Liquid Crystalline Systems of Phytantriol and Glyceryl Monooleate Containing a Hydrophilic Protein: Characterisation, Swelling and Release Kinetics

被引:109
作者
Rizwan, S. B. [1 ]
Hanley, T. [3 ]
Boyd, B. J. [2 ]
Rades, T. [1 ]
Hook, S. [1 ]
机构
[1] Univ Otago, New Zealands Natl Sch Pharm, Dunedin, New Zealand
[2] Monash Univ, Monash Inst Pharmaceut Sci, Parkville, Vic 3052, Australia
[3] Australian Nucl Sci & Technol Org, Bragg Inst, Menai, NSW 2234, Australia
关键词
controlled release; diffusion; kinetics; lipids; protein delivery; LIPIDIC CUBIC PHASE; DRUG-RELEASE; BIOLOGICAL RELEVANCE; LIPOPHILIC COMPOUNDS; DELIVERY; BEHAVIOR; NANOPARTICLES; VESICLES; INSULIN; GELS;
D O I
10.1002/jps.21724
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Swelling and phase behaviour of phytantriol and glyceryl monooleate (GMO) matrices with varying water loadings were investigated. Release of a model protein, FITC-Ova was subsequently examined. Polarised light microscopy and small angle X-ray scattering analysis showed that the addition of FITC-Ova only altered the liquid crystalline structure of phytantriol matrices at low water loadings, and that postrelease study, the phase structure of matrices at both low and high loading reflected that of the binary system. Addition of FITC-Ova to GMO matrices also altered the liquid crystalline structure when compared to the respective binary system at low but not at high loading. All samples analysed after the release study had transformed to the reverse hexagonal phase (H-II). Swelling studies revealed a faster and more extensive swelling of GMO when compared to phytantriol. Release of FITC-Ova from phytantriol matrices was faster and occurred to a greater extent most likely due to the conversion of GMO matrices into the H-II phase. No effect on release as a function of initial water content was observed for either lipid. We have confirmed that phytantriol based liquid crystalline matrices can sustain the release of a hydrophilic protein, suggesting its suitability as a potential sustained antigen-delivery system. (C) 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 98:4191-4204, 2009
引用
收藏
页码:4191 / 4204
页数:14
相关论文
共 45 条
[31]   Physicochernical characterization of colloidal drug delivery systems such as reverse micelles, vesicles, liquid crystals and nanoparticles for topical administration [J].
Müller-Goymann, CC .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 58 (02) :343-356
[32]   Addition of hydrophilic and lipophilic compounds of biological relevance to the mnonoolein/water system II -: 13C NMR relaxation study [J].
Murgia, S ;
Caboi, F ;
Monduzzi, M .
CHEMISTRY AND PHYSICS OF LIPIDS, 2001, 110 (01) :11-17
[33]   A study of entrapped enzyme stability and substrate diffusion in a monoglyceride-based cubic liquid crystalline phase [J].
Nylander, T ;
Mattisson, C ;
Razumas, V ;
Miezis, Y ;
Hakansson, B .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1996, 114 :311-320
[34]  
Qui H, 2000, BIOMATERIALS, V21, P223
[35]  
RIBIER A, 1998, COSMETIC DERMATOLOGI
[36]   Characterisation of bicontinuous cubic liquid crystalline systems of phytantriol and water using cryo field emission scanning electron microscopy (cryo FESEM) [J].
Rizwan, S. B. ;
Dong, Y.-D. ;
Boyd, B. J. ;
Rades, T. ;
Hook, S. .
MICRON, 2007, 38 (05) :478-485
[38]   Stabilization of insulin against agitation-induced aggregation by the GMO cubic phase gel [J].
Sadhale, Y ;
Shah, JC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 191 (01) :51-64
[39]   Biological activity of insulin in GMO gels and the effect of agitation [J].
Sadhale, Y ;
Shah, JC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 191 (01) :65-74
[40]   KINETICS OF SWELLING OF POLYMERS AND THEIR GELS [J].
SCHOTT, H .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1992, 81 (05) :467-470