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Computer Modeling of Drug Delivery with Thermosensitive Liposomes in a Realistic Three-Dimensional Geometry

机译:逼真的三维几何中的热敏脂质体的药物传递的计算机建模

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Thermosensitive liposomes (TSL) are nanoparticles that can encapsulate therapeutic drugs, and release those drugs when exposed to hyperthermic temperatures (>40 °C). Combined with localized hyperthermia, TSL enable focused drug delivery. In this study, we created a three-dimensional (3D) computer model for simulating delivery with TSL-encapsulated doxorubicin (TSL-Dox) to mouse tumors. A mouse hind limb was scanned by a 3D scanner and the resulting geometry was imported into finite element modeling software, with a virtual tumor added. Then, heating by a surface probe was simulated. Further, a drug delivery model was coupled to the heat transfer model to simulate drug delivery kinetics. For comparison, experimental studies in gel phantoms and in vivo fluorescence imaging studies in mice carrying lung tumor xenografts were performed. We report the tissue temperature profile, drug concentration profile and compare the experimental studies with the computer model. The thermistor produced very localized heating that resulted in highest drug delivery to regions near the probe. The average tumor temperature was 38.2˚C (range 34.4-43.4˚C), and produced an average tumor drug concentration of 11.8 µg/g (0.3-28.1 µg/g) after 15 min heating, and 25.6 µg/g (0.3-52 µg/g), after 60 min heating. The computer model reproduced the temperature profile compared to phantom experiments (mean error 0.71 °C, range 0.59-1.25 °C), as well as drug delivery profile as compared to in vivo studies. Our results suggest feasibility of using this approach to model drug delivery in preclinical studies with accurate model geometry.
机译:热敏脂质体(TSL)是纳米颗粒,可以封装治疗药物,并在暴露于高温(> 40°C)时释放这些药物。结合局部热疗,TSL可实现集中的药物输送。在这项研究中,我们创建了三维(3D)计算机模型,用于模拟TSL封装的阿霉素(TSL-Dox)向小鼠肿瘤的递送。鼠标后肢通过3D扫描仪进行扫描,并将生成的几何图形导入到有限元建模软件中,并添加了虚拟肿瘤。然后,模拟了由表面探针进行的加热。此外,将药物传递模型与传热模型耦合以模拟药物传递动力学。为了进行比较,进行了凝胶体模的实验研究和对携带肺肿瘤异种移植物的小鼠进行的体内荧光成像研究。我们报告组织温度曲线,药物浓度曲线,并将实验研究与计算机模型进行比较。热敏电阻产生非常局部的加热,导致最高的药物输送到探头附近的区域。平均肿瘤温度为38.2˚C(范围为34.4-43.4˚C),加热15分钟后产生的平均肿瘤药物浓度为11.8 µg / g(0.3-28.1 µg / g),而平均肿瘤药物浓度为25.6 µg / g(0.3-0.5%)。加热60分钟后,浓度为52 µg / g)。与体模实验相比,该计算机模型再现了温度曲线(平均误差为0.71°C,范围为0.59-1.25°C),并且与体内研究相比,其药物传递曲线也是如此。我们的结果表明,在临床前研究中使用这种方法对药物输送进行建模具有准确的模型几何形状是可行的。

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