Author
Listed:
- Guillaume Petit-Pierre
(Laboratory of Microsystems LMIS4, Ecole Polytechnique Fédérale de Lausanne (EPFL))
- Philippe Colin
(Brain Mind Institute, Ecole Polytechnique Fédérale de Lausanne (EPFL))
- Estelle Laurer
(Lausanne University Hospital, Geneva University Hospitals)
- Julien Déglon
(Lausanne University Hospital, Geneva University Hospitals)
- Arnaud Bertsch
(Laboratory of Microsystems LMIS4, Ecole Polytechnique Fédérale de Lausanne (EPFL))
- Aurélien Thomas
(Lausanne University Hospital, Geneva University Hospitals
University of Lausanne)
- Bernard L. Schneider
(Brain Mind Institute, Ecole Polytechnique Fédérale de Lausanne (EPFL))
- Philippe Renaud
(Laboratory of Microsystems LMIS4, Ecole Polytechnique Fédérale de Lausanne (EPFL))
Abstract
Direct collection of extracellular fluid (ECF) plays a central role in the monitoring of neurological disorders. Current approaches using microdialysis catheters are however drastically limited in term of temporal resolution. Here we show a functional in vivo validation of a droplet collection system included at the tip of a neural probe. The system comprises an advanced droplet formation mechanism which enables the collection of neurochemicals present in the brain ECF at high-temporal resolution. The probe was implanted in a rat brain and could successfully collect fluid samples organized in a train of droplets. A microfabricated target plate compatible with most of the surface-based detection methods was specifically developed for sample analysis. The time-resolved brain-fluid samples are analyzed using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The results provide a time evolution picture of the cerebral tissues neurochemical composition for selected elements known for their involvement in neurodegenerative diseases.
Suggested Citation
Guillaume Petit-Pierre & Philippe Colin & Estelle Laurer & Julien Déglon & Arnaud Bertsch & Aurélien Thomas & Bernard L. Schneider & Philippe Renaud, 2017.
"In vivo neurochemical measurements in cerebral tissues using a droplet-based monitoring system,"
Nature Communications, Nature, vol. 8(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-01419-1
DOI: 10.1038/s41467-017-01419-1
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