T. Viitala et al., SYNTHESIS AND LANGMUIR FILM FORMATION OF N-(EPSILON-MALEIMIDOCAPROYL)(DILINOLEOYLPHOSPHATIDYL) ETHANOLAMINE, Langmuir, 14(5), 1998, pp. 1272-1277
imidocaproyl)(dilinoleoylphosphatidyl)ethanolamine (DLiPE-EMC) has bee
n synthesized, representing a new polymerizable lipid with a linking g
roup for covalent attachment of proteins for immunosensor applications
. The linker lipid could be prepared by performing both the synthesis
and separation steps under argon and avoiding heating. The product was
characterized by 600 MHz H-1 NMR, mass, and UV-vis spectrometry. Mono
molecular films were successfully prepared on a Langmuir trough, and t
he characteristic surface pressure-area curves were measured on differ
ent subphases, A condensation of the monolayer could be achieved by in
troducing a micromolar concentration of uranyl ions in the subphase. S
urface pressure-area isotherms of pure and mixed DLiPE/DLiPE-EMC monol
ayers were also measured. UV irradiation experiments were performed to
demonstrate the polymerizability of the mixed monolayers.