[68Ga]Ga-Schizokinen,一种用于选择性细菌感染成像的潜在放射性示踪剂。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-08-09 Epub Date: 2024-07-16 DOI:10.1021/acsinfecdis.4c00067
Asma Akter, George Firth, Afnan M F Darwesh, Margaret S Cooper, Hataichanok Chuljerm, Agostino Cilibrizzi, Philip J Blower, Robert C Hider, Oliver Lyons, Silke Schelenz, Varun Mehra, Vincenzo Abbate
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引用次数: 0

摘要

镓-68标记的嗜苷酸作为放射性示踪剂,在开发原位感染特异性成像诊断方面受到了广泛关注。在这里,我们报告了镓-68标记的五味子宁([68Ga]Ga-SKN)的放射性标记、体外筛选和体内药代动力学(PK),将其作为一种新的潜在放射性示踪剂用于细菌感染成像。我们放射性标记的SKN放射化学纯度≥95%。我们的体外研究证明了它的亲水性、中性pH值稳定性、在人血清中的短期稳定性和转切性。大肠杆菌、铜绿假单胞菌、金黄色葡萄球菌和表皮葡萄球菌对[68Ga]Ga-SKN的体外摄取,而白色念珠菌、白僵菌或曲霉菌则没有摄取,这证明了它对细菌物种的特异性。在健康小鼠体内进行的全身[68Ga]Ga-SKN正电子发射断层扫描(PET)与计算机断层扫描(CT)相结合的结果表明,[68Ga]Ga-SKN可迅速排出肾脏,没有或只有极少的器官摄取。随后的体内外生物分布与这种快速 PK 相似,肾脏排泄迅速,血液潴留极少,无主要器官摄取,并且在注射后 60 分钟后显示示踪剂在尿液中有一些解离。这些研究结果证明,[68Ga]Ga-SKN 作为细菌特异性放射性示踪剂用于感染成像值得进一步评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[<sup>68</sup>Ga]Ga-Schizokinen, a Potential Radiotracer for Selective Bacterial Infection Imaging.

[68Ga]Ga-Schizokinen, a Potential Radiotracer for Selective Bacterial Infection Imaging.

Gallium-68-labeled siderophores as radiotracers have gained interest for the development of in situ infection-specific imaging diagnostics. Here, we report radiolabeling, in vitro screening, and in vivo pharmacokinetics (PK) of gallium-68-labeled schizokinen ([68Ga]Ga-SKN) as a new potential radiotracer for imaging bacterial infections. We radiolabeled SKN with ≥95% radiochemical purity. Our in vitro studies demonstrated its hydrophilic characteristics, neutral pH stability, and short-term stability in human serum and toward transchelation. In vitro uptake of [68Ga]Ga-SKN by Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and S. epidermidis, but no uptake by Candida glabrata, C. albicans, or Aspergillus fumigatus, demonstrated its specificity to bacterial species. Whole-body [68Ga]Ga-SKN positron emission tomography (PET) combined with computerized tomography (CT) in healthy mice showed rapid renal excretion with no or minimal organ uptake. The subsequent ex vivo biodistribution resembled this fast PK with rapid renal excretion with minimal blood retention and no major organ uptake and showed some dissociation of the tracer in the urine after 60 min postinjection. These findings warrant further evaluation of [68Ga]Ga-SKN as a bacteria-specific radiotracer for infection imaging.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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