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Magnetic Resonance Materials in Physics, Biology and Medicine

Erschienen in:

Open Access 29.11.2018 | Review

Fluorine polymer probes for magnetic resonance imaging: quo vadis?

verfasst von: Daniel Jirak, Andrea Galisova, Kristyna Kolouchova, David Babuka, Martin Hruby

Erschienen in: Magnetic Resonance Materials in Physics, Biology and Medicine | Ausgabe 1/2019

Abstract

Over the last few years, the development and relevance of ¹⁹F magnetic resonance imaging (MRI) for use in clinical practice has emerged. MRI using fluorinated probes enables the achievement of a specific signal with high contrast in MRI images. However, to ensure sufficient sensitivity of ¹⁹F MRI, fluorine probes with a high content of chemically equivalent fluorine atoms are required. The majority of ¹⁹F MRI agents are perfluorocarbon emulsions, which have a broad range of applications in molecular imaging, although the content of fluorine atoms in these molecules is limited. In this review, we focus mainly on polymer probes that allow higher fluorine content and represent versatile platforms with properties tailorable to a plethora of biomedical in vivo applications. We discuss the chemical development, up to the first imaging applications, of these promising fluorine probes, including injectable polymers that form depots that are intended for possible use in cancer therapy.

ATRP

Atom transfer polymerization

CPT

Cloud point temperature

CryoTEM

Transmission electron cryomicroscopy

DCs

Dendritic cells

DEAMA

2-(N,N-Diethylamino)ethyl methacrylate

DLS

Dynamic light scattering

DMSO

Dimethyl sulfoxide

EPR

Enhanced permeability and retention effect

LCST

Lower critical solution temperature

MRI

Magnetic resonance imaging

OFPMA

Octafluoropentyl methacrylate

PBS

Phosphate-buffered saline

PDEA

Poly[2-(N,N-diethylamino)ethyl methacrylate]

PDFEA

Poly[N-(2,2-difluorethyl)acrylamide]

PDMAEMA

Poly[2-(N,N-dimethylamino)ethyl methacrylate]

PDMS

Polydimethylsiloxanes

PEO

Poly(ethylene oxide)

PEOMA

PEO monomethylether methacrylate

PERFECTA

Superfluorinated probe

PFC

Perfluorocarbon

PFCE

Perfluoro-15-crown-5-ether

PFS

2,3,4,5,6-Pentafluorostyrene

PFOB

Perfluorooctyl bromide

poly(OEGA)m-PFPE

Oligo(ethylene glycol) methyl ether acrylate

PFPE

Perfluoropolyethers

PHPMA

Poly[N-(2-hydroxypropyl)methacrylamide]

PMeOx

Poly(2-methyl-2-oxazoline)

RAFT

Reversible addition fragmentation chain transfer

Radiofrequency

ROS

Reactive oxygen species

SNR

Signal-to-noise ratio

TFEA

2,2,2-Trifluorethylacrylate

TFEMA

2,2,2-Trifluorethyl methacrylate

UTE

Ultrashort echo time

ZTE

Zero echo time

Introduction

Magnetic resonance imaging (MRI) using fluorinated probes (¹⁹F MRI) enables high contrast in images due to the negligible fluorine background of living tissues. For this reason, fluorine isotopes are visualized with high specificity, allowing for so-called “hot spot” imaging where the ¹⁹F MR signal is overlaid on a proton reference MR image. Moreover, the fluorine isotope ¹⁹F resonates at a Larmor frequency close to that of the proton ¹H (94% of ¹H); therefore, the hardware used for ¹H MR imaging, with minor modifications, can also be used for ¹⁹F MRI. Currently, many clinical and experimental scanners have become available for hardware modifications and the use of appropriate radiofrequency (RF) coils. Usually, the RF coils intended for ¹⁹F MR are constructed to be dual-tuned for both ¹H/¹⁹F MRI. The ¹⁹F MR signal is proportional to the number of ¹⁹F nuclei, which allows absolute quantification of the ¹⁹F content.

