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A laboratory instrument which develops centrifugal fields of more than 100,000 times gravity, used for the quantitative measurement of sedimentation velocity or sedimentation equilibrium, or for the separation of solutes in liquid solutions to study high polymers, particularly proteins, nucleic acids, viruses, and other macromolecules of biological origin.



a device for separating particles less than 100 nanometers in size, such as colloids, subcellular particles, and macromolecules of proteins, nucleic acids, lipids, polysaccharides, and synthetic polymers, which are suspended or dissolved in a liquid. This is achieved by the rapid rotation of a rotor, which creates a centrifugal field with an acceleration many orders greater than the acceleration of gravity.

Ultracentrifuges are classified as preparative, analytical, or preparative-analytical according to their purpose and design.

Preparative ultracentrifuges are equipped with fixed-angle rotors, which have recesses for test tubes, beakers, or bottles, tilted at an angle of 20°-40° to the vertical axis of the rotor. Some have swinging-bucket rotors, with beakers that tilt 90° upon rotation. There are also ultracentrifuges with zonal or continuous-action rotors, with a single large vessel for the liquid being fractionated. Preparative ultracentrifuges are used to isolate individual components from complex mixtures.

Analytical ultracentrifuges have rotors with through-cylindrical recesses, in which special transparent vessels are inserted for the solutions or suspensions to be analyzed. The redistribution of particles in the solutions and suspensions may be observed directly during rotor rotation with the aid of special optical systems, such as refractometric or absorption devices. Some analytical ultracentrifuges are connected to electronic computers, which carry out the automatic processing of experimental data.

The first ultracentrifuge, designed for studying the motion of particles invisible under a microscope, was constructed by the Swedish scientist T. Svedberg in 1923 (discovery announced in 1924). This ultracentrifuge, in which a centrifugal force of up to 5,000 g was achieved, had an absorption optical system and was used to study the motion of gold particles with a diameter of approximately 5 nanometers. In 1926, Svedberg built the first highspeed ultracentrifuge (41,000 rpm, acceleration up to 105 g), which made possible the analytical study of proteins in solutions, particularly the study of hemoglobin. In 1939 he designed an analytical ultracentrifuge with a steel rotor (65,000 rpm).

The vast majority of modern laboratory ultracentrifuges are electrically driven and have aluminum or titanium rotors. In the USSR and abroad many types of ultracentrifuges are being produced in which accelerations of up to 500,000 g are created, and the separation of particles and molecules is carried out in volumes measuring tens and hundreds of milliliters.


Lotts, Iu. A., and A. Ia. Ozherel’ev. “Analiticheskaia ul’tratsentrifuga.” Unikal’nyepribory, 1970, no. 5.
Svedberg, T, and K. O. Pedersen. The Ultracentrifuge. Oxford, 1940.


References in periodicals archive ?
By use of a gradient tube of a swing-out rotor, the gradient is constructed by consecutive layering of 4 salt solutions of distinct densities that have been adjusted accurately at the same temperature as that of the ultracentrifugal separation (+15[degrees] C).
Richard Havel developed an ultracentrifugal method in 1955 that continues to be the common citation for preparative isolation of the lipoproteins (2).
b) Fractions with apparently incomplete ultracentrifugal separation or no elution peak because low cholesterol concentration observed in their HPLC patterns were excluded.
Ratio of remnant-like particle-cholesterol to serum total triglycerides is an effective alternative to ultracentrifugal and electrophoretic methods in the diagnosis of familial type III hyperlipoproteinemia.
Ultracentrifugal studies of high-density serum lipoproteins in clinically healthy adults.
When the HDLZ ultracentrifugal subfraction of plasma was reacted with purified phosphatidyl transfer protein, Sm LpA-I particles of ~45 kDa were generated that could be detected using Superose 6 HP-SEC (84).
006 kg/L, apolipoprotein B-containing lipoproteins in the ultracentrifugal infranate are precipitated with heparin and Mn[Cl.