Thermo Fisher Scientific’s FAIMS-based LC/MS Analytical Method is Validated by A&M Labor fuer Analytik to Ensure Human Safety in Drug Development

3 Dec 2007
Greg Smith
Analyst / Analytical Chemist

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Thermo Fisher Scientific Inc., the world leader in serving science, today announced that researchers in Germany’s A&M Labs have validated a method that uses innovative Thermo Scientific high-Field Asymmetric waveform Ion Mobility Spectrometry (FAIMS) technology to remove interferences from a drug analysis. Using this method, the researchers can adhere to the guidelines of the FDA to ensure human safety in drug development. Unforeseen analyte interferences can cause validated LC-MS methods to fail, resulting in costly delays in obtaining data from clinical trials. Another impact of co-eluting interferences is data misinterpretation, which could cause dosing errors in human test subjects. The method was presented to the scientific community at the annual LC/MS workshop in Wuppertal, Germany on November 13, 2007.

Dr. Axel Roemer, research leader at A&M, presented the findings. “We were very impressed with how the Thermo Scientific FAIMS system allows us to remove interferences with our drug analysis method,” said Dr. Roemer. “Keeping at the forefront of science is important for us to bring new therapies to patients.”

The FAIMS interface for the Thermo Scientific TSQ Quantum™ series of mass spectrometers works in combination with the H-ESI and APCI ion probes at atmospheric pressure to increase selectivity during analysis. FAIMS provides additional ion filtering, resulting in LC-MS/MS chromatograms with reduced chemical background and endogenous interferences.

“We are pleased that Dr. Roemer and his team at A&M Labs could develop a validated LC-MS assay using FAIMS technology with such significance to human health,” said Jim Kapron, Strategic Marketing Specialist at Thermo Fisher Scientific.

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LC-MSLC-MS (liquid chromatography-mass spectrometry) systems and equipment are used for separation and quantitative analysis of complex mixtures, combining liquid chromatography and mass spectrometry. Quantify proteins, contaminants, pesticides or screen for drug metabolites with a high level of sensitivity. LC-MS systems and equipment include reverse phase, normal phase and specialized columns integrated with various MS detectors such as time-of-flight (TOF), quadrupole, orbitrap or ion trap mass analyzers. LC-MS/MS instruments equipped with a qTOF or triple quadrupole analyzer give greater sensitivity and resolving power to your analysis. Find the best LC-MS equipment in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Mass SpectrometryMass spectrometry (MS) is a powerful analytical technique used to identify and quantify molecules based on the mass-to-charge ratio of gas-phase ions. It provides detailed information about the structure, composition, and properties of compounds and is widely used across fields such as environmental monitoring, materials science, drug discovery and development, food and beverage testing, and wider chemical research. Key MS techniques include tandem mass spectrometry (MS/MS), liquid chromatography–mass spectrometry (LS-MS) and inductively coupled plasma (ICP-MS). Choosing from these wide range of techniques and technologies can be a daunting task, so keep up to date with scientific applications, performance expectations, and customer reviews here all in one place. Visit our product directory to receive quotes direct from the manufacturer. Medicinal ChemistryMedicinal chemistry is a broad discipline encompassing the design, identification, synthesis and development of chemicals in drug discovery. It includes a number of techniques covering structural biology, synthetic chemistry and molecular biology. Technologies used in medicinal chemistry include ADME, lab-on-a-chip, high content screening and assay assembly.
Thermo Fisher Scientific’s FAIMS-based LC/MS Analytical Method is Validated by A&M Labor fuer Analytik to Ensure Human Safety in Drug Development