A structurally diverse library of safe-by-design citrem-phospholipid lamellar and non-lamellar liquid crystalline nano-assemblies

被引:68
|
作者
Azmi, Intan D. M. [1 ,2 ]
Wibroe, Peter P. [3 ]
Wu, Lin-Ping [3 ]
Kazem, Ali I. [1 ]
Amenitsch, Heinz [4 ]
Moghimi, Seyed M. [3 ,5 ,6 ]
Yaghmur, Anan [1 ]
机构
[1] Univ Copenhagen, Dept Pharm, Fac Hlth & Med Sci, Univ Pk 2, DK-2100 Copenhagen O, Denmark
[2] Univ Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor Darul, Malaysia
[3] Univ Copenhagen, Nanomed Lab, Ctr Pharmaceut Nanotechnol & Nanotoxicol, Dept Pharm,Fac Hlth & Med Sci, Univ Pk 2, DK-2100 Copenhagen O, Denmark
[4] Elettra Sincrotrone Trieste, Str Statale 14, I-34149 Trieste, Italy
[5] Univ Copenhagen, NanoSci Ctr, Univ Pk 2, DK-2100 Copenhagen O, Denmark
[6] Univ Durham, Sch Med Pharm & Hlth, Queens Campus, Stockton On Tees TS17 6BH, England
关键词
Complement system; Cubosomes; Hexosomes; Immune-safe nanopharmaceuticals; Lamellar and non-lamellar liquid crystalline phases; Macrophage; COMPLEMENT ACTIVATION; AQUEOUS DISPERSIONS; MEMBRANE-FUSION; PHOSPHATIDYLCHOLINE VESICLES; INTERNAL NANOSTRUCTURE; PHASE-TRANSITION; CUBIC PHASES; NANOPARTICLES; CUBOSOMES; OIL;
D O I
10.1016/j.jconrel.2016.08.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Non-lamellar liquid crystalline aqueous nanodispersions, known also as ISAsomes (internally self-assembled 'somes' or nanoparticles), are gaining increasing interest in drug solubilisation and bio-imaging, but they often exhibit poor hemocompatibility and induce cytotoxicity. This limits their applications in intravenous drug delivery and targeting. Using a binary mixture of citrem and soy phosphatidylcholine (SPC) at different weight ratios, we describe a library of colloidally stable aqueous and hemocompatible nanodispersions of diverse nanoarchitectures (internal self-assembled nanostructures). This engineered library is structurally stable in human plasma as well as being hemocompatible (non-hemolytic, and poor activator of the complement system). By varying citrem to lipid weight ratio, the nanodispersion susceptibility to macrophage uptake could also be modulated. Finally, the formation of nanodispersions comprising internally V-2 (inverse bicontinuous cubic) and H-2 (inverse hexagonal) nanoarchitectures was achieved without the use of an organic solvent, a secondary emulsifier, or high-energy input. The tunable binary citrem/SPC nanoplatform holds promise for future development of hemocompatible and immune-safe nanopharmaceuticals. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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