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首页> 外文期刊>ACS Omega >Preclinical Evaluation of a Novel 99mTc-Labeled CB86 for Rheumatoid Arthritis Imaging
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Preclinical Evaluation of a Novel 99mTc-Labeled CB86 for Rheumatoid Arthritis Imaging

机译:用于类风湿性关节炎成像的新型99MTC标记CB86的临床前评价

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摘要

Early diagnosis and therapy are crucial to control disease progression optimally and achieve a good prognosis in rheumatoid arthritis (RA). Previous study showed that a technetium-99m (~(99m)Tc)-labeled TSPO ligand (~(99m)Tc-CB256 [2-(8-(2-(bis(pyridin-2-yl)methyl)amino)acetamido)-2-(4-chlorophenyl)H -imidazo[1,2-a ]pyridin-3-yl)-N ,N -dipropylacetamide] composed of a translocator protein (TSPO) ligand CB86 [[2-(4-chlorophenyl)-8-amino-imidazo[1,2-a ]-pyridin-3-yl]-N ,N -di-n -propylacetamide] and di-(2-picolyl)amine, a bifunctional chelate agent, was used to image a TSPO-rich cancer cell in vitro ; however, few ~(99m)Tc-CB256 in vivo evaluation has been reported so far probably due to the cytotoxicity of CB256 (ca . 75 times more than analogous CB86). Herein, we describe a novel TSPO targeting radiopharmaceutical consisting of CB86 and diethylenetriaminepentaacetic acid (DTPA), a conventional bifunctional chelating ligand in clinical trials used to prepare ~(99m)Tc-labeled CB86, and its evaluation as a ~(99m)Tc-single-photon emission computed tomography (SPECT) probe. The radiosynthesis and characterization of ~(99m)Tc-DPTA-CB86 including hydrophilicity and stability tests were determined. Additionally, the binding affinity and specificity of ~(99m)Tc-DTPA-CB86 to TSPO were evaluated using RAW264.7 macrophage cells. Biodistribution and ~(99m)Tc-SPECT studies were conducted on rheumatoid arthritis (RA) rat models after the injection of ~(99m)Tc-DTPA-CB86 with or without co-injection of unlabeled DTPA-CB86. The radiosynthesis of ~(99m)Tc-DTPA-CB86 was completed successfully with the labeling yields and radiochemical purity of 95.86 ± 2.45 and 97.45 ± 0.69%, respectively. The probe displayed good stability in vitro and binding specificity to RAW264.7 macrophage cells. In the biodistribution studies, ~(99m)Tc-DTPA-CB86 exhibited rapid inflammatory ankle accumulation. At 180 min after administration, ~(99m)Tc-DTPA-CB86 uptakes of the left inflammatory ankle were 2.35 ± 0.10 percentage of the injected radioactivity per gram of tissue (% ID/g), significantly higher than those of the normal tissues. ~(99m)Tc-SPECT imaging studies revealed that ~(99m)Tc-DTPA-CB86 could clearly identify the left inflammatory ankle with good contrast at 30–180 min after injection. Therefore, ~(99m)Tc-DTPA-CB86 may be a promising probe for arthritis ~(99m)Tc-SPECT imaging.
机译:早期诊断和治疗对于对疾病进行最佳的进展至关重要,并达到类风湿性关节炎(RA)的良好预后。先前的研究表明,施工-99M(〜(99m)Tc) - 标记的Tspo配体(〜(99m)Tc-Cb256 [2-(2-(二甲基-2-基)甲基)氨基)乙酰氨基)-2-(4-氯苯基) H-Imidazo [1,2- N-二丙基乙酰胺]组成( TSPO)配体CB86 [[2-(4-氯苯基)-8-氨基 - 咪唑[1,2- A] - 吡啶-3-基] - N, N -DI- < i> N-丙基乙酰胺]和二(2-吡酰基)胺,双官能螯合物剂,用于在体外成像富含Tspo的癌细胞;然而,迄今为止,迄今为止,迄今为止,几乎(99米)TC-CB256 可能是由于CB256的细胞毒性( Ca.比类似CB86多的35倍)的细胞毒性。在此,我们描述了一种新的TSPO靶向放射性药物,其由CB86和二亚乙基三胺乙酸(DTPA)组成,临床试验中的常规双官能螯合配体,用于制备〜(99m)的TC标记的CB86,其评价为〜(99M)TC-单光子发射计算断层扫描(SPECT)探针。确定了〜(99M)TC-DPTA-CB86的可辐射合成和表征,包括亲水性和稳定性试验。另外,使用Raw264.7巨噬细胞评估〜(99M)TC-DTPA-CB86至TSPO的结合亲和力和特异性。生物分布和〜(99米)TC-SPECT研究是在注射〜(99m)TC-DTPA-CB86后的类风湿性关节炎(RA)大鼠模型上进行或不注重未标记的DTPA-CB86。 〜(99m)TC-DTPA-CB86的可热化合成成功完成,标记产率和放射化学纯度分别为95.86±2.45和97.45±0.69%。探针显示出良好的稳定性对Raw264.7巨噬细胞的体外和结合特异性。在生物分布研究中,〜(99米)TC-DTPA-CB86表现出快速的炎症踝堆积。在给药后180分钟,左炎踝的〜(99米)TC-DTPA-CB86摄取为每克组织(%ID / G)的注射放射性2.35±0.10百分比,显着高于正常组织的放射性。 〜(99米)TC-SPECT成像研究表明,〜(99米)TC-DTPA-CB86可以在注射后30-180分钟的30-180分钟明确鉴定左炎症踝。因此,〜(99m)TC-DTPA-CB86可以是关节炎〜(99M)TC-SPECT成像的有希望的探针。

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