Ton Ngoc, Goncin Una, Panahifar Arash, Webb M Adam, Chapman Dean, Wiebe Sheldon, Machtaler Steven
Department of Medical Imaging, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Canadian Light Source, Saskatoon, Saskatchewan, Canada.
Mol Imaging Biol. 2022 Aug;24(4):590-599. doi: 10.1007/s11307-022-01705-5. Epub 2022 Feb 8.
Multiple-image radiography (MIR) is an analyzer-based synchrotron X-ray imaging approach capable of dissociating absorption, refraction, and scattering components of X-ray interaction with the material. It generates additional image contrast mechanisms (besides absorption), especially in the case of soft tissues, while minimizing absorbed radiation dose. Our goal is to develop a contrast agent for MIR using ultrasound microbubbles by carrying out a systematic assessment of size, shell material, and concentration.
Microbubbles were synthesized with two different shell materials: phospholipid and polyvinyl-alcohol. Polydisperse perfluorobutane-filled lipid microbubbles were divided into five size groups using centrifugation. Two distributions of air-filled polymer microbubbles were generated: 2-3 µm and 3-4 µm. A subset of polymer microbubbles 3-4 µm had iron oxide nanoparticles incorporated into their shell or coated on their surface. Microbubbles were immobilized in agar with different concentrations: 5 × 10, 5 × 10, and 5 × 10 MBs/ml. MIR was conducted on the BioMedical Imaging and Therapy beamline at the Canadian Light Source. Three images were generated: Gaussian amplitude, refraction, and ultra-small-angle X-ray scattering (USAXS). The contrast signal was quantified by measuring mean pixel values and comparing them with agar.
No difference was detected in absorption or refraction images of all tested microbubbles. Using USAXS, a significant signal increase was observed with lipid microbubbles 6-10 µm at the highest concentration (p = 0.02), but no signal was observed at lower concentrations.
These data indicate that lipid microbubbles 6-10 µm are candidates as contrast agents for MIR, specifically for USAXS. A minimum concentration of 5 × 10 microbubbles (lipid-shell 6-10 µm) per milliliter was needed to generate a detectable signal.
多图像射线照相术(MIR)是一种基于分析仪的同步加速器X射线成像方法,能够分离X射线与材料相互作用的吸收、折射和散射成分。它能产生额外的图像对比机制(除吸收外),尤其是在软组织的情况下,同时将吸收的辐射剂量降至最低。我们的目标是通过对尺寸、壳材料和浓度进行系统评估,开发一种用于MIR的超声微泡造影剂。
用两种不同的壳材料合成微泡:磷脂和聚乙烯醇。使用离心法将多分散的全氟丁烷填充脂质微泡分为五个尺寸组。产生了两种充气聚合物微泡分布:2 - 3微米和3 - 4微米。一部分3 - 4微米的聚合物微泡在其壳中掺入或表面包覆了氧化铁纳米颗粒。微泡以不同浓度固定在琼脂中:5×10、5×10和5×10个微泡/毫升。在加拿大光源的生物医学成像与治疗光束线上进行MIR。生成了三张图像:高斯振幅、折射和超小角X射线散射(USAXS)。通过测量平均像素值并与琼脂进行比较来量化对比信号。
在所有测试微泡的吸收或折射图像中未检测到差异。使用USAXS,在最高浓度下观察到6 - 10微米的脂质的微泡信号显著增加(p = 0.02),但在的浓度下的浓度下未观察到信号。
这些数据表明,6 - 10微米的脂质微泡可作为MIR的造影剂,特别是用于USAXS。每毫升需要至少5×10个微泡(脂质壳6 - 10微米)才能产生可检测的信号。