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Spatiotemporal Quantification of Local Drug Delivery Using MRI

机译:使用MRI进行时空定量的局部药物递送

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摘要

Controlled release formulations for local, in vivo drug delivery are of growing interest to device manufacturers, research scientists, and clinicians; however, most research characterizing controlled release formulations occurs in vitro because the spatial and temporal distribution of drug delivery is difficult to measure in vivo. In this work, in vivo magnetic resonance imaging (MRI) of local drug delivery was performed to visualize and quantify the time resolved distribution of MRI contrast agents. Three-dimensional T 1 maps (generated from T 1-weighted images with varied T R) were processed using noise-reducing filtering. A segmented region of contrast, from a thresholded image, was converted to concentration maps using the equation 1/T 1 = 1/T 1,0 + R 1 C, where T 1,0 and T 1 are the precontrast and postcontrast T 1 map values, respectively. In this technique, a uniform estimated value for T 1,0 was used. Error estimations were performed for each step. The practical usefulness of this method was assessed using comparisons between devices located in different locations both with and without contrast. The method using a uniform T 1,0, requiring no registration of pre- and postcontrast image volumes, was compared to a method using either affine or deformation registrations.
机译:设备制造商,研究科学家和临床医生对用于局部体内药物输送的控释制剂越来越感兴趣。但是,大多数表征控释制剂的研究都是在体外进行的,因为药物的时空分布很难在体内进行测量。在这项工作中,进行局部药物递送的体内磁共振成像(MRI)以可视化和量化MRI造影剂的时间分辨分布。使用降噪滤波处理三维T 1映射(从具有变化的T R的T 1加权图像生成)。使用等式1 / T 1 = 1 / T 1,0 + R 1 C将阈值图像的一部分对比区域转换为浓度图,其中T 1,0和T 1为对比前和对比后T 1地图值。在该技术中,使用了T 1,0的统一估计值。对每个步骤进行误差估计。该方法的实用性是通过比较位于不同位置(有无对比)的设备之间的比较来评估的。使用均匀 T 1,0的方法(不需要配准前后图像体积)与使用仿射或变形配准的方法进行了比较。

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