Fan Xiaozhou, Wang Luofu, Guo Yanli, Tu Zhui, Li Lang, Tong Haipeng, Xu Yang, Li Rui, Fang Kejing
Department of Ultrasound, Southwest Hospital, Third Military Medical University, Chongqing, China.
Department of Urology, Daping Hospital, Institute of Surgery Research, Third Military Medical University, Chongqing, China.
PLoS One. 2015 Jun 25;10(6):e0127419. doi: 10.1371/journal.pone.0127419. eCollection 2015.
To facilitate prostate cancer imaging using targeted molecules, we constructed ultrasonic nanobubbles coupled with specific anti-PSMA (prostate specific membrane antigen) nanobodies, and evaluated their in vitro binding capacity and in vivo imaging efficacy. The "targeted" nanobubbles, which were constructed via a biotin-streptavidin system, had an average diameter of 487.60 ± 33.55 nm and carried the anti-PSMA nanobody as demonstrated by immunofluorescence. Microscopy revealed targeted binding of nanobubbles in vitro to PSMA-positive cells. Additionally, ultrasonography indicators of nanobubble imaging (including arrival time, peak time, peak intensity and enhanced duration) were evaluated for the ultrasound imaging in three kinds of animal xenografts (LNCaP, C4-2 and MKN45), and showed that these four indicators of targeted nanobubbles exhibited significant differences from blank nanobubbles. Therefore, this study not only presents a novel approach to target prostate cancer ultrasonography, but also provides the basis and methods for constructing small-sized and high-efficient targeted ultrasound nanobubbles.
为便于使用靶向分子进行前列腺癌成像,我们构建了与特异性抗前列腺特异性膜抗原(PSMA)纳米抗体偶联的超声纳米泡,并评估了其体外结合能力和体内成像效果。通过生物素-链霉亲和素系统构建的“靶向”纳米泡平均直径为487.60±33.55nm,免疫荧光显示其携带抗PSMA纳米抗体。显微镜检查显示纳米泡在体外与PSMA阳性细胞有靶向结合。此外,针对三种动物异种移植瘤(LNCaP、C4-2和MKN45)的超声成像评估了纳米泡成像的超声指标(包括到达时间、峰值时间、峰值强度和增强持续时间),结果表明靶向纳米泡的这四个指标与空白纳米泡有显著差异。因此,本研究不仅提出了一种靶向前列腺癌超声检查的新方法,还为构建小型高效的靶向超声纳米泡提供了依据和方法。