For ¹⁹F MRI, fluorine-containing probes need to be synthesized and then administered into the organism by either injection (intravenously or locally to the site of interest) or exogenous labeling of cells. Currently, there is a wide range of available fluorine probes for experimental and even clinical applications summarized in many excellent reviews [1‐4]. The implementation of ¹⁹F MR probes ranges from cell targeting [5‐8] and in vivo tracking of labeled cells [9‐18], cancer diagnosis [19‐22], inflammation monitoring [23‐26], amyloid plaque detection or suppression [27‐29], in situ partial oxygen pressure (pO₂) determination [30, 31], drug metabolism (e.g., of 5-fluorouracil) investigation [32], intra/extracellular pH measurement [33, 34] or cation concentration estimation in cells and tissues [35]. In humans, the ¹⁹F probes have been tested in the immunotherapy of colorectal cancer with labeled dendritic cells, and a number of other clinical trials are ongoing [3, 12]. Currently, several theranostic ¹⁹F MR probes combining both diagnosis and therapy [36] have been implemented; however, testing of the probes on biological models of diseases is far behind their constantly evolving chemical development.

The main drawback of ¹⁹F MR imaging is its low sensitivity due to the low amount of ¹⁹F nuclei per molecule of the synthesized fluorine-based probes. Usually, the concentration of ¹⁹F atoms in fluorine-based probes is in the millimolar range (for comparison, water has a proton concentration of approximately 110 M under ambient conditions); therefore, agents containing a large number of ¹⁹F atoms are necessary for a sufficiently high signal-to-noise ratio (SNR). For a well-resolved single spectral peak, the key property needed for fluorine probes is an as-high-as-possible fraction of chemically equivalent ¹⁹F atoms in the molecule. A single peak allows us to detect a higher ¹⁹F MR signal compared to multiple spectral peaks, which can cause chemical shift artifacts in the MR images.

These demands can be accomplished, e.g., by probes based on polymer structures. Polymer probes enable the incorporation of a large amount of chemically equivalent fluorine atoms into a single molecule and thus could overcome the sensitivity issue of ¹⁹F MRI. Moreover, polymer probes can be easily modified to increase their biological response and improve their behavior in living systems (pH, thermoresponsive parts or bonds, which might be enzymatically degraded) or to add the imaging labels to drug moieties. In this review, we summarize the current state of the art for polymer-based ¹⁹F MRI probes that have great potential in human medicine.

Types of fluorine-containing probes

Various types of fluorinated agents are available in the form of fluorinated perfluorocarbon (PFC) nanoemulsions [37], fluorinated lanthanide chelates [2, 6], fluorinated nucleotides [32], fluoride-based nanocrystals [38], multicompartment amphiphilic polymers [19, 39‐41], etc. A brief overview of fluorine-containing probes, including their systematic names, abbreviations, chemical structures, molecular weights and fluorine content, can be found in Table 1.

Table 1

Overview of the most commonly used fluorine-containing probes

https://static-content.springer.com/image/art%3A10.1007%2Fs10334-018-0724-6/MediaObjects/10334_2018_724_Tab1_HTML.png

The most frequently used ¹⁹F MR agents are liquid PFCs, e.g., perfluoro-15-crown-5-ether (PFCE) (containing 20 fluorine atoms), perfluorooctyl bromide (PFOB) (17 fluorine atoms), a superfluorinated probe called PERFECTA (bearing 36 chemically equivalent fluorine atoms per molecule) [42], or perfluoropolyethers (PFPE) (with more than 40 fluorine atoms per molecule). These probes possess convenient features for in vivo applications such as nontoxicity, biological and chemical inertness and the ability to be internalized into cells, enabling their labeling. In this way, e.g., macrophages, stem cells, immune cells [8, 11, 13], or even clusters of cells such as pancreatic islets [17, 43] may be visualized and tracked. PFCs are both hydrophobic and lipophobic, and thus, liquid PFC emulsions must be stabilized with surfactants (lipids or phospholipids) or entrapped in polymer nanoparticles [44, 45] for stabilization and biocompatibility [15, 44]. There are many preclinical applications using PFC-based agents covering the imaging of cardiac progenitor stem cells and bone-derived bone marrow macrophages [15], detection of dendritic cells [46], visualization of the immune response [47, 48], tracking of cells or pancreatic islets [43], etc. PFCs with a single ¹⁹F MR peak in their spectra have been implemented in various studies, including a clinical trial with labeled dendritic cells (DCs) intended for adenocarcinoma treatment [12]. Although widely implemented, PFCs also have limitations, such as nonspecific accumulation in tissues or at the site of inflammation [49], possible macrophage activation after high dosage [50], altered cellular responses due to the incorporation of PFCs into the cellular membranes [1] and long retention times in the body.

