LCGC Europe Application Note Alert
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November 2015
 

Sample Prep
The Analysis of Chlorinated Dioxins, Difurans, and Polychlorinated Biphenyls in Edible Oils
The dioxin family consists of 210 compounds, of which 17 contain the 2,3,7,8 pattern of chlorination. These 2,3,7,8-containing compounds are of extreme concern to human health because of their high level of toxicity. Approximately, 12 of the 209 polychlorinated biphenyls have also been identified as human toxins. For this reason, the US FDA and EU have established strict regulations for the monitoring of food products for human consumption, in particular edible oils. Manual extractions of oils can be a time-consuming procedure often delaying lab turnaround times. By automating the process with the PowerPrep®, food oil samples can be reliably processed with routine 24 h turnaround times.
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Determination of 35 Pesticides and Three Cannabinoids in Marijuana Edibles
As of July 2015 within the US, 23 states and Washington D.C. have legalized the medical use of marijuana, while 4 states and Washington D.C. have legalized the recreational use of marijuana. As a result, many forensic toxicology laboratories are looking for fast, reliable, and cost-effective methods to determine cannabis potency and pesticides in edibles. This application utilizes the advantages of QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) to extract 35 pesticides and three cannabinoids including tetrahydrocannabinol (THC), cannabidiol (CBD), and cannabinol (CBN) in edibles, followed by either serial dilutions for cannabis potency analysis, or a dispersive solid-phase extraction (dSPE) cleanup for pesticide residue analysis. This hybrid method allows the QuEChERs technique, which is extensively used in the food testing industry, to be utilized in a forensic setting.
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Extraction of Opioid Derivatives Using Evolute Express CX
This application note describes an extraction method for buprenorphine and norbuprenorphine from oral fluid using Evolute Express CX prior to LC–MS–MS analysis. Evolute Express products combine powerful “Evolute” sorbent chemistry with enhanced “Express” components. There is no need for conditioning and equilibration; just simply load, wash, and elute.
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HPLC
Separation of Free Amino Acids and Primary Amines Using Daicel Crown Ether Columns
A new generation of Daicel Crownpak chiral selectors, Crownpak CR-I(+) and Crownpak CR-I(-), can be used for the separation of free amino acids and primary amines. Recent scientific studies have demonstrated that the brains of Alzheimer’s disease patients contain unusually high levels of D-serine. This note describes the use of Crownpak CR-I(+) to develop the separation of DL-serine.
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Impurity Testing of Fixed-Dose Combination Drugs in UHPLC
This application note demonstrates that one injection is adequate to reliably quantify fixed-dose combination drugs using the Agilent 1290 Infinity II HDR-DAD Impurity Analyzer Solution.
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GPC
Absolute Molar Mass in UHPLC via the µDAWN and UT-rEX
Ultrahigh-performance liquid chromatography (UHPLC) enables fast, efficient separation of biomolecular samples. Compared to standard SEC, UHPLC–SEC provides improved resolution, higher throughput, less solvent, and smaller sample consumption for analysis of precious biological samples.
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GC
Rapidly Analyze a Wide Range of Glycol Ethers by GC–MS
Chromatographic conditions were developed for a fast GC–MS glycol ether analysis on the Rxi-1301Sil MS column. This cyano-based thin film column provides better resolution and faster run times than the thick film cyanopropylphenyl-type columns commonly used for speciation of the glycol ethers.
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What's in Your Morning Drink? Comprehensive Characterization of Coffee and Tea by GC×GC–TOF-MS
In this poster, from RAFA 2015, GC×GC–TOF-MS was used to identify a range of minor constituents in tea and coffee samples that may have escaped notice on a conventional GC–MS system as as a result of numerous co-elutions with higher-loading peaks. The excellent spectral quality provided confident identification of both targets and unknowns, even at trace levels, in a single run.
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GPC
Mass-Directed Isolation of a Synthetic Peptide Using the ACQUITY QDa Detector
This application note illustrates a simple mass-directed approach to peptide isolation and discusses the options for improving the efficiency of the purification protocol.
  •   Isolation is easily accomplished using the ACQUITY QDa Mass Detector as configured in the Waters AutoPurification System, making it a lower cost alternative for purification of those peptides with mono-isotopic masses or multiple charges that fall within the 30–1250 Da mass range of the detector.
  •   Columns with different selectivity are sometimes necessary for improving the separation of crude sample mixtures, which ultimately leads to the isolation of higher purity target peptides.
  •   Focusing the gradient improves the resolution of closely-eluting or co-eluting peptide impurities, contributing to the ease of target peptide isolation.
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