MRI Capable Theranostic Agents
Hui Mao1

1Department of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, GA, United States

Synopsis

New generation magnetic resonance imaging (MRI) contrast agents such as nanoparticles can be developed as theranostic agents which integrate the MRI contrast enhancing capability with therapeutic functions. The objective of this lecture is to give the audience an update of the recent developments in MRI enabled theranostics and stimulate the interests and new ideas to further advance the research and clinical translations of MRI enabled theranostics. The rational design of MRI capable theranostics agents, approaches for making the desired theranostic platforms, and MRI methods developed to enable MRI visualization of delivery processes will be discussed and presented with examples.

Theranostics & Novel Molecular Probes

Various classes of new generation magnetic resonance imaging (MRI) contrast agents such as nanoparticles have potential to be developed as theranostic agents which integrate the MRI contrast enhancing capability with therapeutic functions [1-2]. These theranostic MRI contrast agents can be used for targeted delivery of therapeutics while using MRI to track, or even quantify, the distribution, accumulation and clearance of the agents noninvasively in preclinical animal models or patients, and subsequently to monitor the treatment responses [3-4]. With MRI widely available and typical need of relatively large dosages of low toxicity MRI contrast agents, well-engineered MRI based theranostics has advantages in targeting, improved pharmacokinetics and more importantly allowing for “seeing and believing” the delivery of the agents. On the other hand, MRI based theranostics has expanded MRI from traditional diagnostic applications to image-guided therapy applications, increasing the value of MRI in healthcare research and delivery. The emerging field of theranostics is highly interdisciplinary and attracts a wide range of scientific and engineering expertise, including chemistry, biomaterials, pharmacology, imaging sciences and technology, as well as clinical specialties that can apply image-guided treatments. To those who are interested in working in the field, this lecture attempts to introduce the general concept and rational design of the theranostics agents, chemical and biological properties needed in a theranostics agent, strategies for properly loading and releasing the therapeutics, approaches for delivery of theranostics and some examples of MRI capable theranostic platforms (shown in Figure) that have been developed for MRI and drug delivery[5-6], specifically superparamagnetic iron oxide nanoparticles (SPIO or IONP) which have been used in clinical applications. Complementary to the material development, MRI methods that have been developed and applied to enable MRI contrast enhancement and visualization of delivery processes in vivo will be presented. The lecture will also discuss current challenges in developing and applying theranostics platform, for example, delivery efficiency, molecular targeting, image quantification, and biocompatibility and clearance of theranostics agents [7-8]. The objective of this lecture is to give the audience an update of the recent developments in MRI capable theranostics and stimulate the interests and new ideas to further advance the research and clinical translations of theranostics that is facilitated by the power of MRI technology.

Acknowledgements

No acknowledgement found.

References

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Figures

Targeted delivery of chemotherapy agent gemcitabine (Gem) with iron oxide nanoparticle (IONP) in a pancreatic cancer mouse model. A. Design of enzymatic activated release of drug using a cleavable peptide GFLG-Gem conjugates linked on IONP (IONP-Gem); B. Targeting and accumulation of the drug loading IONPs can be detected by optical imaging, T2 weighted MRI (signal drop) and ultra-short TE or UTE MRI (signal enhancement); C. Tumor responses to different forms of delivery shows targeted delivery using IONP exhibiting the most significant inhibition of tumor growth; D. Tumor volumes in responding to different treatments are monitored and measured non-invasively by MRI.

Proc. Intl. Soc. Mag. Reson. Med. 26 (2018)