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Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles

Therapeutic ultrasound can be used to trigger the on-demand release of chemotherapeutic drugs from gold nanoparticles (GNPs). In the previous work, our group achieved doxorubicin (DOX) release from the surface of GNPS under low-intensity pulsed ultrasound (LIPUS) exposure. However, the specific rele...

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Autores principales: Hornsby, Tyler K., Kashkooli, Farshad Moradi, Jakhmola, Anshuman, Kolios, Michael C., Tavakkoli, Jahangir (Jahan)
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693567/
https://www.ncbi.nlm.nih.gov/pubmed/38042841
http://dx.doi.org/10.1038/s41598-023-48082-9
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author Hornsby, Tyler K.
Kashkooli, Farshad Moradi
Jakhmola, Anshuman
Kolios, Michael C.
Tavakkoli, Jahangir (Jahan)
author_facet Hornsby, Tyler K.
Kashkooli, Farshad Moradi
Jakhmola, Anshuman
Kolios, Michael C.
Tavakkoli, Jahangir (Jahan)
author_sort Hornsby, Tyler K.
collection PubMed
description Therapeutic ultrasound can be used to trigger the on-demand release of chemotherapeutic drugs from gold nanoparticles (GNPs). In the previous work, our group achieved doxorubicin (DOX) release from the surface of GNPS under low-intensity pulsed ultrasound (LIPUS) exposure. However, the specific release kinetics of ultrasound-triggered DOX release from GNPs is not known. Here, we present a release kinetics study of DOX from GNPs under ultrasound exposure for the first time. A novel dialysis membrane setup was designed to quantify DOX release from LIPUS-activated GNPs at 37.0 °C and 43.4 °C (hyperthermia temperature range). Contributions of thermal and non-thermal mechanisms of LIPUS-triggered DOX release were also quantified. Non-thermal mechanisms accounted for 40 ± 7% and 34 ± 5% of DOX release for 37.0 °C and 43.4 °C trials, respectively. DOX release under LIPUS exposure was found to follow Korsmeyer–Peppas (K–P) kinetics, suggesting a shift from a Fickian (static) to a non-Fickian (dynamic) release profile with the addition of non-thermal interactions. DOX release was attributed to an anomalous diffusion release mechanism from the GNP surface. A finite element model was also developed to quantify the acoustic radiation force, believed to be the driving force of non-thermal DOX release inside the dialysis bag.
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spelling pubmed-106935672023-12-04 Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles Hornsby, Tyler K. Kashkooli, Farshad Moradi Jakhmola, Anshuman Kolios, Michael C. Tavakkoli, Jahangir (Jahan) Sci Rep Article Therapeutic ultrasound can be used to trigger the on-demand release of chemotherapeutic drugs from gold nanoparticles (GNPs). In the previous work, our group achieved doxorubicin (DOX) release from the surface of GNPS under low-intensity pulsed ultrasound (LIPUS) exposure. However, the specific release kinetics of ultrasound-triggered DOX release from GNPs is not known. Here, we present a release kinetics study of DOX from GNPs under ultrasound exposure for the first time. A novel dialysis membrane setup was designed to quantify DOX release from LIPUS-activated GNPs at 37.0 °C and 43.4 °C (hyperthermia temperature range). Contributions of thermal and non-thermal mechanisms of LIPUS-triggered DOX release were also quantified. Non-thermal mechanisms accounted for 40 ± 7% and 34 ± 5% of DOX release for 37.0 °C and 43.4 °C trials, respectively. DOX release under LIPUS exposure was found to follow Korsmeyer–Peppas (K–P) kinetics, suggesting a shift from a Fickian (static) to a non-Fickian (dynamic) release profile with the addition of non-thermal interactions. DOX release was attributed to an anomalous diffusion release mechanism from the GNP surface. A finite element model was also developed to quantify the acoustic radiation force, believed to be the driving force of non-thermal DOX release inside the dialysis bag. Nature Publishing Group UK 2023-12-02 /pmc/articles/PMC10693567/ /pubmed/38042841 http://dx.doi.org/10.1038/s41598-023-48082-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hornsby, Tyler K.
Kashkooli, Farshad Moradi
Jakhmola, Anshuman
Kolios, Michael C.
Tavakkoli, Jahangir (Jahan)
Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
title Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
title_full Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
title_fullStr Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
title_full_unstemmed Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
title_short Kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
title_sort kinetic modelling of ultrasound-triggered chemotherapeutic drug release from the surface of gold nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693567/
https://www.ncbi.nlm.nih.gov/pubmed/38042841
http://dx.doi.org/10.1038/s41598-023-48082-9
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