journal article·2003-10-01

Nonlamellar Liquid Crystalline Phases and Their Particle Formation in the Egg Yolk Phosphatidylcholine/Diolein System

Tomoari Kamo, Minoru Nakano, Warunee Leesajakul, Atsuhiko Sugita, Hideki Matsuoka, Tetsurou Handa

Langmuir· Volume 19· Issue 22
Publisher page

Abstract

The phase behavior of fully hydrated egg yolk phosphatidylcholine (EPC)/diolein (DO) mixtures was investigated by small-angle X-ray scattering and 31 P NMR. EPC formed a lamellar phase, whereas DO gave a negative curvature to the lipid membranes, leading to nonlamellar phase formation. At an EPC/DO molar ratio of 8:2, the mixture formed a bicontinuous cubic phase of primitive type. A bicontinuous cubic phase of diamond type was also observed at the ratio of 7:3, but it coexisted with an inverted hexagonal (H II ) phase. The mixture with higher DO fractions formed the H II phase. We further investigated if these nonlamellar phases could be dispersed by high-pressure emulsification with Pluronic F127, to form cubosomes or hexosomes, as have been obtained in monoolein-based cubic and H II phases ( Langmuir 2001, 17, 3917−3922; Langmuir 2002, 18, 9283−9288). As a result, cubosomes could not be obtained and vesicles were formed instead, presumably due to the existence of F127, which gave a positive curvature to the negatively curved membranes. However, the H II phase, which was less compatible with F127, could be dispersed to form hexosomes.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Lipid Membrane Structure and Behavior · Proteins in Food Systems · Surfactants and Colloidal Systems

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan, and Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan

References (32)

Show source-provided references
1. Pelech S. · Trans. Biochem. Soc. · 1989 · 14 · 30
2. Nishizuka Y. · Nature · 1984 · 308 · 69810.1038/308693a0 ↗
3. Bell R. M. · Cell · 1986 · 45 · 632
4. Dawson R. M. C. · Biochem. Biophys. Res. Commun. · 1983 · 117 · 201
5. Dawson R. M. C. · J. Biochem. Biophys. Res. Commun. · 1984 · 125 · 842
6. Siegel D. · Biochemistry · 1989 · 28 · 3709
7. Bezrukov S. M. · Curr. Opin. Colloid Interface Sci. · 2000 · 5 · 24310.1016/S1359-0294(00)00061-3 ↗
8. Takahashi H. · Biophys. J. · 1996 · 70 · 141110.1016/S0006-3495(96)79699-6 ↗
9. Leikin S. · Biophys. J. · 1996 · 71 · 263210.1016/S0006-3495(96)79454-7 ↗
10. Semmler K. · J. Chem. Phys. Lipids · 1999 · 99 · 16710.1016/S0009-3084(99)00038-9 ↗
11. Seddon J. M. · Biochemistry · 1990 · 29 · 800210.1021/bi00486a031 ↗
12. Oradd G. · Biophys. J. · 1995 · 68 · 1863
13. Nakano M. · Langmuir · 2001 · 17 · 392210.1021/la010224a ↗
14. Nakano M. · Langmuir · 2002 · 18 · 9288
15. Thumser A. E. A. · J. Lipid Res. · 1998 · 39 · 1038
16. Duff S. M. · J. Nutr. · 2001 · 131 · 778
17. Brecher P. · J. Biol. Chem. · 1984 · 259 · 1340110.1016/S0021-9258(18)90708-8 ↗
18. Garstecki P. · Langmuir · 2002 · 18 · 2528
19. Garstecki P. · Langmuir · 2002 · 18 · 2537
20. Saito H. · Langmuir · 1995 · 11 · 3747
21. Larsson K. · J. Phys. Chem. · 1989 · 93 · 7314
22. Razumas V. · J. Phys. Chem. · 1996 · 100 · 1177410.1021/jp952613h ↗
23. Razumas V. · Chem. Phys. Lipids · 1996 · 84 · 13810.1016/S0009-3084(96)02629-1 ↗
24. Barauskas J. · Chem. Phys. Lipids · 1999 · 97 · 17910.1016/S0009-3084(98)00107-8 ↗
25. Engström S. · Eur. J. Pharm. Sci. · 1999 · 8 · 25410.1016/S0928-0987(99)00012-3 ↗
26. Borne J. · Langmuir · 2000 · 16 · 1005410.1021/la000619e ↗
27. Caboi F. · Chem. Phys. Lipids · 2001 · 109 · 6210.1016/S0009-3084(00)00200-0 ↗
28. Borne J. · Langmuir · 2001 · 17 · 775110.1021/la010650w ↗
29. Hyde S. T. · Z. Kristallogr. · 1984 · 168 · 219
30. Gustafsson J. · Langmuir · 1996 · 12 · 461310.1021/la960318y ↗
31. Gustafsson J. · Langmuir · 1997 · 13 · 6971
32. Winter R. · Phys. Chem. Chem. Phys. · 1999 · 1 · 89310.1039/a808950g ↗