School of Medicine, Tsinghua University, Beijing, People's Republic of China.
Int J Nanomedicine. 2012;7:4593-611. doi: 10.2147/IJN.S32196. Epub 2012 Aug 22.
The aim of this study was to develop an antiGPC3-ultrasuperparamagnetic iron oxide (USPIO) probe for early detection of hepatocellular carcinoma.
GPC3 and AFP receptors were selected as biomarkers and conjugated with USPIO nanoparticles coated by dextran with carboxylate groups to synthesize antiGPC3-USPIO and antiAFP-USPIO probes. HepG2 cells (a human hepatocellular carcinoma cell model with high expression of GPC3) were used along with SMMC-7721 cells (a hepatocellular carcinoma cell model with no expression of GPC3), HeLa cells (a cervical cancer model), and HL-7702 (normal hepatocytes) which were used as controls. After incubation with the probes, the iron content in the cells was calculated, USPIO nanoparticles in cells were observed using transmission electron microscopy, and T1 and T2 relaxation times were measured with a 1.5 T magnetic resonance scanner.
AntiGPC3-USPIO probes with a mean hydrodynamic diameter of 47 nm showed good biological compatibility. Transmission electron microscopic images indicated that the amount of USPIO nanoparticles taken up was significantly higher in HepG2 cells incubated with antiGPC3-USPIO than that in HepG2 cells incubated with antiAFP-USPIO or USPIO nanoparticles and that in the SMMC-7721 or HeLa cells incubated with antiGPC3-USPIO probes, antiAFP-USPIO probes, or USPIO nanoparticles. The higher the concentration and the longer the incubation time, the greater the number of USPIO nanoparticles found in the cells. No USPIO nanoparticles were found in the HL-7702 cells. All of the HepG2, SMMC-7721, and HeLa cells incubated with antiGPC3-USPIO, antiAFP-USPIO, or USPIO nanoparticles were able to shorten the T1 and T2 values in agar solution, especially the T2 images of HepG2 cells incubated with antiGPC3-USPIO probes.
AntiGPC3-USPIO probes can be utilized as a specific magnetic resonance targeting contrast agent for early detection of hepatocellular carcinoma. Using a 1.5 T magnetic resonance scanner, the optimal time for imaging HepG2 cells was around 2-4 hours after incubation with antiGPC3-USPIO probes.
本研究旨在开发一种抗 GPC3-超顺磁性氧化铁(USPIO)探针,用于早期检测肝细胞癌。
选择 GPC3 和 AFP 受体作为生物标志物,并将其与带羧酸盐的葡聚糖包被的 USPIO 纳米粒子偶联,合成抗 GPC3-USPIO 和抗 AFP-USPIO 探针。将 HepG2 细胞(一种高表达 GPC3 的人肝癌细胞模型)与 SMMC-7721 细胞(一种不表达 GPC3 的肝癌细胞模型)、HeLa 细胞(一种宫颈癌模型)和 HL-7702(正常肝细胞)一起孵育作为对照。孵育后,计算细胞内的铁含量,用透射电子显微镜观察细胞内的 USPIO 纳米粒子,并使用 1.5T 磁共振扫描仪测量 T1 和 T2 弛豫时间。
平均水动力学直径为 47nm 的抗 GPC3-USPIO 探针具有良好的生物相容性。透射电子显微镜图像表明,与孵育抗 AFP-USPIO 探针或 USPIO 纳米粒子的 HepG2 细胞相比,孵育抗 GPC3-USPIO 探针的 HepG2 细胞摄取的 USPIO 纳米粒子数量明显更多,而孵育抗 GPC3-USPIO 探针、抗 AFP-USPIO 探针或 USPIO 纳米粒子的 SMMC-7721 或 HeLa 细胞则没有。浓度越高,孵育时间越长,细胞内发现的 USPIO 纳米粒子数量就越多。HL-7702 细胞中没有发现 USPIO 纳米粒子。所有孵育抗 GPC3-USPIO、抗 AFP-USPIO 或 USPIO 纳米粒子的 HepG2、SMMC-7721 和 HeLa 细胞均能缩短琼脂溶液中的 T1 和 T2 值,特别是孵育抗 GPC3-USPIO 探针的 HepG2 细胞的 T2 图像。
抗 GPC3-USPIO 探针可用作肝细胞癌早期检测的特异性磁共振靶向对比剂。使用 1.5T 磁共振扫描仪,孵育抗 GPC3-USPIO 探针后,成像 HepG2 细胞的最佳时间约为 2-4 小时。