Patent Application
20170196997
The present invention relates to a rare earth-based nanoparticle magnetic resonance contrast agent and a preparation method thereof, and belongs to the technical field of nano materials.
Magnetic Resonance Imaging (MRI) is an important technique in the medical diagnosis and molecular imaging field, and has such advantages as high tissue resolution, multiple imaging parameters and no radiation damage to human bodies. However, as the MRI technology has a low sensitivity, contrast agents are often employed to improve the imaging contrast ratio and the image quality clinically. According to the ratio of the transverse relaxivity to the longitudinal relaxivity, contrast agents can be divided into two categories: T1 contrast agents brightening local tissues and T2 contrast agents darkening local tissues. With unfilled 4f electronic shells, rare earth ions possess unique optical, electrical and magnetic properties, and thus have important application value in both aspects of magnetic resonance T1 and T2 contrast agents.
In the aspect of T1 contrast agents, trivalent gadolinium ions (Gd3+) have the largest number of unpaired electrons, and a long electron spin relaxation time, which can effectively shorten the longitudinal relaxation time to increase the image lightness, and are thus regarded as the best choice of the T1 contrast agents. In order to reduce the toxicity risk that the free gadolinium ions bring about, currently mostly widely-used T1 contrast agents are gadolinium-containing paramagnetic chelates, to reduce the leakage possibility by a chelating mode. However, such contrast agents typically have a low relaxivity, limited contrasting effect, and a large required dose, and still have potential threats for normal tissues. In addition, as such contrast agents belong to a small molecule and have a short in vivo residence time, the diagnostic effect over a long time cannot be guaranteed.
In the aspect of T2 contrast agents, superparamagnetic iron oxide nanoparticles as contrast agents have been commercialized, but unfortunately such contrast agents will reach a saturated magnetization at a relatively low magnetic field strength (1.5 T), and therefore the contrasting effect is poor at a higher magnetic field strength (NaDyF4 Nanoparticles as T-2 Contrast Agents for Ultrahigh Field Magnetic Resonance Imaging, Frank C. J. M. van Veggel, et al. J. Phys. Chem. Lett. 2012, 3, 524-529). However the rare earth ions (such as terbium Tb3+, dysprosium Dy3+, holmium Ho3+, erbium Er3+) have a large magnetic moment and a short electron spin relaxation time; therefore, they are expected to meet the requirements of contrasting at a high magnetic field strength.
In summary, rare earth-based nanoparticles are expected to become a new generation of highly efficient magnetic resonance contrast agents, because individual particles contain a large amount of rare earth ions, and can produce a more significant signal enhancement, and the rigid skeleton of inorganic nano structures can reduce the leakage possibility of the rare earth ions. Moreover, as the sizes of nanoparticles are greater than those of chelates, the in vivo circulation time is relatively long. In addition, the surfaces of inorganic nano structures can be easily modified with functional groups to achieve the purposes of active targeting, and multi-mode imaging and so on. Therefore, the development and utilization of the rare earth-based nanoparticle magnetic resonance contrast agent has a considerable significance for improving diagnostic accuracy and safety of the contrast agent.
The present invention provides a rare earth-based nanoparticle magnetic resonance contrast agent and a preparation method thereof, and the magnetic resonance contrast agent has such advantages as high relaxivity, small injection dose, long in vivo circulation time, and low leakage possibility of the rare earth ions.
The rare earth-based nanoparticle magnetic resonance contrast agent of the present invention refers to rare earth-based inorganic nanoparticles with the surfaces thereof coated with hydrophilic ligands. In the present invention, the rare earth-based nanoparticles are first obtained by a high-temperature oil phase reaction, and then the surfaces thereof are coated with hydrophilic molecules to obtain the rare earth-based nanoparticle magnetic resonance contrast agent.
Rare earth elements (RE) in the rare earth-based nanoparticle magnetic resonance contrast agent of the present invention comprise one or more of lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), lutetium (Lu), scandium (Sc), and yttrium (Y).
