High-performance liquid chromatography

A modern self-contained HPLC
Schematic representation of an HPLC unit (1) solvent reservoirs, (2) solvent degasser, (3) gradient valve, (4) mixing vessel for delivery of the mobile phase, (5) high-pressure pump, (6) switching valve in "inject position", (6') switching valve in "load position", (7) sample injection loop, (8) pre-column (guard column), (9) analytical column, (10) detector (i.e., IR, UV), (11) data acquisition, (12) waste or fraction collector.

High-performance liquid chromatography (HPLC), formerly referred to as high-pressure liquid chromatography, is a technique in analytical chemistry used to separate, identify, and quantify specific components in mixtures. The mixtures can originate from food, chemicals, pharmaceuticals,[1] biological, environmental and agriculture, etc., which have been dissolved into liquid solutions.

It relies on high pressure pumps, which deliver mixtures of various solvents, called the mobile phase, which flows through the system, collecting the sample mixture on the way, delivering it into a cylinder, called the column, filled with solid particles, made of adsorbent material, called the stationary phase.

Each component in the sample interacts differently with the adsorbent material, causing different migration rates for each component. These different rates lead to separation as the species flow out of the column into a specific detector such as UV detectors. The output of the detector is a graph, called a chromatogram. Chromatograms are graphical representations of the signal intensity versus time or volume, showing peaks, which represent components of the sample. Each sample appears in its respective time, called its retention time, having area proportional to its amount.

HPLC is widely used for manufacturing (e.g., during the production process of pharmaceutical and biological products),[2][3] legal (e.g., detecting performance enhancement drugs in urine),[4] research (e.g., separating the components of a complex biological sample, or of similar synthetic chemicals from each other), and medical (e.g., detecting vitamin D levels in blood serum) purposes.[5]

Chromatography can be described as a mass transfer process involving adsorption and/or partition. As mentioned, HPLC relies on pumps to pass a pressurized liquid and a sample mixture through a column filled with adsorbent, leading to the separation of the sample components. The active component of the column, the adsorbent, is typically a granular material made of solid particles (e.g., silica, polymers, etc.), 1.5–50 μm in size, on which various reagents can be bonded. The components of the sample mixture are separated from each other due to their different degrees of interaction with the adsorbent particles. The pressurized liquid is typically a mixture of solvents (e.g., water, buffers, acetonitrile and/or methanol) and is referred to as a "mobile phase". Its composition and temperature play a major role in the separation process by influencing the interactions taking place between sample components and adsorbent. These interactions are physical in nature, such as hydrophobic (dispersive), dipole–dipole and ionic, most often a combination.

  1. ^ Kazakevich, Yuri; LoBrutto, Rosario, eds. (2007). HPLC for pharmaceutical scientists. Hoboken, NJ: Wiley-Interscience. ISBN 978-0-471-68162-5.
  2. ^ Levin, Shulamit (January 2004). "Reversed Phase Stationary Phases in Pharmaceutical Sciences". Journal of Liquid Chromatography & Related Technologies. 27 (7–9): 1353–1376. doi:10.1081/JLC-120030606. ISSN 1082-6076. S2CID 97490509.
  3. ^ Gerber, F.; Krummen, M.; Potgeter, H.; Roth, A.; Siffrin, C.; Spoendlin, C. (2004). "Practical aspects of fast reversed-phase high-performance liquid chromatography using 3μm particle packed columns and monolithic columns in pharmaceutical development and production working under current good manufacturing practice". Journal of Chromatography A. 1036 (2): 127–133. doi:10.1016/j.chroma.2004.02.056. PMID 15146913.
  4. ^ Bayne, Shirley; Carlin, Michelle (2017). Forensic Applications of High Performance Liquid Chromatography (1st ed.). CRC Press. ISBN 9780429251962.
  5. ^ Seger, Christoph; Salzmann, Linda (2020-08-01). "After another decade: LC–MS/MS became routine in clinical diagnostics". Clinical Biochemistry. Advancement and Applications of Mass Spectrometry in Laboratory Medicine. 82: 2–11. doi:10.1016/j.clinbiochem.2020.03.004. ISSN 0009-9120. PMID 32188572. S2CID 213186669.

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