326
Views
3
CrossRef citations to date
0
Altmetric
Original Articles

Relationship between liquid crystalline phase stability and ingredient composition in liquid crystal oil–water emulsion

, , , , , , & show all
Pages 1495-1502 | Received 19 Feb 2016, Accepted 28 Apr 2016, Published online: 17 May 2016

References

  • Friberg S. Liquid crystalline phases in emulsions. J Colloid Interface Sci. 1971;37:291–295. doi:10.1016/0021-9797(71)90295-5.
  • Suzuki T, Tsutsumi H, Ishida A. Secondary droplet emulsion: mechanism and effects of liquid crystal formation in o/w emulsion. J Dispers Sci Technol. 1984;5:119–141. doi:10.1080/01932698408943213.
  • Suzuki T, Takei H, Yamazaki S. Formation of fine three-phase emulsions by the liquid crystal emulsification method with arginine β-branched monoalkyl phosphate. J Colloid Interface Sci. 1989;129:491–500. doi:10.1016/0021-9797(89)90463-3.
  • Friberg SE. Micelles, microemulsions, liquid crystals, and the structure of stratum corneum lipids. J Soc Cosmet Chem. 1990;41:155–171.
  • Iwai H, Fukasawa J, Suzuki T. A liquid crystal application in skin care cosmetics. Int J Cosmet Sci. 1998;20:87–102. doi:10.1046/j.1467-2494.1998.171741.x.
  • Liu Y, Friberg SE. Role of liquid crystal in the emulsification of a gel emulsion with high internal phase fraction. J Colloid Interface Sci. 2009;340:261–268. doi:10.1016/j.jcis.2009.08.038.
  • Vilasau J, Solans C, Gómez M, et al. Phase behaviour of a mixed ionic/nonionic surfactant system used to prepare stable oil-in-water paraffin emulsions. Colloids Surf A Physicochem Eng Asp. 2011;384:473–481. doi:10.1016/j.colsurfa.2011.05.029.
  • Nesseem DI. Formulation and evaluation of itraconazole via liquid crystal for topical delivery system. J Pharm Biomed Anal. 2001;26:387–399. doi:10.1016/S0731-7085(01)00414-9.
  • Müller-Goymann C. Physicochemical characterization of colloidal drug delivery systems such as reverse micelles, vesicles, liquid crystals and nanoparticles for topical administration. Eur J Pharm Biopharm. 2004;58:343–356. doi:10.1016/j.ejpb.2004.03.028.
  • Toquer G, Phou T, Monge S, et al. Colloidal shape controlled by molecular adsorption at liquid crystal interfaces. J Phys Chem B. 2008;112:4157–4160. doi:10.1021/jp800431y.
  • Otto A, Du Plessis J, Wiechers J. Formulation effects of topical emulsions on transdermal and dermal delivery. Int J Cosmet Sci. 2009;31:1–19. doi:10.1111/ics.2008.31.issue-1.
  • Hosmer JM, Steiner AA, Lopes LB. Lamellar liquid crystalline phases for cutaneous delivery of paclitaxel: impact of the monoglyceride. Pharm Res. 2013;30:694–706. doi:10.1007/s11095-012-0908-0.
  • Bouwstra J, Gooris G, Dubbelaar F, et al. pH, cholesterol sulfate, and fatty acids affect the stratum corneum lipid organization. J Investig Dermatol Symp Proc. 1998;3:69–74. doi:10.1038/jidsymp.1998.17.
  • Bouwstra JA, Gooris GS, Dubbelaar FER, et al. Phase behavior of stratum corneum lipid mixtures based on human ceramides: the role of natural and synthetic ceramide 1. J Investig Dermatol. 2002;118:606–617. doi:10.1046/j.1523-1747.2002.01706.x.
  • Zhang W, Zhu L. Study on the influence of emulsion technology on the formation of liquid crystal structural. China Surfactant Deterg. 2009;Issue 1:35–38.
