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Projeto de investigação
Nanobiosensing platform based on MIP-SERS for breast cancer exosome characterization and detection
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Nanobiosensing platforms with sers and mip-based technologies
Publication . Marques, Ana Carolina Cardoso; Fortunato, Elvira; Sales, Maria Goreti; Costa-Silva, Bruno
Passive direct methanol fuel cells acting as fully autonomous electrochemical biosensors
Publication . Ferreira, Nádia S.; Carneiro, Liliana P.T.; Viezzer, Christian; Almeida, Maria J. T.; Marques, Ana C.; Pinto, Alexandra M. F. R.; Fortunato, Elvira; Sales, M. Goreti F.; UNINOVA-Instituto de Desenvolvimento de Novas Tecnologias; CENIMAT-i3N - Centro de Investigação de Materiais (Lab. Associado I3N); DCM - Departamento de Ciência dos Materiais; Elsevier Science B.V., Amsterdam.
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.
A Planar Electrochromic Device using WO3 Nanoparticles and a Modified Paper-Based Electrolyte
Publication . Marques, Ana; Santos, Lídia; Pereira, Sónia; Emanuele, Umberto; Sinopoli, Stefano; Igreja, Rui; Sales, Goreti; Martins, Rodrigo; Fortunato, Elvira; UNINOVA-Instituto de Desenvolvimento de Novas Tecnologias; CENIMAT-i3N - Centro de Investigação de Materiais (Lab. Associado I3N); DCM - Departamento de Ciência dos Materiais; MDPI - Multidisciplinary Digital Publishing Institute
Electrochromic devices are increasing its interest in the last decades due to the wide range of applications, from smart windows to biosensors or from smart labels to super-capacitors. So, the development of simple and cost-effective production technologies based on solution process and mask less approach is of great interest. In this work, a new planar and flexible electrochromic device based on tungsten oxide (WO3) nanoparticles with a paper-based modified electrolyte was successfully produced, using a CO2 laser technology for electrodes patterning and hydrothermal synthesis for the nanoparticles production. The devices were fabricated with a paper pad inserted in the sensor area for hydration on time of usage, thus replacing the electrolyte material of a typical electrochromic structure with a multi-layer stack, eliminating leakage problems, easy integration with other devices and enhancing the shelf life of the devices to several months. The produced device presents a low power consumption of only 2.86 μA·cm−2, with a deep blue color and an initial charge modulation of 11.5.
Paper-Based Biosensors for COVID-19
Publication . Pinheiro, Tomás; Cardoso, Ana Rita; Sousa, Cristina E. A.; Marques, Ana Carolina; Tavares, Ana P. M.; Matos, Ana Miguel; Cruz, Maria Teresa; Moreira, Felismina T. C.; Martins, Rodrigo; Fortunato, Elvira; Sales, M. Goreti F.; DCM - Departamento de Ciência dos Materiais; CENIMAT-i3N - Centro de Investigação de Materiais (Lab. Associado I3N); UNINOVA-Instituto de Desenvolvimento de Novas Tecnologias; ACS - American Chemical Society
The appearance and quick spread of the new severe acute respiratory syndrome coronavirus disease, COVID-19, brought major societal challenges. Importantly, suitable medical diagnosis procedures and smooth clinical management of the disease are an emergent need, which must be anchored on novel diagnostic methods and devices. Novel molecular diagnostic tools relying on nucleic acid amplification testing have emerged globally and are the current gold standard in COVID-19 diagnosis. However, the need for widespread testing methodologies for fast, effective testing in multiple epidemiological scenarios remains a crucial step in the fight against the COVID-19 pandemic. Biosensors have previously shown the potential for cost-effective and accessible diagnostics, finding applications in settings where conventional, laboratorial techniques may not be readily employed. Paper- and cellulose-based biosensors can be particularly relevant in pandemic times, for the renewability, possibility of mass production with sustainable methodologies, and safe environmental disposal. In this review, paper-based devices and platforms targeting SARS-CoV-2 are showcased and discussed, as a means to achieve quick and low-cost PoC diagnosis, including detection methodologies for viral genomic material, viral antigen detection, and serological antibody testing. Devices targeting inflammatory markers relevant for COVID-19 are also discussed, as fast, reliable bedside diagnostic tools for patient treatment and follow-up.
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Fundação para a Ciência e a Tecnologia
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SFRH/BD/115173/2016