care devices assaying multiple CVDs biomarkers in clinical samples.
Author Chung, Yi-Da
Sinha, Anirban
Li, Kuang-Hsien
Tai, Tse-Yu
Shiesh, Shu-Chu
Gopinathan, Priya
Wang, Yu-Lin
Sarangadharan, Indu
Huang, Po-Chiun
Ma, Hsi-Pin
Lee, Gwo-Bin
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  fullname: Shiesh, Shu-Chu
  organization: Department of Medical Laboratory Science and Biotechnology, National Cheng Kung University, Tainan, Taiwan
– sequence: 10
  givenname: Yu-Lin
  surname: Wang
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  email: ylwang@mx.nthu.edu.tw
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Keywords CRP
cTnI
HEMT
TE buffer
EDL
AlGaN/GaN
NT-proBNP
SPR
ssDNA
SELEX
LOD
PBS
EMVs
EDTA
LCD
FET
PMMA
Field-effect transistors
Aptamers
Biomarkers
Cardiovascular diseases
CVDs
TCEP
Microfluidics
ELISA
PDMS
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Snippet Certain blood-borne biomarkers offer a potent methodology for understanding the risk of cardiovascular diseases (CVDs) with clinicians generally advocating the...
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SubjectTerms Aptamers
Biomarkers
biosensors
C-reactive protein
Cardiovascular diseases
fibrinogen
Field-effect transistors
Microfluidics
natriuretic peptides
oligonucleotides
point-of-care systems
portable equipment
prototypes
risk
transistors
troponin I
Title An integrated microfluidic system with field-effect-transistor sensor arrays for detecting multiple cardiovascular biomarkers from clinical samples
URI https://dx.doi.org/10.1016/j.bios.2019.01.001
https://www.ncbi.nlm.nih.gov/pubmed/30703568
https://www.proquest.com/docview/2179428016
https://www.proquest.com/docview/2189537008
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