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Analytica 2016
September 28-30, 2016
Volume 7, Issue 5(Suppl)
J Anal Bioanal Tech 2016
ISSN: 2155-9872 JABT, an open access journal
conferenceseries
.com
September 28-30, 2016 Orlando, USA
7
th
International Conference and Exhibition on
Analytical & Bioanalytical Techniques
Huanwen Chen, J Anal Bioanal Tech 2016, 7:5(Suppl)
http://dx.doi.org/10.4172/2155-9872.C1.024Extractive electrospray ionization mass spectrometry for biosample analysis
Huanwen Chen
Jiangxi Key Laboratory for Mass Spectrometry and Instrumentation, China
M
ass spectrometry (MS) is one of the preferable analytical techniques for sensitive characterization of biological samples
on the molecular levels. Technological innovations advance mass spectrometry for sophisticate applications in many
fields including but not limited to chemistry, material sciences and life sciences. For trace analysis of a typical biological sample,
classical MS techniques require multi-step sample pre-treatment (e.g., grinding, extraction, separation, pre-concentration, etc.)
to obtain molecular information from the native biological samples, especially for detection of trace analytes distributed in the
3-dimensional volume of a bulk sample. Commonly associated with sample pre-treatment are biological degradation, chemical
reactions, reagent contamination, and material losses. Apparently, tedious sample pretreatments strangle the breakthrough of
high throughput in analytical mass spectrometry. By isolating the high electric filed required for ionization from any biological
sample, extractive electrospray ionization (EESI) allows direct detection of small metabolites and/or large proteins distributed
either on surfaces or inside bulk tissue by mass spectrometry, without any sample pretreatment. Experiments demonstrated that
EESI-MS minimizes matrix effects during the ionization process, enabling real-time,
in vivo
analysis of biofluids, biosurfaces,
aerosols and living objectives. Therein, the fundamental principle, instrumentation and typical applications of EESI-MS for
biological analysis can be summarized, giving emphases on progresses in our lab for sensitive qualitative/quantitative detection
of chemicals located inside a bulk tissue of whole-volume (≥20 mm
3
), with neither mashing/grinding the sample nor matrixes
clean-up. Furthermore, the emerging utilization of EESI-MS for sequentially acquiring metabolites, lipids, and proteins in a
single tissue sample will be presented for the first time.
Biography
Huanwen Chen has completed his PhD from Jilin University and Postdoctoral studies from Aston Lab, Purdue University. He is the Director of Jiangxi Key
Laboratory for Mass Spectrometry and Instrumentation. He has published more than 200 papers in reputed journals and has been serving as an Editorial Board
Member of repute.
chw8868@gmail.com