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Real-time selective detection of dopamine and serotonin at nanomolar concentration from complex in vitro systems

  • Samuel Rantataro*
  • , Ilmari Parkkinen
  • , Mikko Airavaara
  • , Tomi Laurila*
  • *Tämän työn vastaava kirjoittaja
  • University of Helsinki

Tutkimustuotos: LehtiartikkeliArticleScientificvertaisarvioitu

42 Sitaatiot (Scopus)
121 Lataukset (Pure)

Abstrakti

Electrochemical sensors provide means for real-time monitoring of neurotransmitter release events, which is a relatively easy process in simple electrolytes. However, this does not apply to in vitro environments. In cell culture media, competitively adsorbing molecules are present at concentrations up to 350 000-fold excess compared to the neurotransmitter-of-interest. Because detection of dopamine and serotonin requires direct adsorption of the analyte to electrode surface, a significant loss of sensitivity occurs when recording is performed in the in vitro environment. Despite these challenges, our single-walled carbon nanotube (SWCNT) sensor was capable of selectively measuring dopamine and serotonin from cell culture medium at nanomolar concentration in real-time. A primary midbrain culture was used to prove excellent biocompatibility of our SWCNT electrodes, which is a necessity for brain-on-a-chip models. Most importantly, our sensor was able to electrochemically record spontaneous transient activity from dopaminergic cell culture without altering the culture conditions, which has not been possible earlier. Drug discovery and development requires high-throughput screening of in vitro models, being hindered by the challenges in non-invasive characterization of complex neuronal models such as organoids. Our neurotransmitter sensors could be used for real-time monitoring of complex neuronal models, providing an alternative tool for their characterization non-invasively.

AlkuperäiskieliEnglanti
Artikkeli115579
JulkaisuBiosensors and Bioelectronics
Vuosikerta241
DOI - pysyväislinkit
TilaJulkaistu - 1 jouluk. 2023
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Rahoitus

We wish to thank Canatu Oy, Finland, for kindly providing us the SWCNT network samples, and PhD Toni Pasanen for kindly providing us the antireflective black silicon material that was used in upright fluorescence imaging. We acknowledge the provision of facilities by Aalto University at OtaNano - Micronova Nanofabrication Centre and we would also like to thank the Biomedicum Imaging Unit (BIU), Helsinki, for microscopy services. This work was supported by European Union's Horizon 2020 research and innovation programme H2020-FETPROACT-2018-01 (No. 824070), Doctoral Progamme in Drug Research (University of Helsinki), and Sigrid Juselius Foundation. We wish to thank Canatu Oy, Finland, for kindly providing us the SWCNT network samples, and PhD Toni Pasanen for kindly providing us the antireflective black silicon material that was used in upright fluorescence imaging. We acknowledge the provision of facilities by Aalto University at OtaNano - Micronova Nanofabrication Centre and we would also like to thank the Biomedicum Imaging Unit (BIU), Helsinki, for microscopy services. This work was supported by European Union's Horizon 2020 research and innovation programme H2020-FETPROACT-2018-01 (No. 824070 ), Doctoral Progamme in Drug Research (University of Helsinki) , and Sigrid Juselius Foundation .

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