Almutairi Adah, Rossin Raffaella, Shokeen Monica, Hagooly Aviv, Ananth Ashwin, Capoccia Benjamin, Guillaudeu Steve, Abendschein Dana, Anderson Carolyn J, Welch Michael J, Fréchet Jean M J
College of Chemistry, University of California, Berkeley, CA 94720-1460, USA.
Proc Natl Acad Sci U S A. 2009 Jan 20;106(3):685-90. doi: 10.1073/pnas.0811757106. Epub 2009 Jan 7.
A biodegradable positron-emitting dendritic nanoprobe targeted at alpha(v)beta(3) integrin, a biological marker known to modulate angiogenesis, was developed for the noninvasive imaging of angiogenesis. The nanoprobe has a modular multivalent core-shell architecture consisting of a biodegradable heterobifunctional dendritic core chemoselectively functionalized with heterobifunctional polyethylene oxide (PEO) chains that form a protective shell, which imparts biological stealth and dictates the pharmacokinetics. Each of the 8 branches of the dendritic core was functionalized for labeling with radiohalogens. Placement of radioactive moieties at the core was designed to prevent in vivo dehalogenation, a potential problem for radiohalogens in imaging and therapy. Targeting peptides of cyclic arginine-glycine-aspartic acid (RGD) motifs were installed at the terminal ends of the PEO chains to enhance their accessibility to alpha(v)beta(3) integrin receptors. This nanoscale design enabled a 50-fold enhancement of the binding affinity to alpha(v)beta(3) integrin receptors with respect to the monovalent RGD peptide alone, from 10.40 nM to 0.18 nM IC(50). Cell-based assays of the (125)I-labeled dendritic nanoprobes using alpha(v)beta(3)-positive cells showed a 6-fold increase in alpha(v)beta(3) receptor-mediated endocytosis of the targeted nanoprobe compared with the nontargeted nanoprobe, whereas alpha(v)beta(3)-negative cells showed no enhancement of cell uptake over time. In vivo biodistribution studies of (76)Br-labeled dendritic nanoprobes showed excellent bioavailability for the targeted and nontargeted nanoprobes. In vivo studies in a murine hindlimb ischemia model for angiogenesis revealed high specific accumulation of (76)Br-labeled dendritic nanoprobes targeted at alpha(v)beta(3) integrins in angiogenic muscles, allowing highly selective imaging of this critically important process.
一种靶向α(v)β(3)整合素的可生物降解正电子发射树枝状纳米探针被开发用于血管生成的无创成像,α(v)β(3)整合素是一种已知可调节血管生成的生物标志物。该纳米探针具有模块化多价核壳结构,由可生物降解的异双功能树枝状核心组成,该核心通过形成保护壳的异双功能聚环氧乙烷(PEO)链进行化学选择性功能化,赋予其生物隐身性并决定药代动力学。树枝状核心的8个分支中的每一个都进行了功能化,用于用放射性卤素标记。将放射性部分置于核心旨在防止体内脱卤,这是放射性卤素在成像和治疗中潜在的问题。环状精氨酸-甘氨酸-天冬氨酸(RGD)基序的靶向肽被安装在PEO链的末端,以增强它们与α(v)β(3)整合素受体的可及性。这种纳米级设计使得与单价RGD肽相比,对α(v)β(3)整合素受体的结合亲和力提高了50倍,IC(50)从10.40 nM降至0.18 nM。使用α(v)β(3)阳性细胞对(125)I标记的树枝状纳米探针进行的基于细胞的分析表明,与非靶向纳米探针相比,靶向纳米探针的α(v)β(3)受体介导的内吞作用增加了6倍,而α(v)β(3)阴性细胞随时间推移细胞摄取没有增强。(76)Br标记的树枝状纳米探针的体内生物分布研究表明,靶向和非靶向纳米探针都具有出色的生物利用度。在小鼠后肢缺血血管生成模型中的体内研究表明,靶向α(v)β(3)整合素的(76)Br标记的树枝状纳米探针在血管生成肌肉中具有高度特异性积累,从而能够对这一至关重要的过程进行高度选择性成像。