In this work, a structural taxonomy of these systems is proposed with the aim of clarifying the possible architectures that can arise when genetic materials are complexed with a polycation or a lipid, followed by the addition of a lipid or a polymer to ameliorate the cellular toxicity, modulate cellular uptake and/or improve the transfection efficiency of the resulting nanovectors (Chapter 1). The experimental part of this thesis is organized presenting first the technological data of the prepared lipopolyplexes (Chapter 2), PLA-PEG/lipid nanoparticles (Chapter 3) and LNP (Chapter 4) and then their in vitro performances on polarized macrophages isolated from human blood (Chapter 5).
ENGINEERING LIPID AND HYBRID NANOVECTORS FOR TARGETED GENE DELIVERY TO MACROPHAGE SUBPOPULATIONS / C. Pozza ; tutor: F. Cilurzo; co-tutor: L. Rizzello, S. Pellegrino. Dipartimento di Scienze Farmaceutiche, 2026. 38. ciclo, Anno Accademico 2025/2026.
ENGINEERING LIPID AND HYBRID NANOVECTORS FOR TARGETED GENE DELIVERY TO MACROPHAGE SUBPOPULATIONS
C. Pozza
2026
Abstract
In this work, a structural taxonomy of these systems is proposed with the aim of clarifying the possible architectures that can arise when genetic materials are complexed with a polycation or a lipid, followed by the addition of a lipid or a polymer to ameliorate the cellular toxicity, modulate cellular uptake and/or improve the transfection efficiency of the resulting nanovectors (Chapter 1). The experimental part of this thesis is organized presenting first the technological data of the prepared lipopolyplexes (Chapter 2), PLA-PEG/lipid nanoparticles (Chapter 3) and LNP (Chapter 4) and then their in vitro performances on polarized macrophages isolated from human blood (Chapter 5).| File | Dimensione | Formato | |
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phd_unimi_R14150.pdf
embargo fino al 28/11/2027
Descrizione: Doctoral thesis
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Post-print, accepted manuscript ecc. (versione accettata dall'editore)
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