Preparation of liposomes containing small gold nanoparticles using electrostatic interactions

被引:28
作者
Dichello, Gennaro A. [1 ]
Fukuda, Takahiro [4 ]
Maekawa, Toni [4 ]
Whitby, Raymond L. D. [1 ,2 ]
Mikhalovsky, Sergey V. [1 ,2 ]
Alavijeh, Mohammed [3 ]
Pannala, Ananth S. [1 ]
Sarker, Dipak K. [1 ]
机构
[1] Univ Brighton, Sch Pharm & Biomol Sci, Biomat & Drug Delivery Res Grp, Brighton BN2 4GJ, E Sussex, England
[2] Nazarbayev Univ, Fac Engn, Dept Chem Engn, 53 Kabanbay Batyr Ave, Astana, Kazakhstan
[3] Pharmidex, 14 Hanover St, London W1S 1YH, England
[4] Toyo Univ, Bionano Elect Res Ctr, Kawagoe, Saitama, Japan
基金
英国医学研究理事会;
关键词
Nanopartide; Liposome; Encapsulation; Electrostatic interaction; Loading content; DRUG; SIZE; ENCAPSULATION; DEPENDENCE; EFFICIENCY; SHAPE;
D O I
10.1016/j.ejps.2017.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The development of liposome-nanoparticle colloid systems offers a versatile approach towards the manufacture of multifunctional therapeutic platforms. A strategy to encapsulate small metallic nanoparticles (< 4 nm) within multilamellar vesicles, effected by exploiting electrostatic interactions was investigated. Two liposome-gold nanoparticle (lipo-GNP) systems were prepared by the reverse-phase evaporation method employing cationic or anionic surface functionalised particles in combination with oppositely charged lipid compositions with subsequent post-formulation PEGylation. Structural characterisation using electron microscopy and elemental analysis revealed a regular distribution of GNPs between adjacent lipid bilayers of intact liposomes. Nanoparticle encapsulation efficacy of the two lipo-GNP systems was revealed to be significantly different (p = 0.03), evaluated by comparing the ratio of measured lipid to gold concentration (loading content) determined by a colorimetric assay and atomic emission spectroscopy, respectively. It was concluded that the developed synthetic strategy is an effective approach for the preparation of liposome-nanoparticle colloids with potential to control the relative concentration of encapsulated particles to lipids by providing favourable electrostatic interactions.
引用
收藏
页码:55 / 63
页数:9
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