In addition to cell labeling and tracking, fluorine-containing probes can also be implemented for other purposes. Recently, polymer agents consisting of molecular hydrophobic and hydrophilic blocks (copolymers) have shown promising properties for biomedical applications, especially for tumor diagnosis based upon their responsiveness to the chemical environment or as possible drug carriers due to their nanoscale size. These probes can carry large amounts of fluorine atoms, resulting in a high sensitivity of visualization, although their short relaxation times resulting from polymerization need to be adjusted. In the majority of these amphiphilic agents, the fluorinated block is based on acrylic acid, specifically on 2,2,2-trifluorethylacrylate (TFEA), 2,2,2-trifluorethyl methacrylate (TFEMA), poly[N-(2,2-difluorethyl)acrylamide] (PDFEA) [39, 40] or octafluoropentyl methacrylate (OFPMA). There are also polymers based on functionalized styrenes (e.g., 2,3,4,5,6-pentafluorostyrene (PFS)) [51] or polydimethylsiloxanes (PDMS) [52]. These probes are described in more detail in the section “Polymer agents for drug delivery”

Fluorine-containing agents can also be targeted to specific structures (e.g., the cell surface); accumulated in specific cells such as macrophages, stem cells and immune cells [1, 53]; and responsive to specific stimuli in the environment (physiological processes, enzymatic activity, concentrations of metal ions, pH or pO₂) [3, 35, 54‐56].

Preparation of fluorinated probes

The most commonly employed probes are PFCs, which are typically used as stabilized aqueous (nano)emulsions prepared under high pressure; emulsification is usually performed by probe sonication. An emerging class of ¹⁹F probes are fluorinated polymers. These polymers can be used either alone or as colloidal stabilizers for PFCs. Fluorinated copolymers are typically synthesized analogously to their nonfluorinated counterparts, i.e., by (controlled pseudo living) radical, cationic, anionic or coordination polymerization. The most commonly used controlled radical polymerization techniques involve nitroxide-mediated polymerization [66, 67], atom transfer polymerization (ATRP) [68, 69] and reversible addition fragmentation chain transfer (RAFT) polymerization [70, 71]. It is worth mentioning that if multiple fluorine atoms are in close proximity to the polymerizable moiety, then they may dramatically reduce the electron density of the moiety, greatly influencing its reactivity to polymerization. Other procedures to introduce fluorine atoms into polymer structures involve fluoroalkanoyl peroxide initiation [72, 73], telomerizations with fluorinated mercaptan and fluorinated iodides [74] and esterification with perfluoroacyl chloride [75]. The fluorine block can also be introduced within the termination process [76]. The various copolymer structures include linear copolymers, hyperbranched copolymers, dendrimers [77‐79], micelles [80] and star- and knedel-like structures [51, 65].

Properties of fluorinated polymers

A high density of equivalent fluorine atoms is required in the probes suitable for ¹⁹F MRI. However, (per)fluorinated—fluorophilic parts of the molecules/polymer blocks are naturally insoluble in water and aggregation of ¹⁹F probes with high fluorine content is often observed in aqueous solution. This causes attenuation of MR signal and decreasing the ¹⁹F MR sensitivity. Therefore, it is necessary to solubilize them in aqueous milieus for their use as contrast agents. This may be done by adding covalently bound sufficiently hydrophilic moieties or polymer block(s) or by noncovalent incorporation of fluorophilic molecules into supramolecular assemblies containing amphiphiles solubilizing the whole system in aqueous milieu.