  • Zhang W, Liu L. Influence of other ingredients on the formation of liquid crystal in APG system. China Surfactant Deterg. 2010;Issue 1:35–39.
  • Sonoda T, Takata Y, Ueno S, et al. Effects of emulsifiers on crystallization behavior of lipid crystals in nanometer-size oil-in-water emulsion droplets. Cryst Growth Des. 2006;6:306–312. doi:10.1021/cg050045h.
  • Saulnier P, Anton N, Heurtault B, et al. Liquid crystals and emulsions in the formulation of drug carriers. Comptes Rendus Chimie. 2008;11:221–228. doi:10.1016/j.crci.2007.10.005.
  • Alam MM, Aramaki K. Effect of molecular weight of triglycerides on the formation and rheological behavior of cubic and hexagonal phase based gel emulsions. J Colloid Interface Sci. 2009;336:329–334. doi:10.1016/j.jcis.2009.03.054.
  • Zhang W, Liu L. Study on the formation and properties of liquid crystal emulsion in cosmetic. J Cosmet Dermatol Sci Appl. 2013;3:139–144. doi:10.4236/jcdsa.2013.32022.
  • Dong YD, Boyd BJ. Applications of X-ray scattering in pharmaceutical science. Int J Pharm. 2011;417:101–111. doi:10.1016/j.ijpharm.2011.01.022.
  • Mao L, Calligaris S, Barba L, et al. Monoglyceride self-assembled structure in O/W emulsion: formation, characterization and its effect on emulsion properties. Food Res Int. 2014;58:81–88. doi:10.1016/j.foodres.2014.01.042.
  • Lee JB, Lee DR, Choi NC, et al. Efficient dermal delivery of retinyl palmitate: progressive polarimetry and Raman spectroscopy to evaluate the structure and efficacy. Eur J Pharm Sci. 2015;78:111–120. doi:10.1016/j.ejps.2015.07.009.
  • Kitzerow H-S. Polymer-dispersed liquid crystals from the nematic curvilinear aligned phase to ferroelectric films. Liq Cryst. 1994;16:1–31. doi:10.1080/02678299408036517.
  • Pezzaniti JL, Chipman RA. Mueller matrix imaging polarimetry. Opt Eng. 1995;34:1558–1568. doi:10.1117/12.206161.
  • Chipman RA. Handbook of optics. New York (NY): McGraw Hill; 1995. Chapter 22, Polarimetry; p. 22.1–22.37.
  • Lu SY, Chipman RA. Interpretation of Mueller matrices based on polar decomposition. J Opt Soc Am A. 1996;13:1106–1113. doi:10.1364/JOSAA.13.001106.
  • Prost J, de Gennes PG. The physics of liquid crystals. 2nd ed. Clarendon: Oxford University Press; 1995.
  • Israelachvili JN, Mitchell DJ, Ninham BW. Theory of self-assembly of hydrocarbon amphiphiles into micelles and bilayers. J Chem Soc Faraday Trans 2: Mol Chem Phys. 1976;72:1525–1568. doi:10.1039/f29767201525.
  • Kimura H. Nematic ordering of rod-like molecules interacting via anisotropic dispersion forces as well as rigid-body repulsions. J Phys Soc Japan. 1974;36:1280–1287. doi:10.1143/JPSJ.36.1280.
  • Yoon G, Park JW, Yoon I-S. Solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs): recent advances in drug delivery. J Pharm Investig. 2013;43:353–362. doi:10.1007/s40005-013-0087-y.
  • Weber S, Zimmer A, Pardeike J. Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) for pulmonary application: a review of the state of the art. Eur J Pharm Biopharm. 2014;86:7–22. doi:10.1016/j.ejpb.2013.08.013.
  • Natarajan JV, Nugraha C, Ng XW, et al. Sustained-release from nanocarriers: a review. J Control Release. 2014;193:122–138. doi:10.1016/j.jconrel.2014.05.029.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.