A stable, highly concentrated fluorous nanoemulsion formulation for in vivo cancer imaging via 19F-MRI

被引:1
|
作者
Heaton, Alexa R. [1 ]
Lechuga, Lawrence M. [2 ]
Tangsangasaksri, Montira [3 ]
Ludwig, Kai D. [2 ]
Fain, Sean B. [2 ,4 ]
Mecozzi, Sandro [1 ,3 ,5 ]
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Med Phys, Madison, WI 53705 USA
[3] Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
[4] Univ Iowa, Dept Radiol, Iowa City, IA USA
[5] Univ Wisconsin, Sch Pharm, Pharmaceut Sci Div, 777 Highland Ave, Madison, WI 53705 USA
基金
美国国家卫生研究院;
关键词
F-19-MRI; cancer diagnostics; fluorous nanoemulsion; perfluoro-[15-crown-5]-ether; semifluorinated polymers; ENHANCED PERMEABILITY; CONTRAST AGENTS; MRI; CHEMISTRY; PERFLUOROCARBONS; RETENTION; TOXICITY; CELLS; TUMOR; NANOPARTICLES;
D O I
10.1002/nbm.5100
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Magnetic resonance imaging (MRI) is a routine diagnostic modality in oncology that produces excellent imaging resolution and tumor contrast without the use of ionizing radiation. However, improved contrast agents are still needed to further increase detection sensitivity and avoid toxicity/allergic reactions associated with paramagnetic metal contrast agents, which may be seen in a small percentage of the human population. Fluorine-19 (F-19)-MRI is at the forefront of the developing MRI methodologies due to near-zero background signal, high natural abundance of 100%, and unambiguous signal specificity. In this study, we have developed a colloidal nanoemulsion (NE) formulation that can encapsulate high volumes of the fluorous MRI tracer, perfluoro-[15-crown-5]-ether (PFCE) (35% v/v). These nanoparticles exhibit long-term (at least 100 days) stability and high PFCE loading capacity in formulation with our semifluorinated triblock copolymer, M2F8H18. With sizes of approximately 200 nm, these NEs enable in vivo delivery and passive targeting to tumors. Our diagnostic formulation, M2F8H18/PFCE NE, yielded in vivo F-19-MR images with a high signal-to-noise ratio up to 100 in a tumor-bearing mouse model at clinically relevant scan times. M2F8H18/PFCE NE circulated stably in the vasculature, accumulated in high concentration of an estimated 4-9 x 10(17 19)F spins/voxel at the tumor site, and cleared from most organs over the span of 2 weeks. Uptake by the mononuclear phagocyte system to the liver and spleen was also observed, most likely due to particle size. These promising results suggest that M2F8H18/PFCE NE is a favorable F-19-MR diagnostic tracer for further development in oncological studies and potential clinical translation.
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页数:14
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