STRUCTURAL REQUIREMENTS OF STEROLS FOR INTERACTION WITH LECITHIN AT AIR-WATER INTERFACE
STRUCTURAL REQUIREMENTS OF STEROLS FOR INTERACTION WITH LECITHIN AT AIR-WATER INTERFACE
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DOI:
10.1016/0005-2736(72)90030-2
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发表时间:
1972-01-01
期刊:
影响因子:
--
通讯作者:
BRUCKDORFER, KR
中科院分区:
文献类型:
--
作者:
DEMEL, RA;VANDEENE.LL;BRUCKDORFER, KR
1.1. The force area characteristics of monolayers of 3β-, 3α-hydroxysterols and ketosteroids have been studied.2.2. The 3β-hydroxysterols cholesterol, cholestanol, lathosterol, 7-dehydrocholesterol, and B-norcholesterol are perpendicularly oriented at the air-water interface and show high collapse pressures. Ergosterol, stigmasterol, and androstan-3β-ol demonstrate a similar behavior at high pressures, but the collapse pressure is reduced. Thecis-structured coprostanol shows an increased area per molecule. 3α-Hydroxysterols (epicholesterol and androstan-3α-ol) reveal strongly reduced collapse pressures when compared with the respective 3β-hydroxysterols. All ketosteroids show high areas per molecule.3.3. The force-area curves show little temperature effect.4.4. The interaction of 18:1/18:0 lecithin with sterols is dependent on: (a) planar sterol nucleus, (b) 3β-hydroxy group, (c) intact side chain.5.5. Besides 3β-hydroxysterols, 3α-hydroxysterols and ketosteroids can also show some condensation effect. However, minimal area per molecule can be achieved only with 3β-hydroxysterols.6.6. The interaction of lecithin and sterol in monolayers is governed by a number of factors including van der Waal's interactions, but also hydrogen bonding between the 3β-hydroxy group and environment is considered to be important.