Behavior of specific natural lecithins and cholesterol at the air water-interface
β Scribed by Dolly Ghosh; Richard L. Lyman; J. Tinoco
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- English
- Weight
- 460 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0009-3084
No coin nor oath required. For personal study only.
β¦ Synopsis
Individual molecular species of lecithins were mixed with cholesterol and their pressurearea curves were measured at the air-water interface at 22 _~ 1". The lecithins investigated were*: L-16:0-16:0-, D-16:0-16:0-, L-16:0-18:3-, L-18:0-18:3-, L-16:0-20:4-, L-18:0-20:4-and L-18:0-18:0-1ecithins. All of these except the D-16:0-16:0-and L-18:0-18:0lecithins have been found in nature. Considerable condensation of monolayers with cholesterol was observed in all cases except that of 18:0-18:0-lecithin, in which there was little condensation. The naturally-occurring structure of lecithins, that is, 1-saturated-2-unsaturated, leads to large condensations in mixed monolayers. This geometrical fit between cholesterol and lecithins may be of importance in enzyme reactions involving cholesterol or lecithins. * Abbreviations: Fatty acids -number of carbon atoms: number of double bonds; Lecithins -substituent in position 1 named first, substituent in position 2 named second. For example, 16: 0-18 : 3-lecithin --1-palmitoyl-2-1inolenoyl lecithin.
π SIMILAR VOLUMES
The oxidation of cholesterol and the behavior of an oxidized sterol, 5-a-hydroperoxycholesterol (5-AHC), have been investigated. It is demonstrated that previous work is correct in observing that cholesterol oxidation does take place at the air/water interface, but predicts initial effects and rates
Literature data for homologous series of nonionic and ionic surfactants, such as C(n)OH, C(n)EO(m), Tritons, C(n)SO4Na, and C(n)EO(m)SO4Na, were analyzed on the basis of the Frumkin and reorientation models. The thermodynamic quantities obtained from the reorientation model agree best with the exper