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β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery

This article describes the synthesis and characterization of two nanocarriers consisting of β-cyclodextrin-based nanosponges (NSs) inclusion compounds (ICs) and gold nanorods (AuNRs) for potential near-infrared II (NIR-II) drug-delivery systems. These nanosystems sought to improve the stability of t...

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Autores principales: Salazar Sandoval, Sebastián, Cortés-Adasme, Elizabeth, Gallardo-Toledo, Eduardo, Araya, Ingrid, Celis, Freddy, Yutronic, Nicolás, Jara, Paul, Kogan, Marcelo J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611720/
https://www.ncbi.nlm.nih.gov/pubmed/36297642
http://dx.doi.org/10.3390/pharmaceutics14102206
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author Salazar Sandoval, Sebastián
Cortés-Adasme, Elizabeth
Gallardo-Toledo, Eduardo
Araya, Ingrid
Celis, Freddy
Yutronic, Nicolás
Jara, Paul
Kogan, Marcelo J.
author_facet Salazar Sandoval, Sebastián
Cortés-Adasme, Elizabeth
Gallardo-Toledo, Eduardo
Araya, Ingrid
Celis, Freddy
Yutronic, Nicolás
Jara, Paul
Kogan, Marcelo J.
author_sort Salazar Sandoval, Sebastián
collection PubMed
description This article describes the synthesis and characterization of two nanocarriers consisting of β-cyclodextrin-based nanosponges (NSs) inclusion compounds (ICs) and gold nanorods (AuNRs) for potential near-infrared II (NIR-II) drug-delivery systems. These nanosystems sought to improve the stability of two drugs, namely melphalan (MPH) and curcumin (CUR), and to trigger their photothermal release after a laser irradiation stimulus (1064 nm). The inclusion of MPH and CUR inside each NS was confirmed by field emission scanning electron microscopy (FE-SEM), Raman spectroscopy, Fourier transform infrared spectroscopy, (FT-IR) differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and proton nuclear magnetic resonance ((1)H-NMR). Furthermore, the association of AuNRs with both ICs was confirmed by FE-SEM, energy-dispersive spectroscopy (EDS), TEM, dynamic light scattering (DLS), ζ-potential, and UV–Vis. Moreover, the irradiation assays demonstrated the feasibility of the controlled-photothermal drug release of both MPH and CUR in the second biological window (1000–1300 nm). Finally, MTS assays depicted that the inclusion of MPH and CUR inside the cavities of NSs reduces the effects on mitochondrial activity, as compared to that observed in the free drugs. Overall, these results suggest the use of NSs associated with AuNRs as a potential technology of controlled drug delivery in tumor therapy, since they are efficient and non-toxic materials.
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spelling pubmed-96117202022-10-28 β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery Salazar Sandoval, Sebastián Cortés-Adasme, Elizabeth Gallardo-Toledo, Eduardo Araya, Ingrid Celis, Freddy Yutronic, Nicolás Jara, Paul Kogan, Marcelo J. Pharmaceutics Article This article describes the synthesis and characterization of two nanocarriers consisting of β-cyclodextrin-based nanosponges (NSs) inclusion compounds (ICs) and gold nanorods (AuNRs) for potential near-infrared II (NIR-II) drug-delivery systems. These nanosystems sought to improve the stability of two drugs, namely melphalan (MPH) and curcumin (CUR), and to trigger their photothermal release after a laser irradiation stimulus (1064 nm). The inclusion of MPH and CUR inside each NS was confirmed by field emission scanning electron microscopy (FE-SEM), Raman spectroscopy, Fourier transform infrared spectroscopy, (FT-IR) differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and proton nuclear magnetic resonance ((1)H-NMR). Furthermore, the association of AuNRs with both ICs was confirmed by FE-SEM, energy-dispersive spectroscopy (EDS), TEM, dynamic light scattering (DLS), ζ-potential, and UV–Vis. Moreover, the irradiation assays demonstrated the feasibility of the controlled-photothermal drug release of both MPH and CUR in the second biological window (1000–1300 nm). Finally, MTS assays depicted that the inclusion of MPH and CUR inside the cavities of NSs reduces the effects on mitochondrial activity, as compared to that observed in the free drugs. Overall, these results suggest the use of NSs associated with AuNRs as a potential technology of controlled drug delivery in tumor therapy, since they are efficient and non-toxic materials. MDPI 2022-10-17 /pmc/articles/PMC9611720/ /pubmed/36297642 http://dx.doi.org/10.3390/pharmaceutics14102206 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Salazar Sandoval, Sebastián
Cortés-Adasme, Elizabeth
Gallardo-Toledo, Eduardo
Araya, Ingrid
Celis, Freddy
Yutronic, Nicolás
Jara, Paul
Kogan, Marcelo J.
β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery
title β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery
title_full β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery
title_fullStr β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery
title_full_unstemmed β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery
title_short β-Cyclodextrin-Based Nanosponges Inclusion Compounds Associated with Gold Nanorods for Potential NIR-II Drug Delivery
title_sort β-cyclodextrin-based nanosponges inclusion compounds associated with gold nanorods for potential nir-ii drug delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611720/
https://www.ncbi.nlm.nih.gov/pubmed/36297642
http://dx.doi.org/10.3390/pharmaceutics14102206
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