Kim-1-targeted multimodal nanoprobes for early diagnosis and monitoring of sepsis-induced acute kidney injury

IF 8.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qingjie Chen, Jianbo Yang, Mei Yang, Zhaoxia Luo, Yangyang Lei, Qing Zhang
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Abstract

Sepsis-induced acute kidney injury (AKI) is a critical condition characterized by high mortality and limited early diagnostic tools. This study presents the development of a novel multimodal nanoprobe, 68Ga/99mTc@LTH-SPIONs, for targeted detection and monitoring of sepsis-induced AKI. By combining PET/SPECT imaging capabilities of radiolabeled isotopes (68Ga and 99mTc) with the anatomical resolution of superparamagnetic iron oxide nanoparticles (SPIONs) for MRI, the nanoprobe facilitates precise and non-invasive imaging. Surface modification with the LTH peptide, which specifically targets Kidney Injury Molecule-1 (Kim-1), enhances the nanoprobe’s diagnostic specificity. Extensive in vitro and in vivo evaluations revealed low cytotoxicity, excellent biocompatibility, and effective renal targeting, with metabolites predominantly cleared through urine. In a sepsis AKI mouse model, the nanoprobe provided sensitive and specific imaging, enabling early detection of kidney injury. This study underscores the potential of Kim-1-targeted nanoprobes as a powerful tool for elucidating cellular injury mechanisms and monitoring therapeutic interventions in AKI.

靶向kim -1的多模态纳米探针用于败血症引起的急性肾损伤的早期诊断和监测。
脓毒症引起的急性肾损伤(AKI)是一种以高死亡率和有限的早期诊断工具为特征的危重疾病。本研究提出了一种新型多模态纳米探针,68Ga/99mTc@LTH-SPIONs,用于靶向检测和监测败血症诱导的AKI。通过结合放射性标记同位素(68Ga和99mTc)的PET/SPECT成像能力和超顺磁性氧化铁纳米颗粒(SPIONs)的MRI解剖分辨率,纳米探针有助于精确和非侵入性成像。LTH肽的表面修饰特异性靶向肾损伤分子-1 (Kim-1),增强了纳米探针的诊断特异性。广泛的体外和体内评估显示其细胞毒性低,生物相容性好,有效的肾脏靶向性,代谢物主要通过尿液清除。在脓毒症AKI小鼠模型中,纳米探针提供了敏感和特异性的成像,能够早期发现肾损伤。这项研究强调了kim -1靶向纳米探针作为阐明AKI细胞损伤机制和监测治疗干预措施的有力工具的潜力。
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
Apoptosis
Apoptosis 生物-生化与分子生物学
CiteScore
9.10
自引率
4.20%
发文量
85
审稿时长
1 months
期刊介绍: Apoptosis, a monthly international peer-reviewed journal, focuses on the rapid publication of innovative investigations into programmed cell death. The journal aims to stimulate research on the mechanisms and role of apoptosis in various human diseases, such as cancer, autoimmune disease, viral infection, AIDS, cardiovascular disease, neurodegenerative disorders, osteoporosis, and aging. The Editor-In-Chief acknowledges the importance of advancing clinical therapies for apoptosis-related diseases. Apoptosis considers Original Articles, Reviews, Short Communications, Letters to the Editor, and Book Reviews for publication.
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