Page 234 - Advances in Forensic Applications of Mass Spectrometry - Jehuda Yinon
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                             coupling of gas chromatography with mass ion isolation with the first mass
                             spectrometer, followed by a second MS stage of dissociation through ion
                             collisions and subsequent detection of the daughter ions formed. The second
                             dissociation and new daughter ion spectrum detected by the second MS
                             operation creates the added specificity that labels GC/MS/MS as perhaps the
                             ultimate method today for mixture analysis.
                                In MS/MS, a significant ion from a targeted compound or a characteristic
                             ion from a chemical class is chosen from a full scan GC/MS mass spectrum.
                             This is the parent (or precursor) ion. In the MS/MS acquisition, the chosen
                             parent ion is isolated in the first MS operation. In the second MS stage it
                             undergoes collision induced dissociation (CID) with helium reagent gas, which
                             results in a new daughter ion (or product ion) spectrum. The isolation and
                             CID process makes MS/MS inherently more selective than MS alone, and this
                             presents numerous advantages for complex samples where analyte and matrix
                             coelution are common. An ion trap mass spectrometer that includes tandem
                             mass spectrometry in time also offers advantages of reduced electronics, man-
                             ifolds, and pumps (and price), compared to a triple linear quadrupole mass
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                             spectrometer which is based on tandem mass spectrometry in space.  The latest
                             ion trap mass spectrometers include higher scan rates, external ionization, and
                             the capability of obtaining both full scan and MS/MS information in the same
                             analytical run. This use of GC/MS/MS is not new. This tandem mass spec-
                             trometry approach has clearly been shown to be the method of choice for
                             biological specimens, detection of explosives, and drugs of abuse, as well as
                             for structure elucidation in pharmaceutical analysis. Its application in forensic
                             laboratories has been limited in the past by the cost and complexity of the
                             instrumentation. This has changed with the relatively low cost and high effi-
                             ciency of conducting MS/MS in an ion trap mass spectrometer.
                                GC/MS/MS has been used to address problems of analytes in complex
                             matrices such as THC in blood,  trace quantities in difficult matrices such
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                             as residues of drugs of abuse in hair,  or to minimize the matrix interferences
                                                            7
                             in the analysis of pesticides in fruits and vegetables. 8
                                The high sensitivity and selectivity of GC/MS/MS have been used in the
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                             detection of trace components in explosive mixtures.  These are important
                             in environmental remediation projects or for high-speed security sweeps such
                             as those done at airports.
                                GC/MS/MS is one of the laboratory’s “big guns” used when the result
                             must have the highest defensibility.  An example is the use of MS/MS
                             (although with liquid chromatographic separation) in the much publicized
                             O.J. Simpson trial. A method using LC/MS/MS was developed to determine
                             whether the blood stained cloth swatch and socks found at the O.J. Simpson
                             residence contained the blood preservative EDTA. The analysis successfully
                             determined that EDTA was not present in the evidence at levels indicating


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