Multifunctional microfluidic chip for optical nanoprobe based RNA detection - Application to Chronic Myeloid Leukemia

Pedro Urbano Alves, Raquel Vinhas, Alexandra R. Fernandes, Semra Zuhal Birol, Levent Trabzon, Iwona Bernacka-Wojcik, Rui Igreja, Paulo Lopes, Pedro Viana Baptista*, Hugo Águas, Elvira Fortunato, Rodrigo Martins

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23 Atıf (Scopus)

Özet

Many diseases have their treatment options narrowed and end up being fatal if detected during later stages. As a consequence, point-of-care devices have an increasing importance for routine screening applications in the health sector due to their portability, fast analyses and decreased cost. For that purpose, a multifunctional chip was developed and tested using gold nanoprobes to perform RNA optical detection inside a microfluidic chip without the need of molecular amplification steps. As a proof-of-concept, this device was used for the rapid detection of chronic myeloid leukemia, a hemato-oncological disease that would benefit from early stage diagnostics and screening tests. The chip passively mixed target RNA from samples, gold nanoprobes and saline solution to infer a result from their final colorimetric properties. An optical fiber network was used to evaluate its transmitted spectra inside the chip. Trials provided accurate output results within 3 min, yielding signal-to-noise ratios up to 9 dB. When compared to actual state-of-art screening techniques of chronic myeloid leukemia, these results were, at microscale, at least 10 times faster than the reported detection methods for chronic myeloid leukemia. Concerning point-of-care applications, this work paves the way for other new and more complex versions of optical based genosensors.

Orijinal dilİngilizce
Makale numarası381
DergiScientific Reports
Hacim8
Basın numarası1
DOI'lar
Yayın durumuYayınlandı - 1 Ara 2018

Bibliyografik not

Publisher Copyright:
© 2017 The Author(s).

Finansman

This work was funded by FEDER funds through the COMPETE 2020 Programme and National Funds through FCT -Portuguese Foundation for Science and Technology under the project number POCI-01-0145-FEDER-007688, Reference UID/CTM/50025/2013, and project DISERTOX, Reference PTDC/CTM-NAN/2912/2014. This work was also supported by the Unidade de Ciências Biomoleculares Aplicadas – UCIBIO, financed by national funds from FCT/MCTES (UID/Multi/04378/2013) and co-financed by the ERDF under the PT2020 Partnership Agreement (POCI-01-0145-FEDER-007728); PD/BD/52211/2013 for RV. The authors would like to thank Daniela Gomes, Manuel Mendes and Andreia Araujo for the assistance with the sample preparation and scanning electron microscope images, and to Maryam Nasirpour for proofreading.

FinansörlerFinansör numarası
FCT/MCTES
Fundação para a Ciência e a TecnologiaPOCI-01-0145-FEDER-007688, UID/CTM/50025/2013, PTDC/CTM-NAN/2912/2014
Programa Operacional Temático Factores de Competitividade
Applied Molecular Biosciences Unit

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