1. CT and CEST MRI bimodal imaging of the intratumoral distribution of iodinated liposomes
- Author
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Shibin Zhou, Kannie W. Y. Chan, Raag D. Airan, Zelong Chen, Michael T. McMahon, Peter C.M. van Zijl, Yuguo Li, Jiadi Xu, Guanshu Liu, Yikai Xu, Zheng Han, and Jeff W.M. Bulte
- Subjects
Biodistribution ,Liposome ,business.industry ,Cest mri ,Iodixanol ,030218 nuclear medicine & medical imaging ,Rhodamine ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,chemistry ,In vivo ,030220 oncology & carcinogenesis ,Drug delivery ,medicine ,Distribution (pharmacology) ,Radiology, Nuclear Medicine and imaging ,Original Article ,Nuclear medicine ,business ,medicine.drug - Abstract
Background To develop liposomes loaded with iodinated agents as nanosized CT/MRI bimodal contrast agents for monitoring liposome-mediated drug delivery. Methods Rhodamine-labeled iodixanol (VisipaqueTM)-loaded liposomes (IX-lipo) were prepared and tested for their properties as a diamagnetic CEST contrast agent in vitro. Mice bearing subcutaneous CT26 colon tumors were injected i.v. with 1 g/kg (535 mg iodine/kg) IX-lipo, and in vivo CT and CEST MR images were acquired on day 3. CT and CEST MR images were also acquired for tumor-bearing mice co-injected with IX-lipo and tumor necrosis factor (TNF-α). Results In addition to CT contrast, IX-lipo exhibited a strong CEST contrast similar to its non-liposomal form, with a detectability of ~2 nM per liposome. Both CT imaging and CEST MRI showed that i.v. injection of IX-lipo resulted in a rim enhancement of CT26 tumors with a heterogeneous central distribution. In contrast, co-injection of TNF-α caused a significantly augmented CT/MRI contrast in the tumor center. The intratumoral biodistribution of IX-lipo correlated well to the rhodamine patterns observed with fluorescence microscopy. Conclusions We have developed a CT/MRI bimodal imaging approach for monitoring the delivery and biodistribution of liposomes by loading them with the clinically approved X-ray/CT contrast agent iodixanol. Our approach may be easily adapted for other-FDA approved iodinated agents and thus has great translational potential.
- Published
- 2019