Chromatography 6329 223695138 2008-07-05T08:50:22Z Slashme 451287 /* Thin layer chromatography */ Note HPTLC {{for|the Second Person album|Chromatography (album)}} [[Image:chromatography00.jpg|thumb|Pictured is a sophisticated gas chromatography system. This instrument records concentrations of acrylonitrile in the air at various points throughout the chemical laboratory.]] '''Chromatography ''' (from [[Greek language|Greek]] χρώμα:''chroma'', color and γραφειν:"graphein" to write) is the collective term for a family of [[laboratory techniques]] for the [[separation of mixtures]]. It involves passing a mixture dissolved in a "mobile phase" through a ''stationary phase'', which separates the [[analyte]] to be measured from other molecules in the mixture and allows it to be isolated. Chromatography may be preparative or analytical. Preparative chromatography seeks to separate the components of a mixture for further use (and is thus a form of purification). Analytical chromatography normally operates with smaller amounts of material and seeks to measure the relative proportions of analytes in a mixture. The two are not mutually exclusive. == Explanation == {{wiktionary|chromatography}} An analogy which is sometimes useful is to suppose a mixture of bees and wasps passing over a flower bed. The bees would be more attracted to the flowers than the wasps, and would become separated from them. If one were to observe at a point past the flower bed, the wasps would pass first, followed by the bees. In this analogy, the bees and wasps represent the analytes to be separated, the flowers represent the stationary phase, and the mobile phase could be thought of as the air. The key to the separation is the differing affinities among analyte, stationary phase, and mobile phase. The observer could represent the detector used in some forms of analytical chromatography. A key point is that the detector need not be capable of discriminating between the analytes, since they have become separated before passing the detector. == History == It was the [[Russia]]n [[botanist]] [[Mikhail Tsvet|Mikhail Semyonovich Tsvet]] who invented the first chromatography technique in 1900 during his research on [[chlorophyll]]. He used a liquid-adsorption column containing [[calcium carbonate]] to separate plant [[pigment]]s. The method was described on [[December 30]] [[1901]] at the 11th Congress of Naturalists and Doctors (XI съезд естествоиспытателей и врачей) in [[Saint Petersburg]]. The first printed description was in 1903, in the Proceedings of the [[Warsaw]] Society of Naturalists, section of biology. He first used the term ''chromatography'' in print in 1906 in his two papers about chlorophyll in the German botanical journal, ''Berichte der Deutschen Botanischen Gesellschaft''. In 1907 he demonstrated his chromatograph for the German Botanical Society. Interestingly, Mikhail's surname "Цвет" means "color" in Russian, so there is the possibility that his naming the procedure chromatography (literally "color writing") was a way that he could make sure that he, a commoner in Tsarist Russia, could be immortalized. In 1952 [[Archer John Porter Martin]] and [[Richard Laurence Millington Synge]] were awarded the Chemistry Nobel Prize for their invention of partition chromatography.<ref>[http://www.nobel.se/chemistry/laureates/1952/ Nobelprize.org: The Nobel Prize in Chemistry 1952]</ref> Since then, the technology has advanced rapidly. Researchers found that the principles underlying Tsvet's chromatography could be applied in many different ways, giving rise to the different varieties of chromatography described below. Simultaneously, advances continually improved the technical performance of chromatography, allowing the separation of increasingly similar molecules. In 1987 Pedro Cuatrecasas and [[Meir Wilchek]] were awarded the [[Wolf Prize in Medicine]] for the invention and development of [[affinity chromatography]] and its applications to biomedical sciences. ==Chromatography terms== * The '''analyte''' is the substance that is to be separated during chromatography. * '''Analytical chromatography''' is used to determine the existence and possibly also the concentration of analyte(s) in a sample. * A '''bonded phase''' is a stationary phase that is covalently bonded to the support particles or