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Metallofluorocarbon Nanoemulsion for Inflammatory Macrophage Detection via PET and MRI.
Wang, Chao; Leach, Benjamin I; Lister, Deanne; Adams, Stephen R; Xu, Hongyan; Hoh, Carl; McConville, Patrick; Zhang, Jing; Messer, Karen; Ahrens, Eric T.
Afiliación
  • Wang C; Department of Radiology, University of California San Diego, La Jolla, California.
  • Leach BI; Department of Radiology, University of California San Diego, La Jolla, California.
  • Lister D; Department of Radiology, University of California San Diego, La Jolla, California.
  • Adams SR; Department of Pharmacology, University of California San Diego, La Jolla, California.
  • Xu H; Department of Radiology, University of California San Diego, La Jolla, California.
  • Hoh C; Department of Radiology, University of California San Diego, La Jolla, California.
  • McConville P; Department of Radiology, University of California San Diego, La Jolla, California.
  • Zhang J; Invicro, Inc., Boston, Massachusetts; and.
  • Messer K; Moores Cancer Center, University of California San Diego, La Jolla, California.
  • Ahrens ET; Moores Cancer Center, University of California San Diego, La Jolla, California.
J Nucl Med ; 62(8): 1146-1153, 2021 08 01.
Article en En | MEDLINE | ID: mdl-33277399
ABSTRACT
Inflammation is associated with a range of serious human conditions, including autoimmune and cardiovascular diseases and cancer. The ability to image active inflammatory processes greatly enhances our ability to diagnose and treat these diseases at an early stage. We describe molecular compositions enabling sensitive and precise imaging of inflammatory hotspots in vivo.

Methods:

A functionalized nanoemulsion with a fluorocarbon-encapsulated radiometal chelate (FERM) was developed to serve as a platform for multimodal imaging probe development. The 19F-containing FERM nanoemulsion encapsulates 89Zr in the fluorous oil via a fluorinated hydroxamic acid chelate. Simple mixing of the radiometal with the preformed aqueous nanoemulsion before use yields FERM, a stable in vivo cell tracer, enabling whole-body 89Zr PET and 19F MRI after a single intravenous injection.

Results:

The FERM nanoemulsion was intrinsically taken up by phagocytic immune cells, particularly macrophages, with high specificity. FERM stability was demonstrated by a high correlation between the 19F and 89Zr content in the blood (correlation coefficient > 0.99). Image sensitivity at a low dose (37 kBq) was observed in a rodent model of acute infection. The versatility of FERM was further demonstrated in models of inflammatory bowel disease and 4T1 tumor.

Conclusion:

Multimodal detection using FERM yields robust whole-body lesion detection and leverages the strengths of combined PET and 19F MRI. The FERM nanoemulsion has scalable production and is potentially useful for precise diagnosis, stratification, and treatment monitoring of inflammatory diseases.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Macrófagos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Nucl Med Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Macrófagos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Nucl Med Año: 2021 Tipo del documento: Article