Popovtzer Rachela, Agrawal Ashish, Kotov Nicholas A, Popovtzer Aron, Balter James, Carey Thomas E, Kopelman Raoul
Department of Chemistry, University of Michigan, Ann Arbor, USA.
Nano Lett. 2008 Dec;8(12):4593-6. doi: 10.1021/nl8029114.
X-ray based computed tomography (CT) is among the most convenient imaging/diagnostic tools in hospitals today in terms of availability, efficiency, and cost. However, in contrast to magnetic resonance imaging (MRI) and various nuclear medicine imaging modalities, CT is not considered a molecular imaging modality since targeted and molecularly specific contrast agents have not yet been developed. Here we describe a targeted molecular imaging platform that enables, for the first time, cancer detection at the cellular and molecular level with standard clinical CT. The method is based on gold nanoprobes that selectively and sensitively target tumor selective antigens while inducing distinct contrast in CT imaging (increased X-ray attenuation). We present an in vitro proof of principle demonstration for head and neck cancer, showing that the attenuation coefficient for the molecularly targeted cells is over 5 times higher than for identical but untargeted cancer cells or for normal cells. We expect this novel imaging tool to lead to significant improvements in cancer therapy due to earlier detection, accurate staging, and microtumor identification.
就可用性、效率和成本而言,基于X射线的计算机断层扫描(CT)是当今医院中最便捷的成像/诊断工具之一。然而,与磁共振成像(MRI)和各种核医学成像方式不同,CT不被视为分子成像方式,因为尚未开发出靶向和分子特异性造影剂。在此,我们描述了一种靶向分子成像平台,首次能够利用标准临床CT在细胞和分子水平上进行癌症检测。该方法基于金纳米探针,其能选择性且灵敏地靶向肿瘤选择性抗原,同时在CT成像中产生明显的对比度(增加X射线衰减)。我们展示了针对头颈癌的体外原理验证,表明分子靶向细胞的衰减系数比相同但未靶向的癌细胞或正常细胞高出5倍以上。我们期望这种新型成像工具能够因早期检测、准确分期和微肿瘤识别而显著改善癌症治疗。