Epidermal growth factor receptor-targeted lipid nanoparticles retain self-assembled nanostructures and provide high specificity

被引:67
|
作者
Zhai, Jiali [1 ]
Scoble, Judith A. [2 ]
Li, Nan [1 ,5 ]
Lovrecz, George [1 ]
Waddington, Lynne J. [2 ]
Tran, Nhiem [1 ]
Muir, Benjamin W. [1 ]
Coia, Gregory [2 ]
Kirby, Nigel [3 ]
Drummond, Calum J. [4 ]
Mulet, Xavier [1 ]
机构
[1] CSIRO Mfg Flagship, Clayton, Vic 3169, Australia
[2] CSIRO Mfg Flagship, Parkville, Vic 3052, Australia
[3] Australian Synchrotron, Clayton, Vic 3168, Australia
[4] RMIT Univ, Coll Sci Engn & Hlth, Sch Appl Sci, Melbourne, Vic 3001, Australia
[5] Tongji Univ, Sch Med, Shanghai Pulm Hosp, Dept Resp Med, Shanghai 200433, Peoples R China
关键词
LIQUID-CRYSTALLINE PARTICLES; DRUG DELIVERY-SYSTEMS; X-RAY-SCATTERING; ANTI-HER2; IMMUNOLIPOSOMES; PHASE-BEHAVIOR; ORAL DELIVERY; CUBIC PHASES; IN-VITRO; PHYTANTRIOL; ANTIBODY;
D O I
10.1039/c4nr05200e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Next generation drug delivery utilising nanoparticles incorporates active targeting to specific sites. In this work, we combined targeting with the inherent advantages of self-assembled lipid nanoparticles containing internal nano-structures. Epidermal growth factor receptor (EGFR)-targeting, PEGylated lipid nanoparticles using phytantriol and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-PEG-maleimide amphiphiles were created. The self-assembled lipid nanoparticles presented here have internal lyotropic liquid crystalline nano-structures, verified by synchrotron small angle X-ray scattering and cryo-transmission electron microscopy, that offer the potential of high drug loading and enhanced cell penetration. Anti-EGFR Fab' fragments were conjugated to the surface of nanoparticles via a maleimide-thiol reaction at a high conjugation efficiency and retained specificity following conjugation to the nanoparticles. The conjugated nanoparticles were demonstrated to have high affinity for an EGFR target in a ligand binding assay.
引用
收藏
页码:2905 / 2913
页数:9
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