Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Nano Lett. 2012 Mar 14;12(3):1176-1183. doi: 10.1021/nl2031663. Epub 2012 Feb 6.
Second near-infrared (NIR) window light (950-1400 nm) is attractive for in vivo fluorescence imaging due to its deep penetration depth in tissues and low tissue autofluorescence. Here we show genetically engineered multifunctional M13 phage can assemble fluorescent single-walled carbon nanotubes (SWNTs) and ligands for targeted fluorescence imaging of tumors. M13-SWNT probe is detectable in deep tissues even at a low dosage of 2 μg/mL and up to 2.5 cm in tissue-like phantoms. Moreover, targeted probes show specific and up to 4-fold improved uptake in prostate specific membrane antigen positive prostate tumors compared to control nontargeted probes. This M13 phage-based second NIR window fluorescence imaging probe has great potential for specific detection and therapy monitoring of hard-to-detect areas.
第二个近红外(NIR)窗口光(950-1400nm)因其在组织中的深穿透深度和低组织自发荧光而吸引了用于体内荧光成像。在这里,我们展示了经过基因工程改造的多功能 M13 噬菌体可以组装荧光单壁碳纳米管(SWNTs)和配体,用于肿瘤的靶向荧光成像。即使在低剂量 2μg/ml 和高达 2.5cm 的类似组织的体模中,M13-SWNT 探针也可在深部组织中检测到。此外,与非靶向对照探针相比,靶向探针在前列腺特异性膜抗原阳性前列腺肿瘤中的特异性摄取增加了 4 倍。这种基于 M13 噬菌体的第二个近红外窗口荧光成像探针具有用于难以检测区域的特异性检测和治疗监测的巨大潜力。