The specific advantage of polymer systems, especially from a diagnostic and therapeutic point of view, is the possibility to construct delivery systems for drugs, nucleic acids, imaging labels or radionuclides to target cancerous tissue, macrophages or other cells and their subcellular compartments. The polymer systems can easily build “molecular toolboxes”, which can be targeted and used as efficient theranostic tools [81]. Self-assembled (supramolecular) polymer systems are very promising. Supramolecular polymer systems are assembled from many molecules that can be bound together by various noncovalent interactions, such as hydrophobic, ion–ion, and coordination interactions [82, 83]. The degradability of such systems may be controlled not only chemically but also physically. According to the type of bonds and molecules, different polymer systems can be created, such as polymer micelles, polymersomes, polyplexes, and polymer nanoparticles [76, 84]. Many fluorinated polymers exhibit self-assembly properties, which are based on the ability of fluorinated molecules to phase separate and assemble into a fluorous phase that is both hydrophobic and lipophobic. The advantage of the self-assembly feature is its dependency on environmental conditions; therefore, these agents can act primary as environmentally responsive probes. These systems are responsive to external stimuli, such as changes in pH, temperature, redox potential, enzymes, and ion concentrations. Their features can be used for custom-built self-assembling scaffolds and depots.

From an imaging point of view, the challenge in synthesizing multiblock copolymers is ensuring high fluorine contents and suitable relaxation times for ¹⁹F MRI. Under optimal conditions, the T₁ relaxation time should not be too long for recovery of the longitudinal magnetization; T₁ relaxation times of many fluorinated molecules are in the range of 1–4 s, which results in long acquisition times for in vivo experiments [85, 86]. Fluorine T₂ relaxation times are based on the mobility of the fluorine segments and need to be adjusted to permit imaging by standard spin, gradient and ultrashort echo time (UTE) sequences [37], which means the T₂ relaxation times should not be too short (> 10 ms). Adjustment of the relaxation times is crucial and challenging, and various chemical approaches have been tested [53, 87‐89]. For instance, control over the molecular mobility can be achieved by preventing the very strong fluorine–fluorine interactions by hydration of the fluorosegments [19]. Moreover, the association of the fluorine segments needs to be taken into account due to strong dipole–dipole interactions and shortening of the relaxation times [63]. The proximity of paramagnetic atoms, such as lanthanides, also highly influences fluorine relaxation.

From a diagnostic point of view, fluorine-containing contrast agents possess the added value of specificity and responsiveness. The specificity can be achieved by modification with a targeting moiety; therefore, it is crucial to prepare easily modifiable chemical structures for the probes.

In summary, a polymer probe suitable for ¹⁹F MRI should possess:

a high content of equivalent fluorine atoms so that all of them fit into the chemical shift window of interest,

efficient mobility and limited association resulting in suitable relaxation times,

adequate solubility in water,

an easily modifiable structure for targeting, and

reliable pharmacokinetic and pharmacodynamic properties, including biodegradability and elimination after the probe fulfills its task

Polymer perfluorocarbons

The commercially available PFC-based probes include the PFPE-based agents Cell Sense and V-Sense (CS-1000-DM-Red and VS-1000H, Celsense, Inc., Pittsburgh, USA). These types of probes were introduced in the 1980s for tumor detection [60, 61], and their use as a cell label was shown for the first time in 2005 [8]. Although PFPE-based agents have been implemented in various preclinical and clinical studies, they are difficult to further functionalize, and the possible extra covalent bond would break the symmetry of the probe, which could lead to multiple ¹⁹F peaks [42]. Therefore, there is a need for the synthesis of novel probes with higher fluorine content and the potential for easy modification. In 2017, Zhang et al. [62] synthesized a polymer agent based on PFPE with a high fluorine content between 10 and 29% wt. The polymer consists of PFPE end-functionalized homopolymers of oligo(ethylene glycol) methyl ether acrylate (poly(OEGA)m-PFPE). These polymers are water-soluble and possess outstanding imaging sensitivity as was shown with in vitro and in vivo experiments. The long T₂ relaxation times (> 80 ms) of these PFPE-based probes are suitable for imaging using common MR sequences, such as a spin-echo-based sequence. The polymers accumulated in the liver, kidneys and spleen of mice after intravenous administration of the probe. The difference in the ratio of hydrophobic (PFPE) and hydrophilic [oligo(ethylene oxide) methyl ether acrylate] segments played an important role in the accumulation of the probe in biological tissue. The polymer showed resistance to rapid uptake by macrophages and thus longer circulation times in the blood. This effect is also seen in other studies [90, 91]. The polymer with exposed PFPE segments showed enhanced recognition and filtration by macrophages, resulting in faster clearance from the body.

