MICELLE FORMATION OF N-DECANOYLGLYCINE AND N-DECANOYL-L-ALANINE OLIGOMER POTASSIUM-SALTS AND THE MICELLAR STRUCTURE - A SMALL-ANGLE NEUTRON-SCATTERING STUDY

Citation
H. Etori et al., MICELLE FORMATION OF N-DECANOYLGLYCINE AND N-DECANOYL-L-ALANINE OLIGOMER POTASSIUM-SALTS AND THE MICELLAR STRUCTURE - A SMALL-ANGLE NEUTRON-SCATTERING STUDY, Colloid and polymer science, 275(3), 1997, pp. 263-273
Citations number
34
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
0303402X
Volume
275
Issue
3
Year of publication
1997
Pages
263 - 273
Database
ISI
SICI code
0303-402X(1997)275:3<263:MFONAN>2.0.ZU;2-O
Abstract
Potassium salts of N-decanoylglycine and N-decanoyl-L-alanine oligopep tides (monomer, dimer and trimer) were synthesized. For these oligomer salts in aqueous solutions, the microstructures of micelles have been investigated by small-angle neutron-scattering (SANS). In the calcula tion of SANS intensity data, the thickness of the hydrophilic layer wa s altered by changing the conformation of the oligomer moiety (helical and beta-sheet structures). For micelles of the trimer salts, the hel ical structure models provide the best fit to the observed SANS intens ity data. For micelles of the monomer- and dimer-salts, the beta-sheet model provides the best fit to the observed data. For the monomer- an d dimer-micelles, the aggregation number (n) is not dependent on the s pecies of amino acid residue, implying that the decanoyl group plays a critical role in micelle formation. However, for the trimer micelles, the n value is dependent on the species of amino acid residue.