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ChipCell

 ChipCell™  ­-  Small Flow Rate ApplicationsChipCell

 

 


The ChipCell is a specially designed reactor cell with very low volume (approx. 175 nL). It is ideal for small volume applications [1] and is typically used with flow rates in the range of 0.5 – 2.5 µL/min. The cell is made by a micromachining process, whereby a glass substrate is selectively etched to produce the desired channel structures.

The cell can be used in direct infusion mode with nano ESI/MS detection. Since the dead-volume free assembly assures the preservation of the chromatographic separation, the cell can also be used after a Capillary- or Nano LC separation to provide on-line CapillaryLC/Electrochemistry/ MS.

The chip is made of borosilicate glass with platinum (Pt) working, reference and counter electrodes. For optimal protection, the glass chip is delivered in a protective polymer cartridge of 75 x 25 mm, fully compatible with the ChipCell docking station.

 


ChipCell in protective polymer cartridge (black)

 

 

 

For easy handing the ChipCell is inserted into a stainless steel docking station containing ports for all fluidic and electric connections

 

 

 

ChipCell

 

Docking station inserted in black frame with all electric and fluidic connections. Fluidic connections are standard 1/16” PEEKSil tubing (25 or 100 µm ID). 

 

 

[1] developed in collaboration with Dr. M. Odijk, BIOS-group, MESA+, University of Twente, The Netherlands

 

 

Schematics ChipCell set-up with ChipCell assembly on top of ROXY Potentiostat: Direct infusion mode for detection by nano ESI/MS (A) and post-column separation mode, i.e., Nano LC/EC/MS mode (B), typical flow rates  0.5 to 2.5 uL/min.

 

 

 

 

The ChipCell is based on a 3 electrode thin-layer flow cell concept, with a “Y” shape, comprising of one inlet port and two outlet ports with separated working (WE) and counter electrode (CE) in each of the channel arms. The reference electrode is located in close proximity to the inlet. The smooth surface of the working electrode (WE) integrated in one of the channel arms results in virtually zero sample adsorption and carry over. The outlet of the WE channel is connected to the nano ESI/MS, meanwhile the outlet of the CE channel (opposite channel arm) is usually diverted to waste. The glass chip is designed as a disposable component and can be easily replaced once it gets irreversibly clogged or damaged.

Oxidative metabolism of Amodiaquine (m/z 355) with the two major metabolite m/z 326 and m/z 299 using the ChipCell, scan mode 0 - 2.0V; 20mV/s; flow rate through working electrode channel (WE) ca. 500 nL/min.

 

The ChipCell is used with the ROXY Potentiostat and for direct infusion mode it is supplied with the appropriate syringe pump. For additional details, see the description of the ROXY EC system. The flow rate and working potential can be optimized using the Dialogue software or dedicated MS software, e.g., XCalibur.


Product Flyers

 

Part no Description
205.0035 ChipCell kit, consisting of three ChipCells in protectivecartridges, ChipCell docking station + frame and electricalconnections to the ROXY Potentiostat
Not included is the 1/16” PEEKSIL connection kit, seeordering information below
205.0150 100 μm ID, 1/16” PEEKSIL connection kit, consisting of alltubing, nuts and ferrules for connecting to the dockingstation, recommended for infusion mode EC/MS
205.0152 25 μm ID, 1/16” PEEKSIL connection kit, consisting of alltubing, nuts and ferrules for connecting to the dockingstation, recommended for Capillary- or Nano LC/EC/MS
   
Spare Parts
205.0040
ChipCell docking station
205.0045 ChipCell with Pt electrodes, 1 pcs
250.0134 Cell cable for ChipCell


23020795 - Improved conversion rates in drug screening applications using miniaturized electrochemical cells with frit channels.
Odijk M, Olthuis W, van den Berg A, Qiao L, Girault H.; Anal Chem. 2012 Nov 6;84(21):9176-83. doi: 10.1021/ac301888g. Epub 2012 Oct 22.

25531627 - Mass Spectrometric Detection of Short-Lived Drug Metabolites Generated in an Electrochemical Microfluidic Chip
Floris T. G. van den Brink, Lars Bueter, Mathieu Odijk, Wouter Olthuis, Uwe Karst, and Albert van den Berg; Anal. Chem., 2015, 87 (3), pp 1527-1535