Chromatography is an analytical chemical technique used for the separation, identification, and purification of compounds in a complex mixture. It is an important biophysical technique used for qualitative and quantitative analysis.
All types of chromatography techniques has two phases- a stationary and a mobile phase. The stationary phase contains the mixture while the mobile phase carries the components in the mixture as it passes through. The compounds in the mixture separate at different paces as they pass through the mobile phase.
Chromatography can be used for the separation of any chemical in liquid, solid, or gaseous phases, using specific stationary and mobile phases. The characteristic time for the passage of each component is called retention time.
Depending on the retention time each component travels at different levels which leads to the separation of the compounds.
Chromatographic techniques are categorized based on several criteria. There are different types based on the chosen stationary and mobile phases and the chosen method. Based on the stationary and mobile phases chosen, there are different types of chromatography techniques.
Based on the method used, chromatography can be categorized into,
Gas chromatography is used for separating volatile compounds. A non-volatile stationary phase such as silicone oils, grease, paraffin, apiezon oils, etc., is used here. An inert gas is used as the mobile phase which will pass through the other one and carries the separated compounds with it.
The column used here could be a capillary or a packed column. For the latter, the columns are packed with fine, solid, inert particles such as diatomaceous earth. This diatomaceous earth is coated with the liquid stationary phase.
The capillary column can be a Wall Coated Open Tubular (WCOT) or Support Coated Open Tubular (SCOT). The former has its wall coated with the liquid stationary phase while the latter has its wall lined with a thin layer of diatomaceous earth where the stationary phase is adsorbed. The capillary columns are more efficient than the packed columns.
Column chromatography uses a column to separate the compounds.
Flash gas chromatography is simple and works faster. It uses a narrow glass tube where the flow of the solvent can be controlled by a pressure valve at the top or a suction at the bottom.
The stationary phase of flash golem chromatography requires smaller particles than what is used in column chromatography. It uses silica, reverse silica, cellulose, etc as the stationary phase depending on the nature of the compounds.
The working mechanism is the same as that in the column chromatography.
TLC is the common type of chromatographic technique used for the quantitative analysis of compounds. It is simpler and faster than other types of chromatography. The stationary phase uses a thin layer of silica, cellulose, or alumina, coated on a glass plate, aluminum foil, plastic sheet, etc.
HPTLC stands for High-Performance Thin Layer Chromatography, which is an upgraded version of normal TLC. This is an automated setup used for quantitative and qualitative analysis of compounds. Precoated plates with silica gel coating are used here as the stationary phase. The reverse phase mode uses C18, C8, etc.
HPTLC is more efficient than TLC since the adsorbents have uniform size and are smaller. It needs just a tiny spot of sample but it has to be more concentrated.
A semiautomatic loading apparatus such as the Linomat V apparatus is usually used to load the sample. HPTLC can be done in linear development chambers where the chromatogram can be developed from the sides.
It is usually used for the standardization of herbal formulations and extracts. Moreover, it helps develop the analytical profile of anthracene, lipids, alkaloids, flavonoids, steroids, etc.
HPLC is similar to Flash column chromatography but uses high pressure to move the mobile phase. Instead of a glass column, HPLC uses a steel column that can withstand high pressure.
It is suitable for all types of liquid chromatography. The HPLC will be connected to a spectrometer that helps study the spectral characters of the compounds that are separated.
HPLC is advantageous over gas chromatography as the sample can be recovered after the analysis and purification.
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