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镓-68 标记的泛菌衍生八肽作为一种有潜力的感染显像剂。

Gallium-68 labeled Ubiquicidin derived octapeptide as a potential infection imaging agent.

机构信息

Radiopharmaceuticals Division, Bhabha Atomic Research Centre (BARC), Mumbai 400085, India; Homi Bhabha National Institute, Anushaktinagar, Mumbai 400094, India.

Radiopharmaceuticals Division, Bhabha Atomic Research Centre (BARC), Mumbai 400085, India; Homi Bhabha National Institute, Anushaktinagar, Mumbai 400094, India.

出版信息

Nucl Med Biol. 2018 Jul-Aug;62-63:47-53. doi: 10.1016/j.nucmedbio.2018.04.003. Epub 2018 May 4.

Abstract

INTRODUCTION

Gallium-68 based infection imaging agents are in demand to detect infection foci with high spatial resolution and sensitivity. In this study, Ubiquicidin derived octapeptide, UBI (31-38) conjugated with macrocyclic chelator NOTA was radiolabeled with Ga to develop infection imaging agent.

METHODS

Circular dichroism (CD) spectroscopy was performed to study conformational changes in UBI (31-38) and its NOTA conjugate in a "membrane like environment". Radiolabeling of NOTA-UBI (31-38) with Ga was optimized and quality control analysis was done by chromatography techniques. In vitro evaluation of Ga-NOTA-UBI (31-38) in S. aureus and preliminary biological evaluation in animal model of infection was studied. Initial clinical evaluation in three patients with suspected infection was carried out.

RESULTS

Ga-NOTA-UBI (31-38) was prepared in high radiochemical yields and high radiochemical purity. In vitro evaluation of Ga-NOTA-UBI (31-38) complex in S. aureus confirmed specificity of the agent for bacteria. Biodistribution studies with Ga-NOTA-UBI (31-38) revealed specific uptake of the complex in infected muscle compared to inflamed muscle with T/NT ratio of 3.24 ± 0.7 at 1 h post-injection. Initial clinical evaluation in two patients with histopathologically confirmed infective foci conducted after intravenous injection of 130-185 MBq of Ga-NOTA-UBI (31-38) and imaging at 45-60 min post-injection revealed specific uptake at the sites of infection and clearance from vital organs. No uptake of tracer was observed in suspected infection foci in one patient, which was proven to be aseptic and served as negative control.

CONCLUSION

This is the first report on Ga labeled NOTA-UBI (31-38) fragment for prospective infection imaging.

摘要

简介

镓-68 基感染显像剂的需求很高,需要具有高空间分辨率和灵敏度来检测感染灶。在这项研究中,尿抑胃素衍生的八肽 UBI(31-38)与大环螯合剂 NOTA 连接,并用 Ga 标记开发感染显像剂。

方法

圆二色性(CD)光谱用于研究 UBI(31-38)及其 NOTA 缀合物在“类似膜的环境”中的构象变化。优化了 NOTA-UBI(31-38)与 Ga 的放射性标记,并通过色谱技术进行质量控制分析。研究了 Ga-NOTA-UBI(31-38)在金黄色葡萄球菌中的体外评价和感染动物模型中的初步生物学评价。对三名疑似感染患者进行了初步临床评价。

结果

Ga-NOTA-UBI(31-38)以高放射化学产率和高放射化学纯度制备。Ga-NOTA-UBI(31-38)复合物在金黄色葡萄球菌中的体外评价证实了该药物对细菌的特异性。Ga-NOTA-UBI(31-38)的生物分布研究显示,与炎症肌肉相比,感染肌肉中的复合物特异性摄取,注射后 1 小时 T/NT 比值为 3.24±0.7。对两名经组织病理学证实感染灶的患者进行了初步临床评价,静脉注射 130-185 MBq Ga-NOTA-UBI(31-38)后进行成像,注射后 45-60 分钟,在感染部位特异性摄取并从重要器官清除。在一名疑似感染灶的患者中未观察到示踪剂摄取,该患者被证实为无菌性,作为阴性对照。

结论

这是首次报道镓标记的 NOTA-UBI(31-38)片段用于前瞻性感染成像。

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