The composition of the rare earth-based nanoparticles in the rare earth-based nanoparticle magnetic resonance contrast agent of the present invention is MaREObXC, wherein RE represents a rare earth element, M represents an alkali or alkaline earth metal, X represents a fluorine or chlorine, 0≦a≦1, 0≦b≦1.5, and 0≦c≦4. In addition, the rare earth-based nanoparticles can also be an inorganic compound doped by using MaREObXc as a substrate, and the doping serves to impart them a luminescent property or control their magnetic property.
The surface coating ligands of the rare earth-based nanoparticle magnetic resonance contrast agent of the present invention can employ one or more of the following: a small hydrophilic molecule such as citric acid and cysteine, and a hydrophilic polymer such as a polyvinyl alcohol, polyethyleneimine, polyvinyl pyrrolidone, and polyacrylic acid.
The present invention provides a preparation method of a rare earth-based nanoparticle magnetic resonance contrast agent, wherein the method comprises the following steps:
1) adding a certain amount of a rare earth precursor or a mixture of a rare earth precursor and a non-rare earth precursor into a high-boiling organic solvent to obtain a solution A;
2) performing vacuum pumping on the solution A to remove moisture, then heating up to 250-340° C. under the protection of an inert gas and maintaining for 15 min-24 h, and then cooling to room temperature to obtain a sol B;
3) performing centrifugal separation on the sol B, washing the obtained precipitate, and then coating the surface of the precipitate with hydrophilic ligands;
4) dispersing the coated particles into a solvent to obtain the contrast agent.
In step 1), the molar ratio of the precursor to the solvent is preferably 1:20-1:200, the rare earth precursor in the precursor must be added, and whether the non-rare earth precursor needs to be added depends on the composition of a target product; in step 2), vacuum pumping is performed preferably at 100-140° C.; in step 3), a large amount of ethanol is preferably employed to wash, a washing manner is preferably centrifugal washing, and washing is preferred for 2 to 6 times; and in step 4), the solvent is preferably water or physiological saline.
The high-boiling organic solvent in the present invention refers to a mixed solvent composed of one or more of oleic acid, linoleic acid, oleylamine, octadecene, hexadecylamine and octadecylamine.
The rare earth precursor in the present invention is a mixture of one or more of the following: rare-earth hydroxides, oxalates, acetates, trifluoroacetates, trichloroacetates, acetylacetonates, and phenyl acetylacetonates.
The non-rare earth precursor in the present invention is a mixture of one or more of the following: alkali-metal and alkaline earth-metal fluorides, hydroxides, oxalates, acetates, trifluoroacetates, trichloroacetates, acetylacetonates, and phenyl acetylacetonates.
In the preparation method of the rare earth-based nanoparticle magnetic resonance contrast agent of the present invention, the composition, size, shape and crystallization of the rare earth-based nanoparticles can be adjusted by adjusting the parameters of the solvent ratio, the feeding amount of the precursor, the reaction temperature, the reaction time, and the like; and the relaxation property, the biocompatibility and the like of the contrast agent can be adjusted by the parameters of the type, the feeding amount and the like of water-soluble molecules during the surface coating of the hydrophilic ligands.
The rare earth-based nanoparticle magnetic resonance contrast agent of the present invention has the following advantages:
1. the individual particles of the magnetic resonance contrast agent of the present invention contain a large number of rare earth ions, which can significantly reduce the relaxation time of surrounding protons;
2. the magnetic resonance contrast agent of the present invention has a larger size than chelates, and a long in vivo circulation time, which can meet the requirement of a long time clinical diagnosis;
3. the magnetic resonance contrast agent of the present invention has a relatively high relaxivity, which can be about ten times higher than that of the clinically commonly-used contrast agent, and therefore provides a better contrasting effect under the condition of the same concentration;
4. the magnetic resonance contrast agent of the present invention has a rigid skeleton of an inorganic nano structure, which can reduce the leakage possibility of rare earth ions, and therefore is safer compared with chelates;
5. since the magnetic resonance contrast agent of the present invention features an excellent imaging performance, the required dose can be greatly reduced compared with the currently clinically commonly-used contrast agent, further reducing the safety risk;
6. the magnetic resonance contrast agent of the present invention features easy control, simple reaction operations, good repeatability, and stable properties.
