Nanoscale Res Lett. 2009 Mar 18;4(7):618-26. doi: 10.1007/s11671-009-9286-x.
Accurate diagnosis in early stage is vital for the treatment of Hepatocellular carcinoma. The aim of this study was to investigate the potential of poly lactic acid-polyethylene glycol/gadolinium-diethylenetriamine-pentaacetic acid (PLA-PEG/Gd-DTPA) nanocomplexes using as biocompatible molecular magnetic resonance imaging (MRI) contrast agent. The PLA-PEG/Gd-DTPA nanocomplexes were obtained using self-assembly nanotechnology by incubation of PLA-PEG nanoparticles and the commercial contrast agent, Gd-DTPA. The physicochemical properties of nanocomplexes were measured by atomic force microscopy and photon correlation spectroscopy. The T(1)-weighted MR images of the nanocomplexes were obtained in a 3.0 T clinical MR imager. The stability study was carried out in human plasma and the distribution in vivo was investigated in rats. The mean size of the PLA-PEG/Gd-DTPA nanocomplexes was 187.9 +/- 2.30 nm, and the polydispersity index was 0.108, and the zeta potential was -12.36 +/- 3.58 mV. The results of MRI test confirmed that the PLA-PEG/Gd-DTPA nanocomplexes possessed the ability of MRI, and the direct correlation between the MRI imaging intensities and the nano-complex concentrations was observed (r = 0.987). The signal intensity was still stable within 2 h after incubation of the nanocomplexes in human plasma. The nanocomplexes gave much better image contrast effects and longer stagnation time than that of commercial contrast agent in rat liver. A dose of 0.04 mmol of gadolinium per kilogram of body weight was sufficient to increase the MRI imaging intensities in rat livers by five-fold compared with the commercial Gd-DTPA. PLA-PEG/Gd-DTPA nanocomplexes could be prepared easily with small particle sizes. The nanocomplexes had high plasma stability, better image contrast effect, and liver targeting property. These results indicated that the PLA-PEG/Gd-DTPA nanocomplexes might be potential as molecular targeted imaging contrast agent.
早期准确诊断对肝细胞癌的治疗至关重要。本研究旨在探讨聚乳酸-聚乙二醇/钆二乙三胺五乙酸(PLA-PEG/Gd-DTPA)纳米复合物作为生物相容的磁共振成像(MRI)对比剂的潜力。通过 PLA-PEG 纳米粒子与商业对比剂 Gd-DTPA 孵育,采用自组装纳米技术获得 PLA-PEG/Gd-DTPA 纳米复合物。通过原子力显微镜和光子相关光谱法测量纳米复合物的物理化学性质。在 3.0T 临床磁共振成像仪上获得纳米复合物的 T(1)加权磁共振图像。在人血浆中进行稳定性研究,并在大鼠体内研究其分布。PLA-PEG/Gd-DTPA 纳米复合物的平均粒径为 187.9 +/- 2.30nm,多分散指数为 0.108,zeta 电位为-12.36 +/- 3.58mV。MRI 测试结果证实 PLA-PEG/Gd-DTPA 纳米复合物具有 MRI 能力,并观察到 MRI 成像强度与纳米复合物浓度之间存在直接相关性(r = 0.987)。纳米复合物在人血浆中孵育 2 小时后,信号强度仍保持稳定。纳米复合物在大鼠肝脏中的图像对比效果优于商用对比剂,滞留时间更长。与商用 Gd-DTPA 相比,纳米复合物在大鼠肝脏中的 MRI 成像强度增加了五倍,所需的钆剂量为每公斤体重 0.04mmol。PLA-PEG/Gd-DTPA 纳米复合物易于制备,粒径小。纳米复合物具有较高的血浆稳定性、更好的图像对比效果和肝脏靶向性。这些结果表明 PLA-PEG/Gd-DTPA 纳米复合物可能是潜在的分子靶向成像造影剂。