AI Article Synopsis

  • Glass microfluidic chips are advantageous for mass spectrometry due to their design and resistance to chemicals, but creating a nanospray ionization emitter in glass is challenging.
  • A new method using continuous fluid-assisted etching has been developed to produce sharp 3D nESI emitters within the chips, allowing for efficient integration.
  • The system successfully detects neurochemicals in tiny droplets and shows promise for future applications in neurochemical monitoring and single-cell analysis.

Article Abstract

Glass microfluidic chips are suitable for coupling with mass spectrometry (MS) due to their flexible design, optical transparency and resistance to organic reagents. However, due to the high hardness and brittleness of glass, there is a lack of simple and feasible technology to manufacture a monolithic nanospray ionization (nESI) emitter on a glass microchip, which hinders its coupling with mass spectrometry. Here, a continuous fluid-assisted etching strategy is proposed to fabricate monolithic three-dimensional (3D) nESI emitters integrated into glass microchips. A continuous fluid of methanol is adopted to protect the inner wall of the channels and the bonding interface of the glass microfluidic chip from being wet-etched, forming sharp 3D nESI emitters. The fabricated 3D nESI emitter can form a stable electrospray plume, resulting in consistent nESI detection of acetylcholine with an RSD of 4.5% within 10 min. The fabricated 3D emitter is integrated on a glass microfluidic chip designed with a T-junction droplet generator, which can realize efficient analysis of acetylcholine in picoliter-volume droplets by nESI-MS. Stability testing of over 20 000 droplets detected by the established system resulted in an RSD of 9.1% over approximately 180 min. The detection of ten neurochemicals in rat cerebrospinal fluid droplets is achieved. The established glass droplet microfluidic chip-MS system exhibits potential for broad applications such as neurochemical monitoring and single-cell analysis in the future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11110156PMC
http://dx.doi.org/10.1039/d4sc01700eDOI Listing

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