Gas Chromatography (GC)

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There 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.

As 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.

Bob McDowall stresses the importance of using accurate and precise time and date stamps to ensure the integrity of the data and results generated by computerized systems in any chromatography laboratory.

In this article, Jo Webber tackles the problem of ensuring data integrity in pharmaceutical manufacturing. She shows how, by using modern technology and well integrated systems, quality can be improved.

Protease inhibitors are a class of anti-HIV drugs used in combination therapy to block replication of the HIV virus in a person's blood. It is important to monitor the levels of these drugs in the patient since resistance can develop at low levels and at high levels the drug can exhibit toxic effects.

In the concluding part of this series, the effects that column variability has on isothermal capillary gas chromatography is discussed and instrument calibration explored. The goal is to reduce the normal variability that occurs when working with multiple instruments and columns to ensure consistent results.

Pittcon 2005 - the 56th Pittsburgh Conference on Analytical Chemistry and Applied Spectroscopy - returned to the Orange County Convention Center, Orlando, Florida, 27 February-4 March 2005. This year's event hosted more than 900 instrument manufacturers and 1aboratory suppliers in more than 2300 booths. In addition to attending the exposition, the conferees were able to listen to numerous oral presentations, view more than 900 posters, check out 38 seminar rooms, or attend one of 150 short courses.

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This month's installment of "Milestones in Chromatography" pays tribute to a true milestone in the evolution of chromatography: the introduction of the first successful GC instruments.

This instalment of GC Connections examines the basics of peak identification and quantification and demonstrates how they can both influence the quality of one's results as much as or even more than sample preparation, separation and detection.

In response to a reader's question, John Hinshaw examines the effects on retention times and peak shapes when a retention gap is added to a capillary column.