The following describes the rare earth-based nanoparticle magnetic resonance contrast agent and the preparation method thereof of the present invention in connection with specific embodiments, so as to make the public better understand the technical contents, rather than to limit the technical contents. Actually, the improvements which are made for the composite material and the preparation method thereof with same or similar principles all fall within the protection scope of the present application. The following only takes a 50 ml capacity reaction system as an example to exemplify the embodiments, and the present invention can be implemented in a mode of same proportional amplification of each material in actual preparations.
Synthesis of Gd2O3 nanoparticles: adding 0.5 mmol of gadolinium acetylacetonate into a mixed solvent of oleic acid (4 mL) and oleylamine (12 mL), heating up to 340° C. under the protection of an inert gas, maintaining the temperature for 15 min, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the Gd2O3 nanoparticles.
Synthesis of Pr2O3 nanoparticles: adding 0.5 mmol of praseodymium acetate into a mixed solvent of oleic acid (6 mL) and oleylamine (12 mL), heating up to 340° C. under the protection of an inert gas, maintaining the temperature for 2 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the Pr2O3 nanoparticles.
Synthesis of Er2O3 nanoparticles: adding 0.5 mmol of phenyl erbium acetylacetonate into a mixed solvent of oleic acid (6 mL) and oleylamine (8 mL), heating up to 310° C. under the protection of an inert gas, maintaining the temperature for 1 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the Er2O3 nanoparticles.
Synthesis of Y2O3 nanoparticles: adding 0.5 mmol of yttrium hydroxide into a mixed solvent of oleic acid (2 mL), oleylamine (3 mL), and octadecene (5 mL), heating up to 310° C. under the protection of an inert gas, maintaining the temperature for 1 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the Y2O3 nanoparticles.
Synthesis of LaF3 nanoparticles: adding 1 mmol of lanthanum trifluoroacetate and 0.5 mmol of lithium fluoride into a mixed solvent of oleic acid (20 mmol) and octadecene (20 mmol), heating up to 260° C. under the protection of an inert gas, maintaining the temperature for 4 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the LaF3 nanoparticles.
Synthesis of CeOF nanoparticles: adding 1 mmol of cerium oxalate into a mixed solvent of oleic acid (5 mmol) and hexadecylamine (35 mmol), heating up to 320° C. under the protection of an inert gas, maintaining the temperature for 1 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the CeOF nanoparticles.
Synthesis of EuOCl nanoparticles: adding 1 mmol of europium trichloroacetate into a mixed solvent of oleic acid (20 mmol) and octadecene (20 mmol), heating up to 330° C. under the protection of an inert gas, maintaining the temperature for 1 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing twice to obtain the EuOCl nanoparticles.
Synthesis of NaDyF4:Yb,Er nanoparticles: adding 0.78 mmol of dysprosium trifluoroacetate, 0.20 mmol of yttrium trifluoroacetate, 0.02 mmol of erbium trifluoroacetate, and 1 mmol of sodium trifluoroacetate into a mixed solvent of oleic acid (10 mmol), octadecylamine (10 mmol), and octadecene (20 mmol), heating up to 250° C. under the protection of an inert gas, maintaining the temperature for 0.5 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing four times to obtain the NaDyF4:Yb,Er nanoparticles.
Synthesis of LiTmF4 nanoparticles: adding 1 mmol of lithium trifluoroacetate and 1 mmol of thulium trifluoroacetate into a mixed solvent of oleic acid (20 mmol) and octadecene (20 mmol), heating up to 320° C. under the protection of an inert gas, maintaining the temperature for 15 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing six times to obtain the LiTmF4 nanoparticles.
Synthesis of KYb2F7 nanoparticles: adding 1 mmol of potassium trifluoroacetate and 1 mmol of ytterbium trifluoroacetate into a mixed solvent of oleic acid (20 mmol) and octadecene (20 mmol), heating up to 310° C. under the protection of an inert gas, maintaining the temperature for 2 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing six times to obtain the KYb2F7 nanoparticles.