Fluorine molecular blocks

Development of fluorine copolymers for ¹⁹F MRI: from chemical concept to first in vivo ¹⁹F MR images

Since the first reports on the synthesis of copolymers consisting of fluorinated molecular blocks, these probes have been extensively studied. In 2007, Cheng et al. [52] introduced a hyperbranched fluorinated copolymer consisting of a fluorinated backbone and PDMS. The proposed cross-linking of the hyperbranched fluoropolymers with PDMS or poly(ethylene oxide) (PEO) showed unique properties, such as an anti-biofouling ability, release behavior for various molecules and mechanical performance [92]. This approach inspired the further synthesis of ¹⁹F copolymers intended for ¹⁹F MRI. In 2008, the Wooley group synthesized polymers of trifluorethyl methacrylates and acrylic acid grafted onto a hydrophobic hyperbranched core. The fluoropolymers possessed good imaging properties (T₁/T₂ = 500/50 ms) and achieved a high SNR in a phantom study, although with an extensive scanning time (13 h) [93]. Later, this group studied the imaging performance of styrene-based polymers and observed that the packaging of fluorine-rich segments into the core restricts the mobility of the chains and limits ¹⁹F detectability [51]. The polymers had to be dissolved in dimethyl sulfoxide (DMSO) to increase their mobility, which increased the sensitivity of ¹⁹F MR signal detection in MR spectra; therefore, this approach is not suitable for biological applications due to the toxicity of DMSO.

The first report of ¹⁹F MRI of fluorinated copolymers was published in 2009 by Peng et al. [64]. This group synthesized diblock copolymers of acrylic acid with partially fluorinated acrylate or methacrylate monomers, which undergo spontaneous assembly in mixed or aqueous solvents resulting in the formation of micelles (diameter 20-45 nm). The micelles exhibited a strong signal in ¹⁹F MR images, with a higher signal obtained from the methacrylate polymers compared to the acrylate polymers due to the short T₂ relaxation times of the acrylate. The ¹⁹F T₁ relaxation times were approximately 500 – 600 ms, and the ¹⁹F T₂ relaxation times were 331 ms and 249 ms for TFEA and TFEMA, respectively. These ranges for the T₁ and T₂ relaxation times are suitable for visualization with routinely used MR imaging sequences without the need to use UTE or zero echo time (ZTE) sequences. The ¹⁹F MR images of phantoms containing the copolymers were acquired within 1 h 20 min using a 3D spin-echo sequence at 7 T (2.5 mm slice thickness). The low ¹⁹F MR signal detection attributed to the restricted mobility of the fluorinated segments; however, the group later introduced various approaches to increase the mobility of the fluorinated segments while maintaining the high amount of ¹⁹F atoms in a molecule. In 2010, the group reported an approach to enhance the hydration of the fluorinated blocks by preventing their aggregation in water by exploiting the electrostatic repulsion between monomeric units, which contributed to higher detectability [94].

Then, in 2010, highly flexible hyperbranched polymers that maintained the molecular mobility of the fluorinated chains were introduced by Thurecht et al. [80]. Moreover, this cytocompatible hyperbranched polymer can be easily functionalized for tracking or targeting. The polymer possesses “shape-resistance”, which is important for cell targeting and ensures the proper orientation for biological recognition. To eliminate the toxic effect of the cationic hyperbranched core, PEO monomethylether methacrylate (PEOMA) was incorporated into the molecule. Importantly, the polymer had been modified with mannose for biological targeting, e.g., the immune responses mediated by macrophages, which possess DC-SIGN surface receptors for mannosylated species. Fluorine T₂ relaxation times of the polymers were in the detectable range (68–122 ms).

The same group reported a study focused on testing the solvent influence on an assembly of TFEA/TFEMA-based polymers [63]. Diffuse aggregates were formed in dichloromethane and micelles were formed in acetone. After the addition of water to these systems, both systems formed cylindrical structures. The highest ¹⁹F MR signal was observed from polymers dissolved in acetone, which highlights the dependence of imaging properties on the solvent used due to the rigidity of the structure. Association of the fluorine segments leads to strong dipole–dipole interactions between the ¹⁹F spins, causing shortening of the ¹⁹F spin–spin relaxation times and therefore lowering the ¹⁹F MR detectability. To overcome the effect of dipole–dipole interactions, several approaches for improving MRI detectability were proposed, such as distributing the monomers along the polymer chain, incorporating branches and limiting the content of the fluorinated monomers [63]. Although this study was performed in biologically irrelevant organic solvents, it reveals rules of general applicability.

