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Binding and Release of FeIII Complexes from Glucan Particles for the Delivery of T 1 MRI Contrast Agents
Author(s) -
Patel Akanksha,
Asik Didar,
Snyder Eric M.,
Dilillo Alexandra E.,
Cullen Paul J.,
Morrow Janet R.
Publication year - 2020
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.202000003
Subject(s) - chemistry , mri contrast agent , nanoparticle , chelation , biophysics , amphiphile , combinatorial chemistry , nanotechnology , polymer , materials science , organic chemistry , copolymer , biology
Yeast‐derived β‐glucan particles (GPs) are a class of microcarriers under development for the delivery of drugs and imaging agents to immune‐system cells for theranostic approaches. However, the encapsulation of hydrophilic imaging agents in the porous GPs is challenging. Here, we show that the unique coordination chemistry of Fe III ‐based macrocyclic T 1 MRI contrast agents permits facile encapsulation in GPs. Remarkably, GPs labeled with the simple Fe III complexes are stable under physiologically relevant conditions, despite the absence of amphiphilic groups. In contrast to the free Fe III coordination complex, the labeled Fe III ‐GPs have lowered T 1 relaxivity and act as a silenced form of the contrast agent. Addition of a fluorescent tag to the Fe III complex produces a bimodal agent to further enable tracking of the nanoparticles and to monitor release. Treatment of the iron‐labeled GPs with a maltol chelator or with mildly acidic conditions releases the intact iron complex and restores enhanced T 1 relaxation of the water protons.