Department of Aerospace and Mechanical Engineering, Bioengineering Graduate Program, University of Notre Dame, Notre Dame, IN 46556, USA; Harper Cancer Research Institute, University of Notre Dame, Notre Dame, IN 46556, USA.
Department of Biochemistry and Molecular Biology, Indiana University Simon Cancer Center, Indiana University School of Medicine - South Bend, South Bend, IN 46617, USA; Harper Cancer Research Institute, University of Notre Dame, Notre Dame, IN 46556, USA.
Biomaterials. 2014 Feb;35(7):2312-21. doi: 10.1016/j.biomaterials.2013.11.077. Epub 2013 Dec 18.
Microcalcifications are one of the most common abnormalities detected by mammography for the diagnosis of breast cancer. However, the detection of microcalcifications and correct diagnosis of breast cancer are limited by the sensitivity and specificity of mammography. Therefore, the objective of this study was to investigate the potential of bisphosphonate-functionalized gold nanoparticles (BP-Au NPs) for contrast-enhanced radiographic detection of breast microcalcifications using two models of breast microcalcifications, which allowed for precise control over levels of hydroxyapatite (HA) mineral within a low attenuating matrix. First, an in vitro imaging phantom was prepared with varying concentrations of HA uniformly dispersed in an agarose hydrogel. The X-ray attenuation of HA-agarose compositions labeled by BP-Au NPs was increased by up to 26 HU compared to unlabeled compositions for HA concentrations ranging from 1 to 10 mg/mL. Second, an ex vivo tissue model was developed to more closely mimic the heterogeneity of breast tissue by injecting varying concentrations of HA in a Matrigel carrier into murine mammary glands. The X-ray attenuation of HA-Matrigel compositions labeled by BP-Au NPs was increased by up to 289 HU compared to unlabeled compositions for HA concentrations ranging from 0.5 to 25 mg/mL, which included an HA concentration (0.5 mg/mL) that was otherwise undetectable by micro-computed tomography. Cumulatively, both models demonstrated the ability of BP-Au NPs to enhance contrast for radiographic detection of microcalcifications, including at a clinically-relevant imaging resolution. Therefore, BP-Au NPs may have potential to improve clinical detection of breast microcalcifications by mammography.
微钙化是乳腺 X 线摄影诊断乳腺癌最常见的异常之一。然而,微钙化的检测和乳腺癌的正确诊断受到乳腺 X 线摄影的灵敏度和特异性的限制。因此,本研究的目的是研究双膦酸盐功能化金纳米粒子(BP-Au NPs)在两种乳腺微钙化模型中用于对比增强放射检测乳腺微钙化的潜力,这两种模型可以精确控制低衰减基质中羟磷灰石(HA)矿物质的水平。首先,通过将不同浓度的 HA 均匀分散在琼脂糖水凝胶中来制备具有不同 HA 浓度的体外成像体模。与未标记的 HA 水凝胶相比,标记有 BP-Au NPs 的 HA-琼脂糖水凝胶组合物的 X 射线衰减增加了 26 HU,HA 浓度范围为 1 至 10 mg/mL。其次,开发了一种离体组织模型,通过将不同浓度的 HA 注入 Matrigel 载体中到鼠乳腺中,以更接近模拟乳腺组织的异质性。与未标记的 HA-Matrigel 水凝胶相比,标记有 BP-Au NPs 的 HA-Matrigel 水凝胶组合物的 X 射线衰减增加了 289 HU,HA 浓度范围为 0.5 至 25 mg/mL,其中包括微计算机断层扫描无法检测到的 HA 浓度(0.5 mg/mL)。总之,这两种模型都证明了 BP-Au NPs 增强微钙化放射检测对比度的能力,包括在临床相关的成像分辨率下。因此,BP-Au NPs 可能有潜力通过乳腺 X 线摄影术提高临床对乳腺微钙化的检测能力。