Tumor-specific targeting of polymer drug delivery systems with recombinant proteins bound via tris(nitrilotriacetic acid)

[Display omitted] •HPMA- and NIPMAM-based polymers are suitable nanocarriers for Ab delivery.•His-tagged Ab fragment forms well-defined complexes with trisNTA-polymer conjugates.•Polymers targeted with scFv-GD2 Ab fragments specifically bind to GD2 positive cells.•Polymer/Ab complexes can induce cel...

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Veröffentlicht in:International journal of pharmaceutics 2023-12, Vol.648, p.123619-123619, Article 123619
Hauptverfasser: Pechar, Michal, Král, Vlastimil, Kracíková, Lucie, Androvič, Ladislav, Hrdá, Eliška, Pola, Robert, Pytlíková, Sára, Studenovský, Martin, Kostka, Libor, Šubr, Vladimír, Etrych, Tomáš, Kočková, Olga, Marianne Ferreira Mendes, Jessica, Fábry, Milan, Laga, Richard
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Sprache:eng
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Zusammenfassung:[Display omitted] •HPMA- and NIPMAM-based polymers are suitable nanocarriers for Ab delivery.•His-tagged Ab fragment forms well-defined complexes with trisNTA-polymer conjugates.•Polymers targeted with scFv-GD2 Ab fragments specifically bind to GD2 positive cells.•Polymer/Ab complexes can induce cell death by cross-linking their surface receptors. Antibody-mediated targeting is an efficient strategy to enhance the specificity and selectivity of polymer nanomedicines towards the target site, typically a tumor. However, direct covalent coupling of an antibody with a polymer usually results in a partial damage of the antibody binding site accompanied with a compromised biological activity. Here, an original solution based on well-defined non-covalent interactions between tris-nitrilotriacetic acid (trisNTA) and hexahistidine (His-tag) groups, purposefully introduced to the structure of each macromolecule, is described. Specifically, trisNTA groups were attached along the chains of a hydrophilic statistical copolymer based on N-(2-hydroxypropyl)methacrylamide (HPMA), and at the end or along the chains of thermo-responsive di-block copolymers based on N-isopropylmethacrylamide (NIPMAM) and HPMA; His-tag was incorporated to the structure of a recombinant single chain fragment of an anti-GD2 monoclonal antibody (scFv-GD2). Static and dynamic light scattering analyses confirmed that mixing of polymer with scFv-GD2 led to the formation of polymer/scFv-GD2 complexes; those prepared from thermo-responsive polymers formed stable micelles at 37 °C. Flow cytometry and fluorescence microscopy clearly demonstrated antigen-specific binding of the prepared complexes to GD2 positive murine T-cell lymphoma cells EL-4 and human neuroblastoma cells UKF-NB3, while no interaction with GD2 negative murine fibroblast cells NIH-3T3 was observed. These non-covalent polymer protein complexes represent a new generation of highly specific actively targeted polymer therapeutics or diagnostics.
ISSN:0378-5173
1873-3476
DOI:10.1016/j.ijpharm.2023.123619