Multiple reaction mode

The method for chloroacetanilide soil metabolites in water determines concentrations of ethanesulfonic acid (ESA) and oxanilic acid (OXA) metabolites of alachlor, acetochlor, and metolachlor in surface water and groundwater samples by direct aqueous injection LC/MS/MS. After injection, compounds are separated by reversed-phase HPLC and introduced into the mass spectrometer with a TurboIonSpray atmospheric pressure ionization (API) interface. Using direct aqueous injection without prior SPE and/or concentration minimizes losses and greatly simplifies the analytical procedure. Standard addition experiments can be used to check for matrix effects. With multiple-reaction monitoring in the negative electrospray ionization mode, LC/MS/MS provides superior specificity and sensitivity compared with conventional liquid chromatography/mass spectrometry (LC/MS) or liquid chromatography/ultraviolet detection (LC/UV), and the need for a confirmatory method is eliminated. In summary,... 

LC/MS/MS. LC/MS/MS is used for separation and quantitation of the metabolites. Using multiple reaction monitoring (MRM) in the negative ion electrospray ionization (ESI) mode, LC/MS/MS gives superior specificity and sensitivity to conventional liquid chromatography/mass spectrometry (LC/MS) techniques. The improved specificity eliminates interferences typically found in LC/MS or liquid chro-matography/ultraviolet (LC/UV) analyses. Data acquisition is accomplished with a data system that provides complete instmment control of the mass spectrometer. 

Electrospray (Turbo lonSpray), negative ion mode MS/MS with multiple reaction monitoring (MRM) -4500 V... 

The LC-MS/MS technique has been used to quantify and identify phenolic compounds. In order to quantify, multiple reaction monitoring (MRM), in which there is a combination of the precursor ion and one of its daughter fragments, is used to characterize a particular compound. This behavior should be as specific as possible in samples with a complex mixture of phenolic compounds. This technique has been largely used to quantify phenolic compound metabolites in urine and plasma (Urpf-Sarda and others 2005, 2007). In this context, LC-ESI-MS/MS with negative mode has been applied for the identification of a variety of phenolic compounds in a cocoa sample (Sanchez-Rabaneda and others 2003 Andres-Lacucva and others 2000). 

The multiple reaction monitoring (MRM) conditions for each analyte were optimized by infusing 0.1 jxglmL of analyte in mobile phase. The Ionspray needle was maintained at 4.0 kV and the turbo gas temperature was 650°C. Nebulizing gas, auxiliary gas, curtain gas, and collision gas flows were set at 35, 35,40, and 4, respectively. In the MRM mode, collision energies of 17,16, and 15 eV... 

Skutlarek D, Faerber H, lippert F, Ulbrich A, Wawrzun A, Buening-Pfaue H (2004) Determination of glucosinolate profiles in Chinese vegetables by precursor ion scan and multiple reaction monitoring scan mode (LC-MS/MS). Eur Food Res Technol 219 643-649... 

GC/MS(/MS) is also popular for quantifying DBFs. Selected ion monitoring (SIM) or multiple reaction monitoring (MRM) mode are used with GC/MS and GC/ MS/MS, respectively, to maximize the sensitivity and provide low detection limits. Some EFA Methods utilize GC/MS, including EFA Method 524.2, which uses GC/ EI-MS for THM analysis [155], and EFA Method 521, which uses for GC/CI-MS/ MS for nitrosamine analysis [55]. In addition, many priority unregulated DBFs have been measured using GC/MS in a U.S. Nationwide Occurrence Study [11,12]. 

Based on an in-vial derivatization method, the mass spectra of methylated flavonoids and other phenolics have been obtained via EI-MS at 70 eV. Detection was performed in the selective ion monitoring mode and peaks were identified and quantified using target ions. The detection limits ranged between 2 and 40 ng/ml, whereas the limits of quantitation fall in the range of 5 to 118 ng/ml, with flavonoids accounting for the lowest sensitivity due to their multiple reaction behavior. 

Homocarnosine is a dipeptide of GABA and L-histidine. After deproteinizing the sample with ethanol, the mixtures are centrifuged. The clear supernatant is evaporated to dryness and derivatized with butanol. The sample is evaporated to dryness and redissolved in the mobile phase. The homocarnosine-butyl derivatives (Fig. 2.3.4) are quantified using liquid chromatography mass spectrometry/mass spectrometry (LC-MS/MS) operating in the positive mode. With multiple reaction monitoring (MRM), the transitions of m/z 297.0 to m/z 212.0 for homocarnosine and m/z 299.0 to m/z 212.0 for 2H2-L-homocarnosine are quantified. 

Following the extractive deproteinization of the plasma, urine, or CSF, PA is de-rivatized with methyl chloroformate. The analyte is measured in the tandem mass spectrometer in the positive ion mode using multiple reaction monitoring (MRM Fig. 2.4.2). 

Formiminoglutamate (FIGLU), a marker for glutamate formimino-transferase deficiency, was recently also shown to be detectable by acylcarnitine analysis represented as a peak with m/z 287 (Fig. 3.2.3d) [64]. In poorly resolved acylcarnitine profiles, this peak may be confused with iso-/butyrylcarnitine (m/z 288). To avoid the incorrect interpretation of acylcarnitine profiles, we recommend performing the analysis in product scan mode as opposed to multiple reaction monitoring (MRM) mode. For example, the FIGLU peak at m/z 287 would not have been correctly identified in MRM mode because the transition of 287 to 85 is typically not selected. However, the 288/85 transition would reveal abnormal results, but in fact not represent either butyryl- or isobutyrylcarnitine, but another FIGLU related ion species. 

Coupling of liquid chromatography with mass spectrometry can provide unequivocal on-line spectrometric identification of anthelminthic residues in animal-derived foods. Typical applications of such techniques include the confirmation of moxidectin residues in cattle fat by liquid chromatography-thermospray mass spectrometry (352), and the confirmation of eprinomectin residues in bovine liver tissue by liquid chromatography, electrospray ionization, and multiple reaction monitoring in the MS-MS mode with positive ion detection (370). 

Several scan modes are unique to the triple-quadrupole instrument, and most of these modes are superior in duty cycle versus an ion trap, Fourier transform (FT), or time-of-flight (TOF) mass spectrometers. Different elements of the triple-quadrupole perform different operations for each scan mode. These scan modes, each of which will be described in detail, are single-reaction monitoring (SRM) or multiple-reaction monitoring (MRM), precursor ion scanning (PIS), and constant-neutral-loss scanning (NLS). These scan modes and applications for structural elucidation have been described in detail (Yost and Enke, 1978, 1979). 

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