High-resolution synchrotron K-edge subtraction CT allows tracking and quantifying therapeutic cells and their scaffold in a rat model of focal cerebral injury and can serve as a reference for spectral photon counting CT.

Q1 Pharmacology, Toxicology and Pharmaceutics
Clément Tavakoli, Elisa Cuccione, Chloé Dumot, Joëlle Balegamire, Salim Aymeric Si-Mohamed, Johoon Kim, Claire Crola-da-Silva, Yves Chevalier, Loïc Boussel, Philippe Douek, David Cormode, Hélène Elleaume, Emmanuel Brun, Marlène Wiart
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引用次数: 0

Abstract

Background: The objective of this study was to demonstrate that synchrotron K-edge subtraction tomography (SKES-CT) can simultaneously track therapeutic cells and their encapsulating carrier, in vivo, in a rat model of focal brain injury using a dual-contrast agent approach. The second objective was to determine if SKES-CT could be used as a reference method for spectral photon counting tomography (SPCCT). Methods: Phantoms containing different concentrations of gold and iodine nanoparticles (AuNPS/INPs) were imaged with SKES-CT and SPCCT to assess their performances. A pre-clinical study was performed in rats with focal cerebral injury which intracerebrally received AuNPs-labelled therapeutic cells encapsulated in a INPs-labelled scaffold. Animals were imaged in vivo with SKES-CT and back-to-back with SPCCT. Results: SKES-CT revealed to be reliable for quantification of gold and iodine, whether alone or mixed. In the preclinical model, SKES-CT showed that AuNPs remained at the site of cell injection, while INPs expanded within and/or along the lesion border, suggesting dissociation of both components in the first days post-administration. Compared to SKES-CT, SPCCT was able to correctly locate gold, but not completely located iodine. When SKES-CT was used as reference, SPCCT gold quantification appeared very accurate both in vitro and in vivo. Iodine quantification by SPCCT was also quite accurate, albeit less so than for gold. Conclusion: We here provide the proof-of-concept that SKES-CT is a novel method of choice for performing dual-contrast agent imaging in the context of brain regenerative therapy. SKES-CT may also serve as ground truth for emerging technologies such as multicolour clinical SPCCT.

Abstract Image

Abstract Image

Abstract Image

高分辨率同步加速器k边减影CT可以对大鼠局灶性脑损伤模型中的治疗细胞及其支架进行跟踪和定量,并可作为光谱光子计数CT的参考。
背景:本研究的目的是证明同步加速器k -边缘减影断层扫描(SKES-CT)可以同时跟踪治疗细胞及其包裹载体,在体内,在局灶性脑损伤大鼠模型中使用双造影剂的方法。第二个目的是确定SKES-CT是否可以作为光谱光子计数层析成像(SPCCT)的参考方法。方法:采用ses - ct和SPCCT对不同浓度的金和碘纳米颗粒(AuNPS/INPs)进行成像,评价其性能。我们在局灶性脑损伤大鼠中进行了临床前研究,在脑内接受了包裹在inps标记支架内的aunps标记的治疗细胞。动物在体内用ses - ct和背靠背用SPCCT成像。结果:无论是单独使用还是混合使用,ses - ct均可可靠地定量测定金和碘。在临床前模型中,sks - ct显示AuNPs保留在细胞注射部位,而INPs在病变边界内和/或沿病变边界扩大,表明在给药后的第一天,这两种成分分离。与sks - ct相比,SPCCT能够正确定位金,但不能完全定位碘。当sks - ct作为参考时,SPCCT金定量在体外和体内都非常准确。SPCCT对碘的定量测定也相当准确,尽管不如对金的定量准确。结论:我们在这里提供了概念证明,sks - ct是在脑再生治疗背景下进行双造影剂成像的一种新方法。sks - ct也可以作为多色临床SPCCT等新兴技术的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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