[Gas chromatographic determination of vitamin F and vitamin E in combination with vitamin A and with various components in pharmaceutical preparations]. 1969

M Feroci, and G Orzalesi, and R Selleri

UI MeSH Term Description Entries
D008722 Methods A series of steps taken in order to conduct research. Techniques,Methodological Studies,Methodological Study,Procedures,Studies, Methodological,Study, Methodological,Method,Procedure,Technique
D002626 Chemistry, Pharmaceutical Chemistry dealing with the composition and preparation of agents having PHARMACOLOGIC ACTIONS or diagnostic use. Medicinal Chemistry,Chemistry, Pharmaceutic,Pharmaceutic Chemistry,Pharmaceutical Chemistry,Chemistry, Medicinal
D002849 Chromatography, Gas Fractionation of a vaporized sample as a consequence of partition between a mobile gaseous phase and a stationary phase held in a column. Two types are gas-solid chromatography, where the fixed phase is a solid, and gas-liquid, in which the stationary phase is a nonvolatile liquid supported on an inert solid matrix. Chromatography, Gas-Liquid,Gas Chromatography,Chromatographies, Gas,Chromatographies, Gas-Liquid,Chromatography, Gas Liquid,Gas Chromatographies,Gas-Liquid Chromatographies,Gas-Liquid Chromatography
D005228 Fatty Acids, Essential Long chain organic acid molecules that must be obtained from the diet. Examples are LINOLEIC ACIDS and LINOLENIC ACIDS. Acids, Essential Fatty,Essential Fatty Acids
D014801 Vitamin A Retinol and derivatives of retinol that play an essential role in metabolic functioning of the retina, the growth of and differentiation of epithelial tissue, the growth of bone, reproduction, and the immune response. Dietary vitamin A is derived from a variety of CAROTENOIDS found in plants. It is enriched in the liver, egg yolks, and the fat component of dairy products. Retinol,11-cis-Retinol,3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, (all-E)-Isomer,All-Trans-Retinol,Aquasol A,Vitamin A1,All Trans Retinol
D014810 Vitamin E A generic descriptor for all TOCOPHEROLS and TOCOTRIENOLS that exhibit ALPHA-TOCOPHEROL activity. By virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus, these compounds exhibit varying degree of antioxidant activity, depending on the site and number of methyl groups and the type of ISOPRENOIDS.

Related Publications

M Feroci, and G Orzalesi, and R Selleri
February 1970, Journal of pharmaceutical sciences,
M Feroci, and G Orzalesi, and R Selleri
October 1972, Journal of chromatography,
M Feroci, and G Orzalesi, and R Selleri
December 1967, The Journal of pharmacy and pharmacology,
M Feroci, and G Orzalesi, and R Selleri
January 1986, Journal - Association of Official Analytical Chemists,
M Feroci, and G Orzalesi, and R Selleri
September 1966, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
M Feroci, and G Orzalesi, and R Selleri
April 1984, Journal of chromatography,
M Feroci, and G Orzalesi, and R Selleri
May 1970, Bollettino chimico farmaceutico,
M Feroci, and G Orzalesi, and R Selleri
September 1969, Bollettino chimico farmaceutico,
M Feroci, and G Orzalesi, and R Selleri
June 1966, Acta pharmaceutica Suecica,
M Feroci, and G Orzalesi, and R Selleri
January 1976, Journal of nutritional science and vitaminology,
Copied contents to your clipboard!