TY - JOUR
T1 - Passive direct methanol fuel cells acting as fully autonomous electrochemical biosensors
T2 - Application to sarcosine detection
AU - Ferreira, Nádia S.
AU - Carneiro, Liliana P.T.
AU - Viezzer, Christian
AU - Almeida, Maria J. T.
AU - Marques, Ana C.
AU - Pinto, Alexandra M. F. R.
AU - Fortunato, Elvira
AU - Sales, M. Goreti F.
N1 - info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0037%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50025%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50025%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FEMS%2F00532%2F2019/PT#
info:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F122955%2F2016/PT#
info:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F122954%2F2016/PT#
info:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F115173%2F2016/PT#
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/10/1
Y1 - 2022/10/1
N2 - This work describes an innovative electrochemical biosensor that advances its autonomy toward an equipment-free design. The biosensor is powered by a passive direct methanol fuel cell (DMFC) and signals the response via an electrochromic display. Briefly, the anode side of the DMFC power source was modified with a biosensor layer developed using molecularly imprinted polymer (MIP) technology to detect sarcosine (an amino acid derivative that is a potential cancer biomarker). The biosensor layer was anchored on the surface of the anode carbon electrode (carbon black with Pt/Ru, 40:20). This was done by bulk radical polymerization with acrylamide, bis-acrylamide, and vinyl phosphonic acid. This layer selectively interacted with sarcosine when integrated into the passive DMFC (single or multiple, in a stack of 4), which acted as a transducer element in a concentration-dependent process. Serial assembly of a stack of hybrid DMFC/biosensor devices triggered an external electrochromic cell (EC) that produced a colour change. Calibrations showed a concentration-dependent sarcosine response from 3.2 to 2000 µM, which is compatible with the concentration of sarcosine in the blood of prostate cancer patients. The final DMFC/biosensor-EC platform showed a colour change perceptible to the naked eye in the presence of increasing sarcosine concentrations. This colour change was controlled by the DMFC operation, making this approach a self-controlled and self-signalling device. Overall, this approach is a proof-of-concept for a fully autonomous biosensor powered by a chemical fuel. This simple and low-cost approach offers the potential to be deployed anywhere and is particularly suitable for point-of-care (POC) analysis.
AB - This work describes an innovative electrochemical biosensor that advances its autonomy toward an equipment-free design. The biosensor is powered by a passive direct methanol fuel cell (DMFC) and signals the response via an electrochromic display. Briefly, the anode side of the DMFC power source was modified with a biosensor layer developed using molecularly imprinted polymer (MIP) technology to detect sarcosine (an amino acid derivative that is a potential cancer biomarker). The biosensor layer was anchored on the surface of the anode carbon electrode (carbon black with Pt/Ru, 40:20). This was done by bulk radical polymerization with acrylamide, bis-acrylamide, and vinyl phosphonic acid. This layer selectively interacted with sarcosine when integrated into the passive DMFC (single or multiple, in a stack of 4), which acted as a transducer element in a concentration-dependent process. Serial assembly of a stack of hybrid DMFC/biosensor devices triggered an external electrochromic cell (EC) that produced a colour change. Calibrations showed a concentration-dependent sarcosine response from 3.2 to 2000 µM, which is compatible with the concentration of sarcosine in the blood of prostate cancer patients. The final DMFC/biosensor-EC platform showed a colour change perceptible to the naked eye in the presence of increasing sarcosine concentrations. This colour change was controlled by the DMFC operation, making this approach a self-controlled and self-signalling device. Overall, this approach is a proof-of-concept for a fully autonomous biosensor powered by a chemical fuel. This simple and low-cost approach offers the potential to be deployed anywhere and is particularly suitable for point-of-care (POC) analysis.
KW - Cancer biomarker
KW - Colour display
KW - Electrochromic cell
KW - Molecularly imprinted polymer
KW - Passive direct methanol fuel cell
KW - Sarcosine
UR - http://www.scopus.com/inward/record.url?scp=85137165406&partnerID=8YFLogxK
U2 - 10.1016/j.jelechem.2022.116710
DO - 10.1016/j.jelechem.2022.116710
M3 - Article
AN - SCOPUS:85137165406
SN - 1572-6657
VL - 922
JO - Journal Of Electroanalytical Chemistry
JF - Journal Of Electroanalytical Chemistry
M1 - 116710
ER -