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体内分子成像探针(18)F-膜联蛋白 B1 用于 PET/CT 检测细胞凋亡:制备与初步评价。

An in vivo molecular imaging probe (18)F-Annexin B1 for apoptosis detection by PET/CT: preparation and preliminary evaluation.

机构信息

PET Center, Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, China.

出版信息

Apoptosis. 2013 Feb;18(2):238-47. doi: 10.1007/s10495-012-0788-0.

Abstract

There is an increasing need to develop non-invasive molecular imaging strategies for visualizing and quantifying apoptosis status of diseases (especially for cancer) for diagnosis and monitoring treatment response. Since externalization of phosphatidylserine (PS) is one of the early molecular events during apoptosis, Annexin B1 (AnxB1), a member of Annexins family with high affinity toward the head group of PS, could be a potential positron emission tomography (PET) imaging probe for imaging cell death process after labeled by positron-emitting nuclides, such as (18)F. In the present study, we investigated a novel PET probe, (18)F-labeled Annexin B1 ((18)F-AnxB1), for apoptosis imaging. (18)F-AnxB1 was prepared reliably by conjugating AnxB1 with a (18)F-tag, N-succinimidyl 4-[(18)F]fluorobenzoate ([(18)F]SFB), in a radiolabeling yield of about 20 % within 40 min. The in vitro binding of (18)F-AnxB1 with apoptotic cells induced by anti-Fas antibody showed twofold increase compared to those without treatment, confirmed by flow cytometric analysis with AnxV-FITC/PI staining. Stability tests demonstrated (18)F-AnxB1 was rather stable in vitro and in vivo without degradation. The serial (18)F-AnxB1 PET/CT scans in healthy rats outlined its biodistribution and pharmacokinetics, indicating a rapid renal clearance and predominant accumulation into kidney and bladder at 2 h p.i. (18)F-AnxB1 PET/CT imaging was successfully applied to visualize in vivo apoptosis sites in tumor induced by chemotherapy and in kidney simulated by ischemia-reperfusion injury. The high-contrast images were obtained at 2 h p.i. to delineate apoptotic tumor. Apoptotic region could be still identified by (18)F-AnxB1 PET 4 h p.i., despite the high probe retention in kidneys. In summary, we have developed (18)F-AnxB1 as a PS-specific PET probe for the apoptosis detection and quantification which could have broad applications from disease diagnosis to treatment monitoring, especially in the cases of cancer.

摘要

目前,人们越来越需要开发非侵入性的分子影像学策略,以可视化和量化疾病(尤其是癌症)的细胞凋亡状态,从而进行诊断和监测治疗反应。由于磷脂酰丝氨酸(PS)的外翻是细胞凋亡过程中的早期分子事件之一,因此 Annexin B1(AnxB1)作为 Annexin 家族的成员,对 PS 的头部基团具有高亲和力,可作为正电子发射断层扫描(PET)成像探针,通过放射性核素(如 18F)进行标记后,对细胞死亡过程进行成像。在本研究中,我们研究了一种新型的 PET 探针,即 18F 标记的 Annexin B1(18F-AnxB1),用于细胞凋亡成像。18F-AnxB1 是通过将 AnxB1 与 18F 标记物,N-琥珀酰亚胺基 4-[[18F] 氟代苯甲酸酯([18F]SFB),在 40 分钟内以约 20%的放射性标记产率可靠地制备的。流式细胞术分析显示,用抗 Fas 抗体诱导的凋亡细胞与 18F-AnxB1 的体外结合比未经处理的细胞增加了两倍,这通过用 AnxV-FITC/PI 染色进行流式细胞术分析得到了证实。稳定性测试表明,18F-AnxB1 在体外和体内均相当稳定,没有降解。健康大鼠的连续 18F-AnxB1 PET/CT 扫描概述了其生物分布和药代动力学,表明在 2 h 时,放射性药物通过肾脏快速清除,主要积聚在肾脏和膀胱中。18F-AnxB1 PET/CT 成像成功地应用于化疗诱导的肿瘤和缺血再灌注损伤模拟的肾脏中体内凋亡部位的可视化。在 2 h 时可以获得高对比度的图像,以描绘凋亡肿瘤。尽管在肾脏中保留了高探针,但在 4 h 时仍可以通过 18F-AnxB1 PET 识别凋亡区域。总之,我们已经开发出 18F-AnxB1 作为 PS 特异性 PET 探针,用于检测和定量细胞凋亡,这可能在疾病诊断到治疗监测等方面具有广泛的应用,尤其是在癌症方面。

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