Title: Sticky Patches on Lipid Nanoparticles Enable the Selective Targeting and Killing of Untargetable Cancer Cells
Authors: SEMPKOWSKI MichelleZHU CharlesMENZENSKI MonikaKEVREKIDIS Ioannis G.BRUCHERTSEIFER FrankMORGENSTERN AlfredSOFOU Stavroula
Citation: MOLECULAR CANCER THERAPEUTICS vol. 32 no. 33 p. 8329-8338
Publisher: AMER ASSOC CANCER RESEARCH
Publication Year: 2016
JRC N°: JRC99551
ISSN: 1535-7163
URI: http://publications.jrc.ec.europa.eu/repository/handle/JRC99551
DOI: 10.1021/acs.langmuir.6b01464
Type: Articles in periodicals and books
Abstract: Effective targeting by uniformly functionalized nanoparticles is limited to cancer cells expressing at least two copies of targeted receptors per nanoparticle footprint (approximately ≥2 × 105 receptor copies per cell); such a receptor density supports the required multivalent interaction between the neighboring receptors and the ligands from a single nanoparticle. To enable selective targeting below this receptor density, ligands on the surface of lipid vesicles were displayed in clusters that were designed to form at the acidic pH of the tumor interstitium. Vesicles with clustered HER2-targeting peptides within such sticky patches (sticky vesicles) were compared to uniformly functionalized vesicles. On HER2-negative breast cancer cells MDA-MB-231 and MCF7 {expressing (8.3 ± 0.8) × 104 and (5.4 ± 0.9) × 104 HER2 copies per cell, respectively}, only the sticky vesicles exhibited detectable specific targeting (KD ≈ 49–69 nM); dissociation (0.005–0.009 min–1) and endocytosis rates (0.024–0.026 min–1) were independent of HER2 expression for these cells. MDA-MB-231 and MCF7 were killed only by sticky vesicles encapsulating doxorubicin (32–40% viability) or α-particle emitter 225Ac (39–58% viability) and were not affected by uniformly functionalized vesicles (>80% viability). Toxicities on cardiomyocytes and normal breast cells (expressing HER2 at considerably lower but not insignificant levels) were not observed, suggesting the potential of tunable clustered ligand display for the selective killing of cancer cells with low receptor densities.
JRC Directorate:Nuclear Safety and Security

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