November 27th 2024
During RAFA 2024, we interviewed Giorgia Purcaro of the University of Liège about using multidimensional gas chromatography (GC) to analyze mineral oil hydrocarbons (MOH).
Market Profile: Pharmaceutical Market Demand for Life Science Instrumentation
May 1st 2006Globally, 2005 sales of pharmaceuticals have been estimated at approximately $550 billion. A significant fraction of this amount was due to the top pharmaceutical companies in the world. The top five companies alone were responsible for total revenues of $168 billion, or 30% of the entire market.
The Rise and Fall of Expertise in Gas Chromatography
May 1st 2006Guest columnist Walter Jennings reflects on the early days of capillary gas chromatography (GC) and how chromatographers become experts in the technology by constructing their own columns, thereby achieving a more thorough understanding of the chromatographic process.
Chromatography for Bioanalytical Chemists
May 1st 2006This article looks at current practices in bioanalytical chemistry by examining and critically assessing the various parameters that can be altered to achieve high-speed results with high resolution in LC–MS applications. The decision to opt for gradient or isocratic elution is also discussed.
Novel Applications and New Developments in Gas Chromatography
March 14th 2006Exciting new uses for gas chromatography and its hyphenated forms show that there is an uncharted territory of applications and that there are limitations that still need to be overcome. The Tuesday afternoon oral session at Pittcon 2006, "GC-MS: Developments and Applications," gave the audience an idea of advances in GC and some new areas for the technique's application. John Chalmers of VS Consulting (Stokesley, United Kingdom) presided over the session.
Successful Gas Chromatography Using Fused-Silica Capillary Columns
March 1st 2006Capillary gas chromatography (GC) is a well-established separation technique. Rick Parmely reviews some of the capillary column basics by investigating a standard test mixture and observing some of the chromatographic effects that can affect peak response, peak shape and column bleed. He provides guidelines for obtaining the best performance from a capillary column. He discusses peak tailing, column overload, ghost peaks and column bleed and speculates on "when to give up." He concludes with a set of fundamental steps to be used in achieving better GC analyses.
Analysis of Volatile Bacterial Metabolites by Gas Chromatography–Mass Spectrometry
A method for the identification of key volatile organic compound (VOC) markers associated with infection by Neisseria meningitidis bacteria by gas chromatography–mass spectrometry (GC–MS) was developed. Headspace samples of bacterial VOCs were trapped on triple-sorbent bed tubes and then thermally desorbed into a laboratory GC–MS system for separation. Identification was carried out by comparison of GC retention time and electron ionization mass spectra to the National Institute of Standards and Technology (NIST) database. Further confirmation was obtained by GC–MS of known standard chemicals. A total of 75 VOCs were detected, five of which can be considered key VOC markers for Neisseria meningitidis. These peaks were identified as 1,2-dimethylcyclopropane, 2-methylpropanal, methacrolein, N-2-dimethyl-1-propanamine, and 3-methylbutanal by the NIST database.
Successful Gas Chromatography Using Fused-Silica Capillary Columns
November 1st 2005guest Columnist Rick Parmely takes a look at some capillary column basics of a well-established separation technique. He discusses peak tailing, column overload, ghost peaks, and column bleed, and speculates on "when to give up."
How To Buy Gas Calibration Mixes
October 1st 2005In January 2004, LCGC Europe published an article on methods for selecting pure gases for analytical applications. 1 Here, the authors expand on this topic by addressing questions regarding gas mixtures - defined simply as more than one gas in a cylinder.
Benchmarking for Analytical Methods: The Horwitz Curve
October 1st 2005Analytical chemists are concerned with the quality of their methods and results. An important question in this context is whether the precision of a newly developed and validated method is up to standard. In other words: is the precision of the newly developed method comparable to what could be expected? This article looks at how the Horwitz equation can answer this. It also describes the results of an extensive study involving 10000 laboratories which indicates that the relative reproducibility approximately doubles for every 100-fold decrease in concentration and that, surprisingly, it does not depend on the type of material or method.
Cost Beneficial Validation of a Site-wide Chromatography Data System
September 1st 2005The implementation and validation of a new site-wide chromatography data system for a major active pharmaceutical ingredient custom manufacturer provided the opportunity to map and optimize the GMP and ISO business processes to use electronic signatures effectively. This article describes the process optimization and how it integrates with the validation activities of the system. This overall approach provides substantial business benefits from the use of electronic signatures as evidenced by the savings resulting from process improvement and by the fact that the non-GMP laboratories implemented a similar process to analyse and approve results electronically.
How To Buy Gas Calibration Mixes
July 1st 2005There is a great deal of confusion floating about when it comes to selecting gas mixtures for analytical applications. Questions such as "How is the gas certified?," "What standard should I use?," and "What level of uncertainty is acceptable?" are common concerns heard among those tasked with specifying and using mixtures. In addition, the uncertainty regarding terminology, measurement, safety, and storage can make specifying mixtures a true source of headaches and hassles for any lab manager. The following article provides answers to questions about gas mixtures.
Enhanced Sample Throughput for Environmental Analysis
June 1st 2005As environmental legislation becomes more stringent, the need to deliver quantitative results in shorter times and greater volumes is necessary for routine environmental analysis. Most of the high-throughput screening methods used to analyze pharmaceutical compounds are, however, useless for environmental monitoring. This is because these methods primarily aim to retrieve as much information from a single sample using the broadest range of techniques. The chromatographic separation process is considered to be the bottleneck in the process. This is not the situation for environmental procedures, in which the bottleneck is the sample preparation step and is usually very tedious and time-consuming.
Determining the Hydrocarbon Oil Index in Water using Ultra Fast Gas Chromatography
June 1st 2005This article discusses utra fast gas chromatography as a suitable technique for determining the hydrocarbon oil index in water. The advantages of this technique over conventional GC technology are presented.