Layersome: Development and optimization of stable liposomes as drug delivery system

被引:45
作者
Ciobanu, M.
Heurtault, B.
Schultz, P.
Ruhlmann, C.
Muller, C. D.
Frisch, B.
机构
[1] Fac Pharm, CNRS ULP, LC01, UMR 7175, F-67400 Illkirch Graffenstaden, France
[2] CNRS INSERM ULP, IGBMC, F-67404 Illkirch Graffenstaden, France
关键词
stable liposomes; layersomes; coating; charged polymers;
D O I
10.1016/j.ijpharm.2007.05.037
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This paper describes the development of stable drug delivery systems named layersomes. The layersomes are conventional liposomes coated with one or multiple layers of biocompatible polyelectrolytes in order to stabilise their structure. The formulation strategy is based on an alternative coating procedure of positive poly(lysine) (pLL) and negative poly(glutamic acid) (pGA) polypeptides on initially charged small unilamellar liposomes (SUVs). The size distribution and the zeta potential of the final entity depend on the number of polyelectrolyte layers and the charge of the last coating layer. Morphological studies were achieved by flux cytometry and cryo electron microscopy. Release studies of encapsulated hydrophilic 5(6)-carboxyfluoreseein (5,6CF) in the presence of Triton (R) or ethanol showed an increased membrane resistance of the layersomes compared to classical SUVs. Finally, encapsulation of piroxicam (PX) was performed with success. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:154 / 157
页数:4
相关论文
共 21 条
[1]   Spectroscopic studies of micro environment dictated structural forms of piroxicam and meloxicam [J].
Banerjee, R ;
Sarkar, M .
JOURNAL OF LUMINESCENCE, 2002, 99 (03) :255-263
[2]   Liposil, a promising composite material for drug storage and release [J].
Begu, Sylvie ;
Pouessel, Anne Aubert ;
Lerner, Dan A. ;
Tourne-Peteilh, Corine ;
Devoisselle, Jean Marie .
JOURNAL OF CONTROLLED RELEASE, 2007, 118 (01) :1-6
[3]   Polyelectrolyte multilayer films with pegylated polypeptides as a new type of anti-microbial protection for biomaterials [J].
Boulmedais, F ;
Frisch, B ;
Etienne, O ;
Lavalle, P ;
Picart, C ;
Ogier, J ;
Voegel, JC ;
Schaaf, P ;
Egles, C .
BIOMATERIALS, 2004, 25 (11) :2003-2011
[4]   Fuzzy nanoassemblies: Toward layered polymeric multicomposites [J].
Decher, G .
SCIENCE, 1997, 277 (5330) :1232-1237
[5]   Biologically active lipid A antagonist embedded in a multilayered polyelectrolyte architecture [J].
Gangloff, SC ;
Ladam, G ;
Dupray, V ;
Fukase, K ;
Brandenburg, K ;
Guenounou, M ;
Schaaf, P ;
Voegel, JC ;
Jessel, N .
BIOMATERIALS, 2006, 27 (09) :1771-1777
[6]   Polymer-stabilized phospholipid vesicles formed on polyelectrolyte multilayer capsules [J].
Ge, LQ ;
Möhwald, H ;
Li, JB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (02) :653-659
[7]   Lipid-DNA complex formation: Reorganization and rupture of lipid vesicles in the presence of DNA as observed by cryoelectron microscopy [J].
Huebner, S ;
Battersby, BJ ;
Grimm, R ;
Cevc, G .
BIOPHYSICAL JOURNAL, 1999, 76 (06) :3158-3166
[8]   Stability of SUV liposomes in the presence of cholate salts and pancreatic lipases: effect of lipid composition [J].
Kokkona, M ;
Kallinteri, P ;
Fatouros, D ;
Antimisiaris, SG .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 9 (03) :245-252
[9]   Layer by layer self-assembled polyelectrolyte multilayers with embedded phospholipid vesicles [J].
Michel, M ;
Vautier, D ;
Voegel, JC ;
Schaaf, P ;
Ball, V .
LANGMUIR, 2004, 20 (12) :4835-4839
[10]   Comparison of polymerically stabilized PEG-grafted liposomes and physically adsorbed carboxymethylchitin and carboxymethyl/glycolchitin liposomes for biological applications [J].
Mobed, M ;
Chang, TMS .
BIOMATERIALS, 1998, 19 (13) :1167-1177