to the inside wall of the column tubing. * A '''chromatogram''' is the visual output of the chromatograph. In the case of an optimal separation, different peaks or patterns on the chromatogram correspond to different components of the separated mixture. :[[Image:Rt 5 9.png|300px|Chromatogram with unresolved peaks]][[Image:Rt 5 12.png|300px|Chromatogram with two resolved peaks]] :Plotted on the x-axis is the retention time and plotted on the y-axis a signal (for example obtained by a [[Spectrophotometry|spectrophotometer]], [[Mass Spectrometry|mass spectrometer]] or a variety of other detectors) corresponding to the response created by the analytes exiting the system. In the case of an optimal system the signal is proportional to the concentration of the specific analyte separated. * A '''chromatograph''' is equipment that enables a sophisticated separation e.g. gas chromatographic or liquid chromatographic separation. * '''Chromatography''' is a physical method of separation in which the components to be separated are distributed between two phases, one of which is stationary (stationary phase) while the other (the mobile phase) moves in a definite direction. * The '''effluent''' is the mobile phase leaving the column. * An '''immobilized phase''' is a stationary phase which is immobilized on the support particles, or on the inner wall of the column tubing. * The '''mobile phase''' is the phase which moves in a definite direction. It may be a liquid (LC and CEC), a gas (GC), or a supercritical fluid (supercritical-fluid chromatography, SFC). A better definition: The mobile phase consists of the sample being separated/analyzed and the solvent that moves the sample through the column. In one case of HPLC the solvent consists of a carbonate/bicarbonate solution and the sample is the anions being separated. The mobile phase moves through the chromatography column (the stationary phase) where the sample interacts with the stationary phase and is separated. * '''Preparative chromatography''' is used to purify sufficient quantities of a substance for further use, rather than analysis. * The '''retention time''' is the characteristic time it takes for a particular analyte to pass through the system (from the column inlet to the detector) under set conditions. See also: [[Kovat's retention index]] * The '''sample''' is the matter analysed in chromatography. It may consist of a single component or it may be a mixture of components. When the sample is treated in the course of an analysis, the phase or the phases containing the analytes of interest is/are referred to as the sample whereas everything out of interest separated from the sample before or in the course of the analysis is referred to as waste. * The '''solute''' refers to the sample components in partition chromatography. * The '''solvent''' refers to any substance capable of solubilizing other substance, and especially the liquid mobile phase in LC. * The '''stationary phase''' is the substance which is fixed in place for the chromatography procedure. Examples include the [[silica]] layer in [[Chromatography#Thin layer chromatography|thin layer chromatography]]. ==Techniques by chromatographic bed shape== ===Column chromatography=== {{details|Column chromatography}} [[Image:columnchromatography.gif|thumb|right|300px|A diagram of a standard column chromatography and a flash column chromatography setup]] Column chromatography is a separation technique in which the stationary bed is within a tube. The particles of the solid stationary phase or the support coated with a liquid stationary phase may fill the whole inside volume of the tube (packed column) or be concentrated on or along the inside tube wall leaving an open, unrestricted path for the mobile phase in the middle part of the tube (open tubular column). Differences in rates of movement through the medium are calculated to different retention times of the sample.<ref>[http://www.iupac.org/publications/pac/1993/pdf/6504x0819.pdf IUPAC Nomenclature for Chromatography] IUPAC Recommendations 1993, Pure & Appl. Chem., Vol. 65, No. 4, pp.819-872, 1993. </ref> In 1978, W. C. Still introduced a modified version of column chromatography called '''flash column chromatography''' (flash).