Synthesis of BaYF5 nanoparticles: adding 1 mmol of barium oxalate and 1 mmol of yttrium trifluoroacetate into a mixed solvent of linoleic acid (10 mmol), oleic acid (10 mmol) and octadecylamine (20 mmol), heating up to 340° C. under the protection of an inert gas, maintaining the temperature for 24 h, cooling the reaction solution to room temperature, adding a large amount of ethanol thereinto, and performing centrifugal washing six times to obtain the BaYF5 nanoparticles.
Coating citric acid on particle surfaces: dispersing Gd2O3 nanoparticles (0.1 mmol) obtained in Embodiment 1 into 5 ml of chloroform, adding a citric acid aqueous solution (n/n=20), and vigorously stirring at room temperature for at least 6 h; taking the upper suspension liquid, adding a large amount of ethanol and centrifuging, and dispersing the obtained precipitate into pure water to obtain the nanoparticle magnetic resonance contrast agent.
Coating cysteine on particle surfaces: dispersing Y2O3 nanoparticles (0.1 mmol) obtained in Embodiment 4 into 5 ml of chloroform, adding a cysteine aqueous solution (n/n=30), and vigorously stirring at room temperature for at least 6 h; taking the upper layer suspension liquid, adding a large amount of ethanol and centrifuging, and dispersing the obtained precipitate into pure water to obtain the nanoparticle magnetic resonance contrast agent.
Coating polyvinyl alcohol on particle surfaces: dispersing CeOF nanoparticles (0.1 mmol) obtained in Embodiment 6 into 10 ml of cyclohexane, adding 10 mL of N,N-dimethyl formamide and 50 mg of nitrosonium tetrafluoroborate, and vigorously stirring at room temperature for no less than 1 h; taking the lower layer liquid, adding a large amount of toluene and centrifuging, dissolving the obtained precipitate into 10 mL of N,N-dimethyl formamide again, adding 50 mg of polyvinyl alcohol, and stirring for no less than 4 h; then adding a large amount of acetone into the solution, centrifuging, and dispersing the obtained precipitate into pure water to obtain the nanoparticle magnetic resonance contrast agent.
Coating polyethylene imine on particle surfaces: dispersing LaF3 nanoparticles (0.2 mmol) obtained in Embodiment 5 into 10 ml of cyclohexane, adding 10 mL of N,N-dimethyl formamide and 50 mg of nitrosonium tetrafluoroborate, and vigorously stirring for no less than 1 h; taking the lower layer liquid, adding a large amount of toluene and centrifuging, dissolving the obtained precipitate into 10 mL of N,N-dimethyl formamide again, adding 50 mg of polyethylene imine, and stirring for no less than 4 h; then adding a large amount of acetone into the solution, centrifuging, and dispersing the obtained precipitate into pure water to obtain the nanoparticle magnetic resonance contrast agent.
Coating polyethylene pyrrolidinone on particle surfaces: dispersing NaDyF4:Yb,Er nanoparticles (0.2 mmol) obtained in Embodiment 8 into 10 ml of cyclohexane, adding 10 mL of N,N-dimethyl formamide and 50 mg of nitrosonium tetrafluoroborate, and vigorously stirring for no less than 1 h; taking the lower layer liquid, adding a large amount of toluene and centrifuging, dissolving the obtained precipitate into 10 mL of N,N-dimethyl formamide again, adding 50 mg of polyethylene pyrrolidinone, and stirring for no less than 4 h; then adding a large amount of acetone into the solution, centrifuging, and dispersing the obtained precipitate into pure water to obtain the nanoparticle magnetic resonance contrast agent.
The rare earth-based nanoparticle magnetic resonance contrast agent of the present invention can significantly reduce the relaxation time of surrounding protons, thereby greatly increasing the contrast ratio of local tissues. The rare earth-based nanoparticle magnetic resonance contrast agent of the present application has such advantages as high relaxivity, long in vivo residence time, low injection dose, and small leakage possibility of the rare earth ions and the like, and can effectively increase the diagnostic accuracy and the safety of the contrast agent.
The foregoing described embodiments of the present invention are not intended to limit the present invention. Those skilled in the art can make some changes and modifications without departing from the spirit and scope of the invention. Therefore the protective scope of the present invention is defined only by the claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201410233943.9 | May 2015 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2014/079597 | 6/10/2014 | WO | 00 |
