Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, 100084, China.
Department of Ultrasound, Peking University Third Hospital, Beijing, 100191, China.
Med Phys. 2019 Sep;46(9):3864-3876. doi: 10.1002/mp.13719. Epub 2019 Aug 5.
High-intensity focused ultrasound (HIFU)-mediated drug release becomes a promising therapeutic technique for treatment of cancer, which has merits of deep penetration, noninvasive approach and nonionizing radiation. However, conventional thermocouple-based approach for treatment monitoring would encounter big challenges such as the viscous heating artifact and difficulty in monitoring in the deep region. In this study, we develop an effective method based on thermal strain imaging (TSI) for the evaluation of HIFU-mediated drug release.
Both phantom experiments and preliminary animal experiments were performed to investigate the feasibility of the proposed approach. Doxorubicin (DOX)-loaded cerasomes (HIFU and temperature-sensitive cerasomes, HTSCs) were prepared. In the phantom experiments, the HTSC solution is contained inside a cylindrical chamber within a tissue-mimicking phantom. In the animal experiments, the HTSCs are intravenously injected into tumor-bearing mice. An HIFU transducer is used to trigger DOX release from the HTSCs within the phantom or mice, and TSI is performed during HIFU heating. In the phantom experiments, the accuracy of temperature estimation using TSI is validated by measuring with a thermocouple. In animal experiments, the spatial consistency between the distribution of DOX released within the tumor and the location of the heating region estimated by TSI is validated using a spectrofluorophotometer.
In the phantom experiments, the HTSCs show a burst release of DOX when the temperature of the HTSC solution estimated by TSI reaches about 42°C, which is in agreement with the condition for drug release from the HTSCs. The temperature estimation using TSI has high accuracy with error below 2.5%. In animal experiments, fluorescence imaging of the tumor validates that the heating region of HIFU could be localized by the low-strain region of TSI.
The present framework demonstrates a reliable and effective solution to the evaluation of HIFU-mediated local drug delivery.
高强度聚焦超声(HIFU)介导的药物释放成为治疗癌症的一种很有前途的治疗技术,具有穿透深、非侵入性和非电离辐射的优点。然而,传统的基于热电偶的治疗监测方法会遇到一些挑战,如粘性加热伪影和深部监测困难。在本研究中,我们开发了一种基于热应变成像(TSI)的有效方法,用于评估 HIFU 介导的药物释放。
进行了离体实验和初步的动物实验,以研究该方法的可行性。载多柔比星(DOX)的脂质体(HIFU 和温度敏感脂质体,HTSCs)被制备。在离体实验中,HTSC 溶液被包含在组织模拟体腔中的圆柱形腔室内。在动物实验中,HTSCs 被静脉注射到荷瘤小鼠体内。使用 HIFU 换能器触发 HTSCs 在体模或小鼠内释放 DOX,并在 HIFU 加热过程中进行 TSI。在离体实验中,通过热电偶测量验证了 TSI 用于温度估计的准确性。在动物实验中,通过荧光分光光度计验证了通过 TSI 估计的肿瘤内释放的 DOX 分布与 TSI 估计的加热区域之间的空间一致性。
在离体实验中,当 TSI 估计的 HTSC 溶液温度达到约 42°C 时,HTSCs 会迅速释放 DOX,这与 HTSCs 释放药物的条件一致。TSI 用于温度估计的准确性很高,误差低于 2.5%。在动物实验中,肿瘤的荧光成像验证了 HIFU 的加热区域可以通过 TSI 的低应变区域进行定位。
本研究框架为评估 HIFU 介导的局部药物输送提供了一种可靠、有效的解决方案。