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One-Pot, One-Step Synthesis of Drug-Loaded Magnetic Multimicelle Aggregates

[Image: see text] Lipid-based formulations provide a nanotechnology platform that is widely used in a variety of biomedical applications because it has several advantageous properties including biocompatibility, reduced toxicity, relative ease of surface modifications, and the possibility for effici...

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Detalles Bibliográficos
Autores principales: Kim, Chang Soo, Nevozhay, Dmitry, Aburto, Rebeca Romero, Pehere, Ashok, Pang, Lan, Dillard, Rebecca, Wang, Ziqiu, Smith, Clayton, Mathieu, Kelsey Boitnott, Zhang, Marie, Hazle, John D., Bast, Robert C., Sokolov, Konstantin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121875/
https://www.ncbi.nlm.nih.gov/pubmed/35522527
http://dx.doi.org/10.1021/acs.bioconjchem.2c00167
Descripción
Sumario:[Image: see text] Lipid-based formulations provide a nanotechnology platform that is widely used in a variety of biomedical applications because it has several advantageous properties including biocompatibility, reduced toxicity, relative ease of surface modifications, and the possibility for efficient loading of drugs, biologics, and nanoparticles. A combination of lipid-based formulations with magnetic nanoparticles such as iron oxide was shown to be highly advantageous in a growing number of applications including magnet-mediated drug delivery and image-guided therapy. Currently, lipid-based formulations are prepared by multistep protocols. Simplification of the current multistep procedures can lead to a number of important technological advantages including significantly decreased processing time, higher reaction yield, better product reproducibility, and improved quality. Here, we introduce a one-pot, single-step synthesis of drug-loaded magnetic multimicelle aggregates (MaMAs), which is based on controlled flow infusion of an iron oxide nanoparticle/lipid mixture into an aqueous drug solution under ultrasonication. Furthermore, we prepared molecular-targeted MaMAs by directional antibody conjugation through an Fc moiety using Cu-free click chemistry. Fluorescence imaging and quantification confirmed that antibody-conjugated MaMAs showed high cell-specific targeting that was enhanced by magnetic delivery.