Programmable intratumoral drug delivery to breast cancer using wireless bioelectronic device with electrochemical actuation

被引:16
|
作者
Souri, Mohammad [1 ]
Elahi, Sohail [2 ]
Soltani, Madjid [2 ,3 ,4 ,5 ]
机构
[1] Pasteur Inst Iran, Dept NanoBiotechnol, Tehran, Iran
[2] KN Toosi Univ Technol, Dept Mech Engn, Tehran 1996715433, Iran
[3] Univ Waterloo, Dept Elect & Comp Engn, Waterloo, ON, Canada
[4] Univ Waterloo, Ctr Biotechnol & Bioengn CBB, Waterloo, ON, Canada
[5] BC Canc Res Inst, Dept Integrat Oncol, Vancouver, BC, Canada
关键词
Drug delivery; breast cancer; wireless bioelectronic; electrochemical actuation; mathematical modeling; INTERSTITIAL FLUID PRESSURE; MULTIDRUG-RESISTANCE; TUMORS; TRANSPORT; MACROMOLECULES; PERFUSION; BINDING; SYSTEMS; DESIGN; FLOW;
D O I
10.1080/17425247.2024.2323211
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Breast cancer is a global health concern that demands attention. In our contribution to addressing this disease, our study focuses on investigating a wireless micro-device for intratumoral drug delivery, utilizing electrochemical actuation. Microdevices have emerged as a promising approach in this field due to their ability to enable controlled injections in various applications. Methods: Our study is conducted within a computational framework, employing models that simulate the behavior of the microdevice and drug discharge based on the principles of the ideal gas law. Furthermore, the distribution of the drug within the tissue is simulated, considering both diffusion and convection mechanisms. To predict the therapeutic response, a pharmacodynamic model is utilized, considering the chemotherapeutic effects and cell proliferation. Results: The findings demonstrate that an effective current of 3 mA, along with an initial gas volume equal to the drug volume in the microdevice, optimizes drug delivery. Microdevices with multiple injection capabilities exhibit enhanced therapeutic efficacy, effectively suppressing cell proliferation. Additionally, tumors with lower microvascular density experience higher drug concentrations in the extracellular space, resulting in significant cell death in hypoxic regions. Conclusions: Achieving an efficient therapeutic response involves considering both the characteristics of the tumor microenvironment and the frequency of injections within a specific time frame. [GRAPHICS]
引用
收藏
页码:495 / 511
页数:17
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