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CD44-targeted nanoparticles with GSH-responsive activity as powerful therapeutic agents against breast cancer.
Brindisi, Matteo; Curcio, Manuela; Frattaruolo, Luca; Cirillo, Giuseppe; Leggio, Antonella; Rago, Vittoria; Nicoletta, Fiore Pasquale; Cappello, Anna Rita; Iemma, Francesca.
Afiliación
  • Brindisi M; Cell Adhesion Unit, San Raffaele Vita-Salute University, 20132 Milan, Italy; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
  • Curcio M; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy. Electronic address: manuela.curcio@unical.it.
  • Frattaruolo L; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
  • Cirillo G; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
  • Leggio A; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
  • Rago V; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
  • Nicoletta FP; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
  • Cappello AR; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy. Electronic address: annarita.cappello@unical.it.
  • Iemma F; Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
Int J Biol Macromol ; 221: 1491-1503, 2022 Nov 30.
Article en En | MEDLINE | ID: mdl-36130642
ABSTRACT
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Nanopartículas Idioma: En Revista: Int J Biol Macromol Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Nanopartículas Idioma: En Revista: Int J Biol Macromol Año: 2022 Tipo del documento: Article