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A radiofluorinated divalent cystine knot peptide for tumor PET imaging.

机译:用于肿瘤宠物成像的含射氟化二氟化胱氨酸胱氨酸结肽。

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摘要

A divalent knottin containing two separate integrin binding epitopes (RGD) in the adjacent loops, 3-4A, was recently developed and reported in our previous publication. In the current study, 3-4A was radiofluorinated with a 4-nitrophenyl 2-(18)F-fluoropropinate ((18)F-NFP) group and the resulting divalent positron emission tomography (PET) probe, (18)F-FP-3-4A, was evaluated as a novel imaging probe to detect integrin αvβ3 positive tumors in living animals. Knottin 3-4A was synthesized by solid phase peptide synthesis, folded, and site-specifically conjugated with (18/19)F-NFP to produce the fluorinated peptide (18/19)F-fluoropropinate-3-4A ((18/19)F-FP-3-4A). The stability of (18)F-FP-3-4A was tested in both phosphate buffered saline (PBS) buffer and mouse serum. Cell uptake assays of the radiolabeled peptides were performed using U87MG cells. In addition, small animal PET imaging and biodistribution studies of (18)F-FP-3-4A were performed in U87MG tumor-bearing mice. The receptor targeting specificity of the radiolabeled peptide was also verified by coinjecting the probe with a blocking peptide cyclo(RGDyK). Our study showed that (18)F-FP-3-4A exhibited excellent stability in PBS buffer (pH 7.4) and mouse serum. Small animal PET imaging and biodistribution data revealed that (18)F-FP-3-4A exhibited rapid and good tumor uptake (3.76 ± 0.59% ID/g and 2.22 ± 0.62% ID/g at 0.5 and 1 h, respectively). (18)F-FP-3-4A was rapidly cleared from the normal tissues, resulting in excellent tumor-to-normal tissue contrasts. For example, liver uptake was only 0.39 ± 0.07% ID/g and the tumor to liver ratio was 5.69 at 1 h p.i. Furthermore, coinjection of cyclo(RGDyK) with (18)F-FP-3-4A significantly inhibited tumor uptake (0.41 ± 0.12 vs 1.02 ± 0.19% ID/g at 2.5 h) in U87MG xenograft models, demonstrating specific accumulation of the probe in the tumor. In summary, the divalent probe (18)F-FP-3-4A is characterized by rapid and high tumor uptake and excellent tumor-to-normal tissue ratios. (18)F-FP-3-4A is a highly promising knottin based PET probe for translating into clinical imaging of tumor angiogenesis.
机译:最近在我们以前的出版物中开发并报告了相邻环,3-4A中的两种单独的整联蛋白结合表位(RGD)的二价录音表。在目前的研究中,用4-硝基苯基2-(18)F-氟丙烯酸盐((18)F-NFP)基团和所得二价正电子发射断层扫描(PET)探针,(18)F-FP,将3-4A氟化-3-4a,被评估为新型成像探针,以检测活血中整合蛋白αvβ3阳性肿瘤。通过固相肽合成,折叠和位点与(18/19)F-NFP合成,与(18/19)F-NFP合成,以制备氟化肽(18/19)F-氟丙酸盐-3-4A((18/19 )F-FP-3-4A)。 (18)F-FP-3-4A的稳定性在磷酸盐缓冲盐水(PBS)缓冲液和小鼠血清中测试。使用U87Mg细胞进行放射性标记肽的细胞摄取测定。此外,在U87MG携带的小鼠中进行(18)F-FP-3-4A的小动物PET成像和生物分布研究。还通过用封闭肽环(RGDYK)将探针掺入探针来验证放射性标记肽的特异性的受体。我们的研究表明,(18)F-FP-3-4A在PBS缓冲液(pH7.4)和小鼠血清中表现出优异的稳定性。小动物宠物成像和生物分布数据显示(18)F-FP-3-4A表现出快速且良好的肿瘤摄取(3.76±0.59%ID / g,分别为0.5和1 h的2.22±0.62%ID / g)。 (18)F-FP-3-4A从正常组织迅速清除,导致优异的肿瘤至正常组织对比。例如,肝脏吸收仅为0.39±0.07%ID / g,肿瘤与肝比为5.69,1小时P.I.此外,在U87MG异种移植模型中,具有(18)F-FP-3-4A的Cyclo(Rgdyk)的调节(RGDYK)与(18)F-FP-3-4A显着抑制肿瘤摄取(0.41±0.12 Vs 1.02±0.19%Id / g),展示了探针的特定积累在肿瘤中。总之,二价探针(18)F-FP-3-4A的特征在于快速和高肿瘤摄取和优异的肿瘤至正常组织比率。 (18)F-FP-3-4A是一种高度有前途的曲线基的PET探针,用于转化为肿瘤血管生成的临床影像。

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