Fluorine copolymers responsive to environmental changes: from optimization of the chemical structure to biological applications

In addition to the use of fluorine copolymers for contrast modulation in ¹⁹F MR images, various probes also respond to environmental stimuli and can act as responsive probes for, e.g., controlled in situ supramolecular nanostructure formation due to external environment change or even responsive ¹⁹F MRI. The rationale for such a responsive agent would be, e.g., the evaluation of treatment response by changes in pH, controlled release of drugs upon changes in pH, and accumulation of the system at the target site according to pH (acidity in tumors).

The agents mostly respond to changes in pH or temperature by triggering self-assembly. For the synthesis and application of these types of polymers, it is crucial to achieve a lower critical solution temperature (LCST) within an adequate range. The LCST refers to the temperature below which the components of the polymer are miscible. At temperatures above the LCST, polymers lose their hydration layer, start to precipitate and change into a solid phase. As a macroscopic measure, the value most often used is the cloud point temperature (CPT), which is where the polymer visibly phase-separates at the given concentration, where LCST is the temperature minimum in the function CPT = f(concentration). As the components become less mobile, the relaxation times are shortened. These aggregation properties can be implemented in the creation of solid implants without the need for surgical intervention [40, 95].

In 2007, the group of Mao et al. [65] presented amphiphilic hyperbranched star-block copolymers containing poly[2-(N,N-dimethylamino)ethyl methacrylate] (PDMAEMA) and OFPMA, which self-assemble into micelles in either an acidic aqueous solution or in a dimethylformamide/water mixture (both at pH 3). The size (expressed as hydrodynamic diameter, D_H) of the micelles depends on the length of the DMAEMA segment and varies with pH. The authors reported various sizes (50–200 nm) and structures for the synthesized probes ranging from micelles to fibers depending on the length of the protonated PDMAEMA chains. Fluorine MR spectra showed multiple ¹⁹F peaks for the polymer.

Similar thermo- and pH-responsive fluoroalkyl end-capped amphiphilic diblock copolymers containing PDMAEMA and poly[2-(N,N-diethylamino)ethyl methacrylate] (PDEA) were synthesized by the Zhang [96]. These polymers can form flower-like micelles in aqueous solution upon pH changes or by changing the linking order of the PDMA and PDEA blocks. The LCST of these polymers decreases with increasing concentration or pH. At a low pH of approximately 3, there is no aggregation, and the copolymers exist in the aqueous solution as unimers. At a higher pH (7- 9), the copolymer forms micelles, and at a pH of approximately 9, the immiscible components aggregate into a core. By changing the linking order of the PDMA and PDEA blocks and changing the pH, different morphologies were obtained such as sphere-on-sphere, flower-like micelles and anomalous vesicles. Fluorine MR spectroscopy showed three ¹⁹F peaks in the spectra of the polymers.

In another study, PEO-coated nanogels constructed from PEO chains and a polyamine gel core compound with ¹⁹F showed suitable properties for targeting solid tumors via their responsiveness to the low pH (6.5) present in the tumor environment [20]. The polymer prepared from 2-(N,N-diethylamino)ethyl methacrylate (DEAMA) and TFEMA at various molar ratios with PEO chains showed volume phase transition points in the pH range of 6.8–7.3. This effect is caused by the hydrophobicity of the gel core and deprotonization of the amino groups, leading to a broadening of the ¹⁹F MR signals due to the limited molecular motion, suggesting that the PEO-coated nanogels will swell only in the acidic environment of, e.g., tumors (pH 6.5–7.0). This effect was confirmed by ¹⁹F MR spectroscopy; the polymers were only detected at acidic pH, and there was almost no ¹⁹F MR signal in the physiological pH range (7.4). A stable on–off behavior was observed even in the presence of 90% fetal bovine serum, which is promising for future biological applications. The probe showed high sensitivity (the detection threshold as measured by ¹⁹F MR spectroscopy was 55 µM at 12 T), although ¹⁹F MR imaging was not performed in this study.

