Quantitative studies of the autoxidation of linoleate monomers sequestered in phosphatidylcholine bilayers. Absolute rate constants in bilayers

• Published in: Canadian journal of chemistry 1985-10, Vol.63 (10), p.2633-2638
• Main Authors: Barclay, Lawrence Ross Coates, Locke, Steven Jeffrey, MacNeil, Joseph Mark, Vankessel, Joann
• Format: Article
• Language: English
• Subjects: Chemistry; Exact sciences and technology; Kinetics and mechanisms; Organic chemistry; Reactivity and mechanisms
• ISSN: 0008-4042; 1480-3291
• DOI: 10.1139/v85-437

The kinetics of autoxidation of linoleic acid in dimyristoylphosphatidylcholine (DMPC) bilayers were studied at 30 °C and pH 7 under 760 Torr O 2 . Reactions were initiated using either the lipid-soluble di-tert-butylhyponitrite (DBHN) or water-soluble azobis(2-amidinopropane)*HCl (ABAP). Rates of chain initiation, R i , were measured with a lipid-soluble antioxidant, a-tocopherol, or a water-soluble one, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylate (Trolox). The slightly higher oxidizability obtained compared to methyl linoleate in chlorobenzene is attributed to a moderate polar solvent effect on ionized linoleate near the bilayer surface. A low initiator efficiency, e = 0.0895 for DBHN in DMPC, is attributed to the cage effect in the bilayer of high microviscosity. Similar autoxidation experiments on methyl linoleate in DMPC bilayers gave a lower oxidizability , indicating that the ester is sequestered deeper in the hydrophobic region of DMPC than is ionized linoleate. Some absolute rate constants are determined using the rotating sector technique for linoleic acid in 0.50 M SDS micelles, and egg lecithin and dilinoleoylphosphatidylcholine (DLPC) bilayers. A hundredfold decrease in the termination rate constant, 2k t for DLPC bilayer compared to homogeneous solution is attributed to chain termination in a bilayer region of high polarity. A concomitant reduction (up to tenfold) in the propagation rate constant, k p , is attributed to diffusion of polar peroxyl radicals away from the oxidizable region of the bilayer.