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.
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Univ Illinois, Coll Med, Dept Med, Div Hematol Oncol, Chicago, IL USAUniv Illinois, Coll Med, Dept Med, Div Hematol Oncol, Chicago, IL USA
Moreira, Jonathan
Tobias, Alexander
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Rosalind Franklin Univ Med & Sci, N Chicago, IL USAUniv Illinois, Coll Med, Dept Med, Div Hematol Oncol, Chicago, IL USA
Tobias, Alexander
O'Brien, Michael P.
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Loyola Univ, Chicago, IL 60611 USAUniv Illinois, Coll Med, Dept Med, Div Hematol Oncol, Chicago, IL USA
O'Brien, Michael P.
Agulnik, Mark
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Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Div Hematol Oncol, 676 N St Clair St,Suite 850, Chicago, IL 60611 USAUniv Illinois, Coll Med, Dept Med, Div Hematol Oncol, Chicago, IL USA