6 research outputs found
Ambient Mass Spectrometry Imaging: Plasma Assisted Laser Desorption Ionization Mass Spectrometry Imaging and Its Applications
Mass spectrometry imaging (MSI) has been widely used in many research areas for the advantages of providing informative molecular distribution with high specificity. Among the recent progress, ambient MSI has attracted increasing interests owing to its characteristics of ambient, in situ, and nonpretreatment analysis. Here, we are presenting the ambient MSI for traditional Chinese medicines (TCMs) and authentication of work of art and documents using plasma assisted laser desorption ionization mass spectrometry (PALDI-MS). Compared with current ambient MSI methods, an excellent average resolution of 60 mu m x 60 mu m pixel size was achieved using this system. The feasibility of PALDI-based MSI was confirmed by seal imaging, and its authentication applications were demonstrated by imaging of printed Chinese characters. Imaging of the Radix Scutellariae slice showed that the two active components, baicalein and wogonin, mainly were distributed in the epidermis of the root, which proposed an approach for distinguishing TCMs' origins and the distribution of active components of TCMs and exploring the environmental effects of plant growth. PALDI-MS imaging provides a strong complement for the MSI strategy with the enhanced spatial resolution, which is promising in many research fields, such as artwork identification, TCMs' and botanic research, pharmaceutical applications, etc
Ambient Mass Spectrometry Imaging: Plasma Assisted Laser Desorption Ionization Mass Spectrometry Imaging and Its Applications
Mass
spectrometry imaging (MSI) has been widely used in many research
areas for the advantages of providing informative molecular distribution
with high specificity. Among the recent progress, ambient MSI has
attracted increasing interests owing to its characteristics of ambient,
in situ, and nonpretreatment analysis. Here, we are presenting the
ambient MSI for traditional Chinese medicines (TCMs) and authentication
of work of art and documents using plasma assisted laser desorption
ionization mass spectrometry (PALDI-MS). Compared with current ambient
MSI methods, an excellent average resolution of 60 μm ×
60 μm pixel size was achieved using this system. The feasibility
of PALDI-based MSI was confirmed by seal imaging, and its authentication
applications were demonstrated by imaging of printed Chinese characters.
Imaging of the <i>Radix Scutellariae</i> slice showed that
the two active components, baicalein and wogonin, mainly were distributed
in the epidermis of the root, which proposed an approach for distinguishing
TCMs’ origins and the distribution of active components of
TCMs and exploring the environmental effects of plant growth. PALDI-MS imaging provides
a strong complement for the MSI strategy with the enhanced spatial
resolution, which is promising in many research fields, such as artwork
identification, TCMs’ and botanic research, pharmaceutical
applications, etc
Rapid In Situ Profiling of Lipid Cî—»C Location Isomers in Tissue Using Ambient Mass Spectrometry with Photochemical Reactions
Rapid
and in situ profiling of lipids using ambient mass spectrometry
(AMS) techniques has great potential for clinical diagnosis, biological
studies, and biomarker discovery. In this study, the online photochemical
reaction involving carbon–carbon double bonds was coupled with
a surface sampling technique to develop a direct tissue-analysis method
with specificity to lipid Cî—»C isomers. This method enabled
the in situ analysis of lipids from the surface of various tissues
or tissue sections, which allowed the structural characterization
of lipid isomers within 2 min. Under optimized reaction conditions,
we have established a method for the relative quantitation of lipid
Cî—»C location isomers by comparing the abundances of the diagnostic
ions arising from each isomer, which has been proven effective through
the established linear relationship (<i>R</i><sup>2</sup> = 0.999) between molar ratio and diagnostic ion ratio of the FA
18:1 Cî—»C location isomers. This method was then used for the
rapid profiling of unsaturated lipid Cî—»C isomers in the sections
of rat brain, lung, liver, spleen, and kidney, as well as in normal
and diseased rat tissues. Quantitative information on FA 18:1 and
PC 16:0–18:1 CC isomers was obtained, and significant
differences were observed between different samples. To the best of
our knowledge, this is the first study to report the direct analysis
of lipid Cî—»C isomers in tissues using AMS. Our results demonstrated
that this method can serve as a rapid analytical approach for the
profiling of unsaturated lipid Cî—»C isomers in biological tissues
and should contribute to functional lipidomics and clinical diagnosis
Pulsed Direct Current Electrospray: Enabling Systematic Analysis of Small Volume Sample by Boosting Sample Economy
We had developed pulsed direct current
electrospray ionization
mass spectrometry (pulsed-dc-ESI-MS) for systematically profiling
and determining components in small volume sample. Pulsed-dc-ESI utilized
constant high voltage to induce the generation of single polarity
pulsed electrospray remotely. This method had significantly boosted
the sample economy, so as to obtain several minutes MS signal duration
from merely picoliter volume sample. The elongated MS signal duration
enable us to collect abundant MS<sup>2</sup> information on interested
components in a small volume sample for systematical analysis. This
method had been successfully applied for single cell metabolomics
analysis. We had obtained 2-D profile of metabolites (including exact
mass and MS<sup>2</sup> data) from single plant and mammalian cell,
concerning 1034 components and 656 components for <i>Allium cepa</i> and HeLa cells, respectively. Further identification had found 162
compounds and 28 different modification groups of 141 saccharides
in a single <i>Allium cepa</i> cell, indicating pulsed-dc-ESI
a powerful tool for small volume sample systematical analysis