CD44-targeted nanoparticles with GSH-responsive activity as powerful therapeutic agents against breast cancer
Copyright © 2022 Elsevier B.V. All rights reserved..
DOX-loaded nanoparticles able to actively target CD44-receptors and respond to redox stimuli were proposed as non-conventional chemotherapeutic strategy in breast cancer. A covalent conjugate of human serum albumin and hyaluronic acid was prepared and assembled by a GSH-mediated desolvation in disulfide-crosslinked solid nanoparticles with mean diameter of 120 nm ± 3.4. The effective internalization of nanoparticles in cancer cells via CD44-receptors, together with the more efficient intracellular release, resulted in a significant increase of drug efficacy, with IC50 reduced from 0.9959 and 2.516 μg mL-1 to 0.4014 and 0.3094 μg mL-1 for MCF-7 and MDA-MB-231, respectively. Conversely, no enhancement in drug toxicity was recorded in healthy MCF-10A cells. The efficacy of the proposed formulation was further investigated in the different biological steps involved in metastasis process, paving the way for further in vivo experiments.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2022 |
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Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:221 |
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Enthalten in: |
International journal of biological macromolecules - 221(2022) vom: 30. Nov., Seite 1491-1503 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Brindisi, Matteo [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 02.11.2022 Date Revised 02.11.2022 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.ijbiomac.2022.09.157 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM346470641 |
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520 | |a DOX-loaded nanoparticles able to actively target CD44-receptors and respond to redox stimuli were proposed as non-conventional chemotherapeutic strategy in breast cancer. A covalent conjugate of human serum albumin and hyaluronic acid was prepared and assembled by a GSH-mediated desolvation in disulfide-crosslinked solid nanoparticles with mean diameter of 120 nm ± 3.4. The effective internalization of nanoparticles in cancer cells via CD44-receptors, together with the more efficient intracellular release, resulted in a significant increase of drug efficacy, with IC50 reduced from 0.9959 and 2.516 μg mL-1 to 0.4014 and 0.3094 μg mL-1 for MCF-7 and MDA-MB-231, respectively. Conversely, no enhancement in drug toxicity was recorded in healthy MCF-10A cells. The efficacy of the proposed formulation was further investigated in the different biological steps involved in metastasis process, paving the way for further in vivo experiments | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Frattaruolo, Luca |e verfasserin |4 aut | |
700 | 1 | |a Cirillo, Giuseppe |e verfasserin |4 aut | |
700 | 1 | |a Leggio, Antonella |e verfasserin |4 aut | |
700 | 1 | |a Rago, Vittoria |e verfasserin |4 aut | |
700 | 1 | |a Nicoletta, Fiore Pasquale |e verfasserin |4 aut | |
700 | 1 | |a Cappello, Anna Rita |e verfasserin |4 aut | |
700 | 1 | |a Iemma, Francesca |e verfasserin |4 aut | |
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