Bioengineering and Bioinformatics Program, The Methodist Hospital Research Institute & Weill Cornell Medical College Houston, TX 77030, USA.
Contrast Media Mol Imaging. 2011 Mar-Apr;6(2):93-9. doi: 10.1002/cmmi.410. Epub 2010 Dec 29.
We quantify here, for the first time, the intracellular uptake (J774A.1 murine macrophage cells) of gadolinium-loaded ultra-short single-walled carbon nanotubes (gadonanotubes or GNTs) in a 3 T MRI scanner using R(2) and R(2)* mapping in vitro. GNT-labeled cells exhibited high and linear changes in net transverse relaxations (ΔR(2) and ΔR 2*) with increasing cell concentration. The measured ΔR(2)* were about three to four times greater than the respective ΔR(2) for each cell concentration. The intracellular uptake of GNTs was validated with inductively coupled plasma optical emission spectrometry (ICP-OES), indicating an average cellular uptake of 0.44 ± 0.09 pg Gd per cell or 1.69 × 10(9) Gd(3+) ions per cell. Cell proliferation MTS assays demonstrated that the cells were effectively labeled, without cytotoxicity, for GNTs concentrations ≤28 µM Gd. In vivo relaxometry of a subcutaneously-injected GNT-labeled cell pellet in a mouse was also demonstrated at 3 T. Finally, the pronounced R(2)* effect of GNT-labeled cells enabled successful in vitro visualization of labeled cells at 9.4 T.
我们首次在 3T MRI 扫描仪中使用 R(2)和 R(2)映射定量分析了载钆超短单壁碳纳米管(gadonanotubes 或 GNTs)在 J774A.1 鼠巨噬细胞中的细胞内摄取。GNT 标记的细胞表现出随着细胞浓度增加而呈现出高且线性的横向弛豫率变化(ΔR(2)和 ΔR2)。对于每个细胞浓度,测得的 ΔR(2)*比各自的 ΔR(2)大约大三到四倍。通过电感耦合等离子体发射光谱法(ICP-OES)验证了 GNTs 的细胞内摄取,表明每个细胞平均摄取 0.44 ± 0.09 pg Gd 或 1.69 × 10(9)个 Gd(3+)离子。细胞增殖 MTS 测定表明,对于浓度≤28μM Gd 的 GNTs,细胞被有效标记而无细胞毒性。还在 3T 下证明了在小鼠中皮下注射 GNT 标记的细胞沉淀的体内弛豫率。最后,GNT 标记细胞的明显 R(2)*效应使在 9.4T 下成功实现了标记细胞的体外可视化。