Polymer agents for drug delivery

In theranostics (therapy + diagnosis), nanoparticles and micelles (with D_H, below 200 nm) can be used for passive targeting of solid tumors due to the enhanced permeability and retention effect (EPR) [97‐99], which is caused by the leaky vasculature and limited lymphatic drainage of solid tumor tissue. Moreover, the probes can be further functionalized to prolong their circulation times [e.g., with PEO or poly(2-methyl-2-oxazolines)] and thus increase their probability of accumulation in tumor tissue [100‐103].

The first example of ¹⁹F MR imaging of the accumulation of fluoropolymers in tumors was reported in 2014 by Rolfe et al. 2014 [19]. In this study, a tunable polymer probe, which targeted melanoma cells and enabled multimodal imaging due to the addition of a fluorescent dye, was introduced. The probe was further functionalized for tumor targeting via modification with folate. The probe was found to be taken up by B16 melanoma cells, which overexpress folate receptors. The probe was detected in the tumors of mice after intravenous administration. Fluorescence and ¹⁹F MR images revealed the accumulation of the probe in the major organs (the liver, kidneys and bladder) 4 h following injection. ¹⁹F MR images of the mice were acquired within 18 min at 16.4 T.

In 2017, the nanoparticles of block copolymers containing a PEO hydrophilic block and a fluorine-containing polymethacrylate block were synthesized by Fu et al. [104]. These polymer nanoparticles exhibit a higher ¹⁹F MR signal in the presence of H₂O₂ (i.e., after micelle disassembly due to hydrophilization after oxidation of the thioethers to sulfoxide), suggesting a promising direction for future biological applications. The sensitivity of the imaging agents was further enhanced by adding a pH switch, resulting in a reactive oxygen species (ROS)/pH dual-responsive ¹⁹F MRI agent. The most pronounced change in the intensity of the ¹⁹F MR signal was achieved in response to the presence of ROS in a mildly acidic environment.

Self-assembled biocompatible polymer nanogels consisting of hydrophilic-thermoresponsive diblock copolymers containing either poly[N-(2-hydroxypropyl)methacrylamide] (PHPMA) or poly(2-methyl-2-oxazoline) (PMeOx) as the hydrophilic block and PDFEA as the fluorinated thermoresponsive block exhibited thermal responsivity, being molecularly soluble at room temperature and forming well-defined nanogels at body temperature (Fig. 1) [39]. The probes exhibit suitable relaxation times (T₁ ≈ 275–312 ms, T₂ ≈ 17–305 ms; at 4.7 T, 37 °C) for visualization by ¹⁹F MRI using standard spin-echo sequences. The presence of both polymers (PMeOx-PDFEA and PHPMA-PDFEA) was observed by ¹⁹F MRI after injection either into the muscle of mice or subcutaneously (Fig. 2). These probes have promising properties for cell tracking or tumor theranostics due to their easily modifiable structure, for incorporation of cell targeting moieties, and their nanosize (approximately 100 nm), allowing passive accumulation in the tumor tissue via the EPR effect.

Fluorinated thermoresponsive polymers can also be implemented for sustained release of drugs from implants, which are created upon injection into the body [105]. Typically, the polymers are injected in an aqueous solution, and after heating to body temperature, which is above the CPT, they form a depot [95, 106]. Above the LCST, the polymers precipitate, and after phase separation, they create a solid depot without surgery [95]. Moreover, if the polymers contain ¹⁹F atoms, the localization, size and biodegradation of the implants can be monitored by ¹⁹F MRI with high sensitivity due to the high local ¹⁹F concentration at the injection site. In our recent study [40], we used a thermoresponsive fluorinated PDFEA copolymer modified with pH-responsive imidazole units, where the pH change from slightly acidic in the injected solution to neutral in the tissue adjusts CPT, allowing for in situ depot formation due to temperature change without the risk of needle obstruction during injection. This multistimuli-responsive agent was tracked by ¹⁹F MRI after intramuscular and subcutaneous administration in rats (Fig. 3). The depot was visualized for 11 months with high sensitivity, indicating that these thermoresponsive polymers can be utilized as injectable solid implants with the possibility of drug incorporation. Importantly, the degradability of the polymers can be tailored in future theranostic applications.

