Publications by authors named "Christopher Kenji Brenden"

Article Synopsis
  • Microdialysis (MD) is a key method used to analyze chemicals in biological tissues, useful in various fields like neurology and dermatology, but it faces limitations in sensitivity and resolution.
  • The development of a nanodialysis (ND) probe using advanced silicon microfabrication offers improved chemical sampling, achieving 100 μm spatial resolution and subsecond timing, significantly outperforming traditional MD techniques.
  • These ND probes can provide detailed, minimally invasive sampling in live tissues, opening up opportunities for advancements in clinical and pharmaceutical research.
View Article and Find Full Text PDF

Microdialysis (MD) is a versatile and powerful technique for chemical profiling of biological tissues and is widely used for quantification of neurotransmitters, neuropeptides, metabolites, biomarkers, and drugs in the central nervous system as well as in dermatology, ophthalmology, and in pain research. However, MD performance is severely limited by fundamental tradeoffs between chemical sensitivity, spatial resolution, and temporal response. Here, by using wafer-scale silicon microfabrication, we develop and demonstrate a nanodialysis (ND) sampling probe that enables highly localized chemical sampling with 100μm spatial resolution and sub-second temporal resolution at high recovery rates.

View Article and Find Full Text PDF

Implantable electrochemical sensors enable fast and sensitive detection of analytes in biological tissue, but are hampered by bio-foulant attack and are unable to be recalibrated in-situ. Herein, an electrochemical sensor integrated into ultra-low flow (nL/min) silicon microfluidic channels for protection from foulants and in-situ calibration is demonstrated. The small footprint (5 μm radius channel cross-section) of the device allows its integration into implantable sampling probes for monitoring chemical concentrations in biological tissues.

View Article and Find Full Text PDF

A silicon single-chip microfluidics system that integrates microscale fluidic channels, an analyte segmentation device, and a nozzle for electrohydrodynamic-assisted printing is designed for hyphenation with MALDI mass spectrometry (MS) imaging. A miniaturized T-junction segments analytes into monodisperse picoliter oil-isolated compartments. The printing nozzle deposits generated droplets one-by-one into an array on a conductive substrate without splitting or coalescing.

View Article and Find Full Text PDF