Quadrupole mass spectrometer,triple quantitative analysis

Multiple reaction monitoring (MRM) MRM is the most common mode of using a triple quadrupole mass spectrometer for quantitative analysis,... 

For HPLC/MS/MS analysis, a triple-quadrupole mass spectrometer with an electrospray interface is recommended for achieving the best sensitivity and speciflcity in the quantitative determination of oxime carbamates and their metabolites. This allows... 

The results thus show that ammonia DCI-MS/MS using a triple quadrupole mass spectrometer is a convenient method for the detection of additives in PE samples. The softness and selectivity provided by ammonia DCI in combination with the specificity provided by CID, demonstrate great potential for identification of additives directly from PE extracts. The utility of DCI in the quantitative analysis of additives has still to be explored. DCI-MS/MS (B/E) with high collision... 

Quadrupole mass spectrometers [10] or quadrupole ion traps are today the most widely used mass spectrometers. The physical bases were described in the early 1950s by Paul and Steinwedel. For his work Paul received the Nobel Prize in 1989 [11]. Triple quadrupole mass spectrometers have become very popular instruments for qualitative and quantitative analysis. Yost et al. [12] built in 1978 the first instrument and it took four years before this type of instrument was commercialized. The coupling with liquid chromatography or gas chromatography is well established and benchtop ion traps or quadrupoles are nowadays part of the standard equipment of many analytical laboratories. 

Another recent innovation is the QTrap mass spectrometer. The QTrap MS system combines the capabilities of a triple quadrupole mass spectrometer and a linear ion trap mass spectrometer into one MS system. Initially, the QTrap MS was used primarily as a tool for metabolite identification studies [34, 35, 38]. As reported by Li et al. [138], the QTrap MS can also be used as an excellent system for the quantitative analysis of discovery PK samples. The advantage of the QTrap MS system for quantitative analysis is that it can be used to look for plasma metabolites of the NCE and provide an easy way to monitor them while providing the quantitative data on the NCE. 

Smith, C.J., Wilson, I.D., Abou-Shakra, F., Payne, R., Parry, T.C., Sinclair, P., Roberts, D. W. A comparison of the quantitative methods for the analysis of the platinum-containing anticancer drug cii-amminedichloro(2-methylpyridine)]-platinum(II) (ZD0473) by HPLC coupled to either a triple quadrupole mass spectrometer or an inductively coupled plasma mass spectrometer. Anal. Chem. 75, 1463-1469 (2003)... 

A triple-quadrupole linear ion trap (QqLIT), which is the most widely used hybrid linear ion trap, is based on the ion path of a triple-quadrupole mass spectrometer with Q3 operated as either a conventional RF/DC quadrupole mass filter or a linear ion trap mass spectrometer. " A QqLIT combines the advantages of a QqQ and a QIT within the same platform without compromising the performance of either mass spectrometer. It retains classical QqQ functions such as MRM, product ion scan, precursor ion scan, and constant neutral loss scan for quantitative and qualitative analysis, and possesses MS" ion accumulation... 

Figure 13.7 Setup for mass specirrmietry-based quantitative real-time analysis. The outlet flow of a cwtinuous stirred enzyme membrane reactor (EMR) is continuously analyzed by multiple reaction monitoring in an electrospray ionization triple quadrupole mass spectrometer after flow reduction (SI), dilution (T) and another flow reduction (S2) (S6j. Reprinted by permission from Macmillan Publishers Ltd Nature Chemical Biology [Bujara, M., SchumperU, M., Pellaux, R., Heinemann, M., Panke, S. (2011) Optimization of a Blueprint f

Optimization In MRM-based quantitative analysis using triple quadrupole mass spectrometers, a unique transition for each compound is first selected to ensure high specificity and low background noise. The corresponding ion optics parameters for the particular SRM transition, such as source lens voltage and collision energy, are then optimized to achieve the best sensitivity. 

As mentioned in the previous section, triple-quadrupole instruments are very good at finding low levels and structurally related compounds in the presence of biological matrices as well as being the gold standard technique for quantitation. Ion trap mass spectrometers, on the other hand, have the capabilities to obtain high-sensitivity full-scan MS and MS/MS spectra therefore, they are widely used for qualitative analysis, such as structural elucidation and unknown identification. For complete metabolite identification, it is important to have both the sensitivity and selectivity of triple-quadrupole instruments and the full-scan data quality of ion traps. 

Superior sensitivity, efficiency, and specificity have made high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS), the predominant analytical technique for characterization and quantitative analysis of metabolites (Kostiainen et al., 2003 Ma et al., 2006 Prakash et al., 2007). Ion trap, triple-quadrupole, and quadmpole time-of-flight (Q-TOF) mass spectrometers are routinely used to profile and characterize metabolites in plasma and excreta (Ma et al., 2006). The combination of scan types and features available on mass spectrometers of different design (product ion, MS", neutral loss, precursor ion scans, accurate mass measurements) allows identification and characterization of putative and unexpected metabolites with or without little prior knowledge of biotransformation pathways of a given dmg molecule. 

For the detection, a tandem mass spectrometer Quattro Micro API ESCI (Waters Corp., Milford, MA) with a triple quadrupole was employed. The instrument was operated in electrospray in the positive ionization mode (ESI+) with the following optimized parameters capillary voltage, 0.5 kV source block temperature, 130 °C nebulization and desolvation gas (nitrogen) heated at 400 °C and delivered at 800 L/h, and as cone gas at 50 L/h collision cell pressure, 3 x 1(F6 bar (argon). Data was recorded in the multiple reaction monitoring (MRM) mode by selection of the two most intense precursor-to-product ion transitions for each analyte, except for the ISs, for which only one transition was monitored. The most intense transition for each analyte was used for quantitative purposes. Table 2 shows MRM transitions, cone voltages and collision energies used for the analysis of the antidepressants included in the LC-MS/MS method. 

In addition, due to lack of MS/MS capability, SIM has been more commonly performed on single quadrupole MS, while SRM has been broadly adapted on triple quadrupole (Figure 13-4) and ion-trap mass spectrometers. The increase in sensitivity and selectivity of SRM stem from the ion-chromatogram (i.e., LC-MS/MS) obtained by specific precursor-to-product ion transition for an analyte of interest (Figure 13-4). Conversely, in an SIM mode, the relative background noise due to the presence of other isobaric species (i.e., ions with a same m/z as the analyte of interest) can result in a lower signal-to-noise ratio for the analyte. Due to the widespread acceptance of SRM in quantitative analysis, the remaining part of this section focuses on a description of tandem-mass spectrometry (MS/MS), which is utilized in SRM (or MRM) experiments. 

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