GC/MS combines gas chromatography and mass spectrometry to identify and quantify drugs. Gas chromatography separates drugs in a sample using a helium gas stream moving through a column. Each drug has a unique retention time. Mass spectrometry then fragments the drugs and analyzes the fragmentation patterns, which are also unique molecular fingerprints. An internal standard with similar chemical properties is added for quantification and qualification, and the ideal standard is a deuterated version of the drug to differentiate it during analysis. By using retention time, fragmentation pattern, and internal standard information, GC/MS provides multidimensional identification and is the leading confirmation method for forensic drug testing.
GC/MS combines gas chromatography and mass spectrometry to identify and quantify drugs. Gas chromatography separates drugs in a sample using a helium gas stream moving through a column. Each drug has a unique retention time. Mass spectrometry then fragments the drugs and analyzes the fragmentation patterns, which are also unique molecular fingerprints. An internal standard with similar chemical properties is added for quantification and qualification, and the ideal standard is a deuterated version of the drug to differentiate it during analysis. By using retention time, fragmentation pattern, and internal standard information, GC/MS provides multidimensional identification and is the leading confirmation method for forensic drug testing.
GC/MS combines gas chromatography and mass spectrometry to identify and quantify drugs. Gas chromatography separates drugs in a sample using a helium gas stream moving through a column. Each drug has a unique retention time. Mass spectrometry then fragments the drugs and analyzes the fragmentation patterns, which are also unique molecular fingerprints. An internal standard with similar chemical properties is added for quantification and qualification, and the ideal standard is a deuterated version of the drug to differentiate it during analysis. By using retention time, fragmentation pattern, and internal standard information, GC/MS provides multidimensional identification and is the leading confirmation method for forensic drug testing.
GC/MS combines gas chromatography and mass spectrometry to identify and quantify drugs. Gas chromatography separates drugs in a sample using a helium gas stream moving through a column. Each drug has a unique retention time. Mass spectrometry then fragments the drugs and analyzes the fragmentation patterns, which are also unique molecular fingerprints. An internal standard with similar chemical properties is added for quantification and qualification, and the ideal standard is a deuterated version of the drug to differentiate it during analysis. By using retention time, fragmentation pattern, and internal standard information, GC/MS provides multidimensional identification and is the leading confirmation method for forensic drug testing.
GC/MS is a combination of two different analytical techniques, Gas Chromatography and
Mass Spectrometry. GC/MS, with the use of internal standards, provides a multidimensional drug identification and quantitation procedure that is the leading confirmation method for forensic drug testing. Gas Chromatography (GC): Gas Chromatography is a technique used to separate drugs that might be present in a sample. The sample is injected into a long tubular column, the chromatography column. The drugs are swept through the column by a stream of helium gas. Drugs in a sample are separated from each other because some take longer to pass through the column than others. The process is like a race around a track: at the beginning the racers are all together in a group and at the end they are all separated with the fast ones finishing far in advance of the slow ones. A drugs individual chemical characteristic determines how long it will take to go through the chromatography column. The time it takes for any given drug to travel the length of the column is referred to as its retention time (RT). The RT for a given drug is an identifying characteristic. Mass Spectrometry (MS): The detector for the GC is the Mass Spectrometry (MS) detector. As a drug exits the end of the GC column it is fragmented by ionization and the fragments are sorted by mass to form a fragmentation pattern. Like the retention time (RT), the fragmentation pattern for a given drug is unique and therefore is an identifying characteristic of the drug. It is so specific that it is often referred to as the molecular fingerprint. Internal Standard (I.S.): An Internal Standard (I.S.) is a drug with similar chemical characteristics to the one being assayed. A precise amount of an I.S. is added to a sample before it is prepared so that the I.S. is prepared and analyzed in the identical way as the drug. During analysis, the signal produced by the I.S. is compared to the signal produced by the drug in question in order to quantify the drug and to qualify the assay. The ideal internal standard is a deuterated version of the drug in question. Deuterium is an isotope of hydrogen that has a mass of 1 atomic unit more than hydrogen. A deuterated drug is manufactured with one or more hydrogen atoms substituted with a deuterium atom. The deuterated I.S. exhibits the same chemical characteristics during the sample preparation, and the same RT during GC analysis as a non-deuterated drug, but can be differentiated by the MS detector due to the mass of the fragments. Only a GC/MS can utilize a deuterated I.S. The identification of a drug by its retention time (gas chromatography) and fragmentation pattern (mass spectrometry), along with sample specific information afforded by the presence of the deuterated IS combine to make GC/MS the foremost confirmation method for forensic drug testing. 1