Conclusion and future perspectives

¹⁹F MRI using fluorine-containing agents represents a specific imaging method with applications in both experimental and clinical medicine due to the negligible ¹⁹F MR signals from the body. To achieve sufficient sensitivity of ¹⁹F MRI, novel fluorine-containing probes are needed. Polymer-based probes are a very promising and versatile platform with properties tailorable to a plethora of in vivo biomedical applications. In particular, stimuli-responsive supramolecular polymer nanostructures allowing for functional imaging in response to changes in temperature, pH, reactive oxygen species and other physiological stimuli hold promise for noninvasive functional diagnostics of pathological tissues in the future. Targeted cell labeling for long-term tracking of transplanted cells by ¹⁹F MRI is another highly promising direction for such ¹⁹F agents.

To employ the ¹⁹F MRI polymer probes in practice, especially in clinics, several properties of these probes must be fulfilled. Among them are a high content of fluorine atoms that are chemically equivalent so that all of them fit into the chemical shift window of interest, an efficient mobility and limited association of the fluorine segments resulting in suitable relaxation times, an adequate solubility in water, an easily modifiable structure for targeting, reliable pharmacokinetic/pharmacodynamic properties including biodegradability, clearance of the probe after the system fulfills its task, and the capability of functional imaging if needed in the particular application. Another important challenge that must be solved is the biodegradability of the imaging agents so that the system may be fully eliminated from the organism after fulfilling its task.

Acknowledgements

The authors thank the Czech Science Foundation for financial support (D.J., A.G., M.H.: Grant # 16-03156S and K.K., D.B.: Grant # 18-07983S) and by the Ministry of Health of the Czech Republic (D.J., A.G.: CZ-DRO, IN 00023001).

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Titel: Fluorine polymer probes for magnetic resonance imaging: quo vadis?
verfasst von: Daniel Jirak
Andrea Galisova
Kristyna Kolouchova
David Babuka
Martin Hruby
Publikationsdatum: 29.11.2018
Verlag: Springer International Publishing
Erschienen in: Magnetic Resonance Materials in Physics, Biology and Medicine / Ausgabe 1/2019
Print ISSN: 0968-5243
Elektronische ISSN: 1352-8661
DOI: https://doi.org/10.1007/s10334-018-0724-6

Neu im Fachgebiet Radiologie

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Springer Medizin

Fluorine polymer probes for magnetic resonance imaging: quo vadis?

Abstract

Introduction

Types of fluorine-containing probes

Preparation of fluorinated probes

Properties of fluorinated polymers

Polymer perfluorocarbons

Fluorine molecular blocks

Development of fluorine copolymers for ¹⁹F MRI: from chemical concept to first in vivo ¹⁹F MR images

Fluorine copolymers responsive to environmental changes: from optimization of the chemical structure to biological applications

Polymer agents for drug delivery

Conclusion and future perspectives

Acknowledgements

Compliance with ethical standards

Conflict of interest

Unsere Produktempfehlungen

e.Med Interdisziplinär

e.Med Radiologie

Neu im Fachgebiet Radiologie

Fünf Dinge, die im Kindernotfall besser zu unterlassen sind

„Nur wer sich gut aufgehoben fühlt, kann auch für Patientensicherheit sorgen“

Wie toxische Männlichkeit der Gesundheit von Männern schadet

Studie bestätigt Potenzial von KI in der Radiologie

Update Radiologie

Springer Medizin

Abstract

Introduction

Types of fluorine-containing probes

Preparation of fluorinated probes

Properties of fluorinated polymers

Polymer perfluorocarbons

Fluorine molecular blocks

Development of fluorine copolymers for 19F MRI: from chemical concept to first in vivo 19F MR images

Fluorine copolymers responsive to environmental changes: from optimization of the chemical structure to biological applications

Polymer agents for drug delivery

Conclusion and future perspectives

Acknowledgements

Compliance with ethical standards

Conflict of interest

Unsere Produktempfehlungen

e.Med Interdisziplinär

e.Med Radiologie

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