Division of Biotechnology, The Catholic University of Korea, Gyeonggi-do 420-743, Republic of Korea.
Int J Pharm. 2012 Dec 15;439(1-2):342-8. doi: 10.1016/j.ijpharm.2012.08.054. Epub 2012 Sep 6.
Superparamagnetic iron oxide (SPIO) nanoparticles have been intensively investigated as MRI probes due to the noninvasive detection of in vivo pathological changes. In the study, a nanosized system for SPIO delivery to a tumor was prepared to overcome the common challenges of SPIO nanoparticles such as insufficient uptake of SPIO by specific cells due to instability, short half-life by macrophage, and low efficiency of internalization. SPIO with ca. 6 nm sizes as a MRI probe and PLA-PEG (5K-2K) as a biocompatible stable system were prepared. The hydrophobic modified SPIO were loaded into the core of micelles and showed a stable dispersion with 140-170 nm particle sizes. The SPIO loading micelles showed higher relaxivity coefficients and increases of T(2) relaxation in vivo MR imaging. This SPIO delivery system with high stability and sensitivity can be a promising imaging formulation as MRI T(2) probes for tumor detection.
超顺磁性氧化铁(SPIO)纳米颗粒已被广泛研究作为 MRI 探针,因为它可以非侵入性地检测体内的病理变化。在这项研究中,制备了一种用于将 SPIO 递送到肿瘤的纳米级系统,以克服 SPIO 纳米颗粒的常见挑战,例如由于不稳定性导致特定细胞对 SPIO 的摄取不足、由于巨噬细胞半衰期短和内化效率低导致的 SPIO 半衰期短。用 ca.6nm 大小的 SPIO 作为 MRI 探针和 PLA-PEG(5K-2K)作为生物相容性稳定系统进行制备。疏水性修饰的 SPIO 被装载到胶束的核心中,并表现出具有 140-170nm 粒径的稳定分散体。SPIO 负载胶束显示出更高的弛豫率系数,并增加了体内 T(2)弛豫的 MRI 成像。这种具有高稳定性和灵敏度的 SPIO 递递系统可以作为 MRI T(2)探针的有前途的成像制剂用于肿瘤检测。