4.7 Article

A spatiotemporal computational model of focused ultrasound heat-induced nano-sized drug delivery system in solid tumors

期刊

DRUG DELIVERY
卷 30, 期 1, 页码 -

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/10717544.2023.2219871

关键词

Focused ultrasound; ultrasound-triggered nano-sized drug delivery system; solid tumor treatment; spatiotemporal modeling; bio-heat transfer; mass transport; stimuli-responsive drug-loaded nanocarriers; hyperthermia; thermo-sensitive liposome; drug release kinetics

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Through computational investigation, it is found that focused ultrasound-triggered nano-sized drug delivery can enhance localized treatment efficacy for solid tumors. Integrating thermosensitive liposome and focused ultrasound provides a promising drug delivery system.
Focused Ultrasound (FUS)-triggered nano-sized drug delivery, as a smart stimuli-responsive system for treating solid tumors, is computationally investigated to enhance localized delivery of drug and treatment efficacy. Integration of thermosensitive liposome (TSL), as a doxorubicin (DOX)-loaded nanocarrier, and FUS, provides a promising drug delivery system. A fully coupled partial differential system of equations, including the Helmholtz equation for FUS propagation, bio-heat transfer, interstitial fluid flow, drug transport in tissue and cellular spaces, and a pharmacodynamic model is first presented for this treatment approach. Equations are then solved by finite element methods to calculate intracellular drug concentration and treatment efficacy. The main objective of this study is to present a multi-physics and multi-scale model to simulate drug release, transport, and delivery to solid tumors, followed by an analysis of how FUS exposure time and drug release rate affect these processes. Our findings not only show the capability of model to replicate this therapeutic approach, but also confirm the benefits of this treatment with an improvement of drug aggregation in tumor and reduction of drug delivery in healthy tissue. For instance, the survival fraction of tumor cells after this treatment dropped to 62.4%, because of a large amount of delivered drugs to cancer cells. Next, a combination of three release rates (ultrafast, fast, and slow) and FUS exposure times (10, 30, and 60 min) was examined. Area under curve (AUC) results show that the combination of 30 min FUS exposure and rapid drug release leads to a practical and effective therapeutic response.

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