<ref>Still, W. C.; Kahn, M.; Mitra, A. ''[[J. Org. Chem.]]'' '''1978''', ''43(14)'', 2923-2925. ({{DOI|10.1021/jo00408a041}})</ref> The technique is very similar to the traditional column chromatography, except for that the solvent is driven through the column by applying positive pressure. This allowed most separations to be performed in less than 20 minutes, with improved separations compared to the old method. Modern flash chromatography systems are sold as pre-packed plastic cartridges, and the solvent is pumped through the cartridge. Systems may also be linked with detectors and fraction collectors providing automation. The introduction of gradient pumps resulted in quicker separations and less solvent usage. In [[expanded bed adsorption]], a fluidized bed is used, rather than a solid phase made by a packed bed. This allows omission of initial clearing steps such as centrifugation and filtration, for culture broths or slurries of broken cells. ===Planar Chromatography=== [[Image:Chromatography of chlorophyll - Step 7.jpg|right|thumb|75px|Thin layer chromatography is used to separate components of [[chlorophyll]]]] '''Planar chromatography''' is a separation technique in which the stationary phase is present as or on a plane. The plane can be a paper, serving as such or impregnated by a substance as the stationary bed ([[paper chromatography]]) or a layer of solid particles spread on a support such as a glass plate ([[thin layer chromatography]]). ====Paper Chromatography==== {{details|Paper chromatography}} Paper chromatography is a technique that involves placing a small dot of sample solution onto a strip of ''[[chromatography paper]]''. The paper is placed in a jar containing a shallow layer of [[solvent]] and sealed. As the solvent rises through the paper it meets the sample mixture which starts to travel up the paper with the solvent. Different [[chemical compound|compounds]] in the sample mixture travel different distances according to how strongly they interact with the paper. This paper is made of cellulose, a polar molecule, and the compounds within the mixture travel farther if they are non-polar. More polar substances bond with the cellulose paper more quickly, and therefore do not travel as far. This process allows the calculation of an R<sub>f</sub> value and can be compared to standard compounds to aid in the identification of an unknown substance. ====Thin layer chromatography====<!-- This section is linked from [[Chromatography]] --> {{details|Thin layer chromatography}} Thin layer chromatography (TLC) is a widely-employed laboratory technique and is similar to [[paper chromatography]]. However, instead of using a stationary phase of paper, it involves a stationary phase of a thin layer of adsorbent like [[silica gel]], [[aluminium oxide|alumina]], or [[cellulose]] on a flat, inert substrate. Compared to paper, it has the advantage of faster runs, better separations, and the choice between different adsorbents. Different [[chemical compound|compounds]] in the sample mixture travel different distances according to how strongly they interact with the adsorbent. This allows the calculation of an R<sub>f</sub> value and can be compared to standard compounds to aid in the identification of an unknown substance. For even better resolution and to allow for quantitation, [[HPTLC|high-performance TLC]] can be used. ==Techniques by physical state of mobile phase== === Gas chromatography ===<!-- This section is linked from [[Biodiesel]] --> {{details|Gas chromatography}} Gas chromatography (GC), also sometimes known as Gas-Liquid chromatography, (GLC), is a separation technique in which the mobile phase is a gas. Gas chromatography is always carried out in a column, which is typically "packed" or "capillary" (see below) . Gas chromatography (GC) is based on a [[partition equilibrium]] of analyte between a solid stationary phase (often a liquid silicone-based material) and a mobile gas (most often Helium). The stationary phase is adhered to the inside of a small-diameter glass tube (a capillary column) or a solid matrix inside a larger metal tube (a packed column). It is widely used in [[analytical chemistry]]; though the high temperatures used in GC make it unsuitable for high molecular weight biopolymers or proteins (heat will denature them), frequently encountered in [[biochemistry]], it is well suited for use in the [[petrochemical]], environmental monitoring, and [[Chemical industry|industrial chemical]] fields. It is also used extensively in chemistry research. === Liquid chromatography === Liquid chromatography (LC) is a separation technique in which the mobile phase is a liquid. Liquid chromatography can be carried out either in a column or a plane. Present day liquid chromatography that generally utilizes very small packing particles and a relatively high pressure is referred to as [[high performance liquid chromatography]] (HPLC). In the HPLC technique, the sample is forced through a column that is packed with irregularly or spherically shaped particles or a porous monolithic layer (stationary phase) by a liquid (mobile phase) at high pressure. HPLC is historically divided into two different sub-classes based on the polarity of the mobile and stationary phases. Technique in which the stationary phase is more polar than the mobile phase (e.g. toluene as the mobile phase, silica as the stationary phase) is called normal phase liquid chromatography (NPLC) and the opposite (e.g. water-methanol mixture as the mobile phase and C18 = octadecylsilyl as the stationary phase) is called reversed phase liquid chromatography (RPLC). Ironically the "normal phase" has fewer applications and RPLC is therefore used considerably more. Specific techniques which come under this broad heading are listed below. It should also be noted that the following techniques can also be considered [[fast protein liquid chromatography]] if no pressure is used to drive the mobile phase through the stationary phase. See also [[Aqueous Normal Phase Chromatography]]. ==Affinity chromatography== {{details|Affinity chromatography}} Affinity chromatography<ref>Pascal Bailon, George K. Ehrlich, Wen-Jian Fung and Wolfgang Berthold, An Overview of Affinity Chromatography, Humana Press, 2000. ISBN 978-0-89603-694-9, ISBN 978-1-60327-261-2. </ref> is based on selective non-covalent interaction between an analyte and specific molecules. It is very specific, but not very [[robust]]. It is often used in biochemistry in the purification of [[protein]]s bound to tags. These [[fusion protein]]s are labelled with compounds such as [[His-tag]]s, [[biotin]] or [[antigen]]s, which bind to the stationary phase specifically. After purification, some of these tags are usually removed and the pure protein is obtained. === Supercritical fluid chromatography === {{details|Supercritical fluid chromatography}} Supercritical fluid chromatography is a separation technique in which the mobile phase is a fluid above and relatively close to its critical temperature and pressure. == Techniques by separation mechanism== === Ion exchange chromatography === {{details|Ion exchange chromatography}} Ion exchange chromatography utilizes ion exchange mechanism to separate analytes. It is usually performed in columns but the mechanism can be benefited also in planar mode. Ion exchange chromatography uses a charged stationary phase to separate charged compounds including [[amino acid]]s, [[peptide]]s, and [[protein]]s. In conventional methods the stationary phase is an [[ion exchange resin]] that carries charged [[functional group]]s which interact with oppositely charged groups of the compound to be retained. Ion exchange chromatography is commonly used to purify proteins using [[fast protein liquid chromatography|FPLC]]. === Size exclusion chromatography === {{details|Size exclusion chromatography}} Size exclusion chromatography (SEC) is also known as '''gel permeation chromatography''' (GPC) or '''gel filtration chromatography''' and separates molecules according to their size (or more accurately according to their hydrodynamic diameter or hydrodynamic volume). Smaller molecules are able to enter the pores of the media and, therefore, take longer to elute, whereas larger molecules are excluded from the pores and elute faster. It is generally a low resolution chromatography technique and thus it is often reserved for the final, "polishing" step of a purification. It is also useful for determining the [[tertiary structure]] and [[quaternary structure]] of purified proteins, especially since it can be carried out under native [[solution]] conditions. ==Special techniques == ===Reversed-phase chromatography=== {{details|Reversed-phase chromatography}} Reversed-phase