{"title":"Biologically inspired bimodal imaging agent incorporating quantum dots and magnetic nanoparticles targeting tumor angiogenesis","authors":"Qi Guo, Menglin Wu, Jiang Li, Guoping Xu, Xinhong Wu, Xiudi Lu, Xunxiao Zhao, Guilai Li, Xuening Zhang, Xue Li, Yang Zhao","doi":"10.1007/s11051-026-06648-4","DOIUrl":null,"url":null,"abstract":"<div><p>Angiogenesis is an early marker of tumor growth, and a key process that promotes tumor growth, progression and metastasis. Accurate and early evaluation of tumor angiogenic activity using non-invasive imaging modalities is crucial for tumor diagnosis, therapeutic monitoring, and prognosis prediction. In this study, we reported a sensitive, specific, and biocompatible magnetic resonance (MR)/ fluorescence (FL) bimodal contrast agent for targeting aminopeptidase-N (APN/CD13) overexpressed in tumor angiogenesis. The obtained cNpQDs exhibited potent T1-weighted imaging capabilities (r<sub>1</sub> = 11.1081 mM<sup>−1</sup>·s<sup>−1</sup>) and effective photoluminescence emission. The CD13 binding affinity of the peptide cNGR was evaluated using a HUVEC cell-based receptor binding test, in which the internalization rate of cNpQDs was 10.17 times higher than that of pQDs. Furthermore, in vivo experiments indicated that MR/FL imaging of cNpQDs significantly enhanced the contrast of tumor angiogenesis. Biocompatibility studies provide evidence that cNpQDs has no obvious toxicity in vivo. These findings indicated that cNpQDs may serve as an efficiency MR/FL bimodal contrast agent, offering a potential alternative for assessing tumor angiogenesis.</p></div>","PeriodicalId":653,"journal":{"name":"Journal of Nanoparticle Research","volume":"28 5","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2026-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nanoparticle Research","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s11051-026-06648-4","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Angiogenesis is an early marker of tumor growth, and a key process that promotes tumor growth, progression and metastasis. Accurate and early evaluation of tumor angiogenic activity using non-invasive imaging modalities is crucial for tumor diagnosis, therapeutic monitoring, and prognosis prediction. In this study, we reported a sensitive, specific, and biocompatible magnetic resonance (MR)/ fluorescence (FL) bimodal contrast agent for targeting aminopeptidase-N (APN/CD13) overexpressed in tumor angiogenesis. The obtained cNpQDs exhibited potent T1-weighted imaging capabilities (r1 = 11.1081 mM−1·s−1) and effective photoluminescence emission. The CD13 binding affinity of the peptide cNGR was evaluated using a HUVEC cell-based receptor binding test, in which the internalization rate of cNpQDs was 10.17 times higher than that of pQDs. Furthermore, in vivo experiments indicated that MR/FL imaging of cNpQDs significantly enhanced the contrast of tumor angiogenesis. Biocompatibility studies provide evidence that cNpQDs has no obvious toxicity in vivo. These findings indicated that cNpQDs may serve as an efficiency MR/FL bimodal contrast agent, offering a potential alternative for assessing tumor angiogenesis.
期刊介绍:
The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size.
Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology.
The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.