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      Polymeric 19F MRI agents responsive to reactive oxygen species

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          Abstract

          Medical imaging agents that can report on the biological state are attracting increasing interest.

          Abstract

          Medical imaging agents that can report on the biological state are attracting increasing interest. Here we report the development of novel 19F polymeric imaging agents that are activated by reactive oxygen species (ROS). The imaging agents composed of thioether- and fluorine-containing methacrylate monomers were synthesised using atom transfer radical polymerisation (ATRP) from a hydrophilic poly(ethylene glycol)-based initiator. In aqueous solution, the agents self-assemble into nanoparticles with compact hydrophobic cores. The mobility of the fluorinated segments within the cores is greatly restricted, thereby significantly shortening the 19F T 2 relaxation times and attenuating the 19F NMR signal. However, upon treatment with ROS ( i.e. H 2O 2), the hydrophobic thioether groups of the agents are oxidised to hydrophilic sulfoxide groups, resulting in the disassembly of the aggregated nanoparticles. The disassembly of the 19F MRI agents lengthens the T 2 relaxation times, and enables an appreciable enhancement of 19F NMR signal. 19F MRI of solutions of the polymers before and after oxidation demonstrated a remarkable “OFF–ON” regulation in response to ROS. The sensitivity of the imaging agents was further enhanced by adding a pH switch, resulting in a ROS/pH dual-responsive 19F MRI agent. The most pronounced change in intensity of the 19F NMR/MRI signal was achieved in response to the presence of ROS in a mildly acidic environment. The work demonstrates that these novel polymeric 19F MRI agents hold great potential for improved diagnosis and therapy of diseases presenting high levels of ROS.

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          Most cited references43

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          Biocompatible polymeric nanoparticles degrade and release cargo in response to biologically relevant levels of hydrogen peroxide.

          Oxidative stress is caused predominantly by accumulation of hydrogen peroxide and distinguishes inflamed tissue from healthy tissue. Hydrogen peroxide could potentially be useful as a stimulus for targeted drug delivery to diseased tissue. However, current polymeric systems are not sensitive to biologically relevant concentrations of H(2)O(2) (50-100 μM). Here we report a new biocompatible polymeric capsule capable of undergoing backbone degradation and thus release upon exposure to such concentrations of hydrogen peroxide. Two polymeric structures were developed differing with respect to the linkage between the boronic ester group and the polymeric backbone: either direct (1) or via an ether linkage (2). Both polymers are stable in aqueous solution at normal pH, and exposure to peroxide induces the removal of the boronic ester protecting groups at physiological pH and temperature, revealing phenols along the backbone, which undergo quinone methide rearrangement to lead to polymer degradation. Considerably faster backbone degradation was observed for polymer 2 over polymer 1 by NMR and GPC. Nanoparticles were formulated from these novel materials to analyze their oxidation triggered release properties. While nanoparticles formulated from polymer 1 only released 50% of the reporter dye after exposure to 1 mM H(2)O(2) for 26 h, nanoparticles formulated from polymer 2 did so within 10 h and were able to release their cargo selectively in biologically relevant concentrations of H(2)O(2). Nanoparticles formulated from polymer 2 showed a 2-fold enhancement of release upon incubation with activated neutrophils, while controls showed a nonspecific response to ROS producing cells. These polymers represent a novel, biologically relevant, and biocompatible approach to biodegradable H(2)O(2)-triggered release systems that can degrade into small molecules, release their cargo, and should be easily cleared by the body.
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            Characteristics of gadolinium-DTPA complex: a potential NMR contrast agent.

            Chelation of the rare-earth element gadolinium (Gd) with diethylenetriaminepentaacetic acid (DTPA) results in a strongly paramagnetic, stable complex that is well tolerated in animals. The strongly paramagnetic gadolinium complex reduces hydrogen-proton relaxation times even in low concentrations (less than 0.01 mmol/L). The pharmacokinetic behavior of intravenously delivered Gd-DTPA is similar to the well known iodinated contrast agents used in urography and angiography; excretion is predominantly through the kidneys with greater than 90% recovery in 24 hr. The intravenous LD50 of the meglumine salt of Gd-DTPA is 10 mmol/kg for the rat; in vivo there is no evidence of dissociation of the gadolinium ion from the DTPA ligand. The combination of strong proton relaxation, in-vivo stability, rapid urinary excretion, and high tolerance favors the further development and the potential clinical application of gadolinium-DTPA as a contrast enhancer in magnetic resonance imaging.
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              Superparamagnetic iron oxide nanoparticles: from preparations to in vivo MRI applications

                Author and article information

                Journal
                PCOHC2
                Polymer Chemistry
                Polym. Chem.
                Royal Society of Chemistry (RSC)
                1759-9954
                1759-9962
                2017
                2017
                : 8
                : 31
                : 4585-4595
                Affiliations
                [1 ]Australian Institute for Bioengineering and Nanotechnology
                [2 ]The University of Queensland
                [3 ]Brisbane
                [4 ]Australia
                [5 ]ARC Centre of Excellence in Convergent Bio-Nano Science and Technology
                Article
                10.1039/C7PY00986K
                2414fd50-eeaf-40b0-aa22-9f1e46757038
                © 2017
                History

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