chromatography is an elution procedure used in liquid chromatography in which the mobile phase is significantly more polar than the stationary phase. ===Two-dimensional chromatography=== In some cases, the chemistry within a given column can be insufficient to separate some analytes. It is possible to direct a series of unresolved peaks onto a second column with different physico-chemical ([[Chemical classification]]) properties. Since the mechanism of retention on this new solid support is different from the first dimensional separation, it can be possible to separate compounds that are indistinguishable by one-dimensional chromatography. ===Simulated Moving-Bed Chromatography=== {{details|Simulated moving bed}} ===Pyrolysis gas chromatography=== ===Fast protein liquid chromatography=== {{details|Fast protein liquid chromatography}} Fast protein liquid chromatography (FPLC) is a term applied to several chromatography techniques which are used to purify proteins. Many of these techniques are identical to those carried out under high performance liquid chromatography, however use of FPLC techniques are typically for preparing large scale batches of a purified product. === Countercurrent chromatography === {{details|Countercurrent chromatography}} Countercurrent chromatography (CCC) is a type of liquid-liquid chromatography, where both the stationary and mobile phases are liquids. It involves mixing a solution of liquids, allowing them to settle into layers and then separating the layers. === Chiral chromatography === Chiral chromatography involves the separation of stereoisomers. In the case of enantiomers, these have no chemical or physical differences apart from being three dimensional mirror images. Conventional chromatography or other separation processes are incapable of separating them. To enable chiral separations to take place, either the mobile phase or the stationary phase must themselves be made chiral, giving differing affinities between the analytes. Chiral chromatography HPLC columns (with a chiral stationary phase) in both normal and reversed phase are commercially available. ==See also== {{Separation processes}} * [[wikibooks:Transwiki:Paper chromatography of amino acids|Paper chromatography of amino acids]] on [[Wikibooks]] * [[Aqueous Normal Phase Chromatography]] * [[Multicolumn countercurrent solvent gradient purification]] (MCSGP) * [[Chromatography in blood processing]] * [[Chromatography software]] ==References== {{reflist}} ==External links== {{Commonscat|Chromatography}} * [http://www.iupac.org/publications/pac/1993/pdf/6504x0819.pdf IUPAC Nomenclature for Chromatography] * [http://www.chromedia.org Chromedia]On line database and community for chromatography practitioners * [http://wetenschap.infonu.nl/scheikunde/18559-hydrofobe-interactie-chromatografie.html Reversed phase chromatography article (dutch)] * [http://www.chromatography-online.org/ Library 4 Science: Chrom-Ed Series] * [http://www.vias.org/simulations/simusoft_peakoverlap.html Overlapping Peaks Program - Learning by Simulations] * [http://ocw.mit.edu/ans7870/resources/chemvideo/index.htm Chromatography Videos - MIT OCW - Digital Lab Techniques Manual] * [http://kubrick.colorado.edu:6060/ramgen/chemistry/GasChromatography.rm GC Video - University of Colorado] * [http://www.mtc-usa.com/calculators_chrom.asp Chromatography Equations Calculators - MicroSolv Technology Corporation] {{Analytical chemistry}} {{pathology}} [[Category:Chemical pathology]] [[Category:Chromatography]] [[Category:Separation processes]] [[Category:Biological techniques and tools]] [[Category:Russian inventions]] {{Link FA|bs}} [[ar:كروماتوجرافيا]] [[bs:Hromatografija]] [[ca:Cromatografia]] [[cs:Chromatografie]] [[de:Chromatografie]] [[es:Cromatografía]] [[eu:Kromatografia]] [[fa:کروماتوگرافی]] [[fr:Chromatographie]] [[gl:Cromatografía]] [[id:Kromatografi]] [[it:Cromatografia]] [[he:כרומטוגרפיה]] [[hu:Kromatográfia]] [[ms:Kromatografi]] [[nl:Chromatografie]] [[ja:クロマトグラフィー]] [[no:Kromatografi]] [[nn:Kromatografi]] [[oc:Cromatografia]] [[pl:Chromatografia]] [[pt:Cromatografia]] [[ru:Хроматография]] [[simple:Chromatography]] [[sk:Chromatografia]] [[sl:Kromatografija]] [[sr:Хроматографија]] [[fi:Kromatografia]] [[sv:Kromatografi]] [[vi:Sắc kí]] [[tr:Kromatografi]] [[uk:Хроматографія]] [[zh:色谱法]]