Procedure by which solutes (e.g., proteins and other chemical products) are selectively separated by a dynamic differential migration process in a system consisting of two or more phases, one of which moves continuously in a given direction and in which the individual substances exhibit different mobilities by reason of differences in adsorption, partition, solubility, vapor pressure, molecular size, or ionic charge density. The individual substances thus obtained can be identified or determined by analytical methods. There are several types of chromatography in use with different operating principles:1.Adsorption – separates products by their different affinities for the surface of a solid medium, either an inorganic carrier such as silica gel, alumina, or hydroxyapatite, or an organic polymer.2.Ion Exchange – uses ion exchange resin to which ionized functional groups have been attached. At an appropriate pH, target proteins acquire a net surface charge that allows them to selectively bind to an ion exchange resin. Other impurities are eluted through the column.3.Gel Filtration – employs a neutral cross-linked carrier with a defined pore size for molecular fractionation. Molecules larger than the largest pores cannot enter the matrix and pass directly through the column; smaller molecules enter the carrier and are retarded. Gel filtration thus separates on the basis of molecular size, eluting larger molecules first, followed by progressively smaller species. (also see: Exclusion Limit)4.Affinity – relies on the propensity of each biomolecule to have an affinity for another highly specific biomolecule, such as an antibody-antigen relationship. Once bound together, the drug molecules can be detached by altering various chemical attributes in the column.5.Hydrophobic – separates by molecule polarity and reverse interaction with water.6.High Pressure Liquid Chromatography (HPLC).