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Preparation of supramolecular dendritic nano aggregate for magnetic resonance imaging contrast

A magnetic resonance imaging and supramolecular technology, applied in preparations for in vivo tests, emulsion delivery, pharmaceutical formulations, etc., can solve the problems of long detection time, expensive detection costs, low sensitivity, etc., and achieve simple preparation methods and enhanced Effect of relaxivity, strong bonding ability

Inactive Publication Date: 2013-09-18
NANKAI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the disadvantages of magnetic resonance imaging detection are low sensitivity, long detection time and high detection cost. Therefore, it is necessary to use magnetic resonance contrast agents to enhance and expand the application of magnetic resonance imaging in the field of molecular imaging. See: E. Terreno, D. D. Castelli, A. Viale, S. Aime. Chem. Rev. 2010,110, 3019?3042

Method used

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  • Preparation of supramolecular dendritic nano aggregate for magnetic resonance imaging contrast
  • Preparation of supramolecular dendritic nano aggregate for magnetic resonance imaging contrast
  • Preparation of supramolecular dendritic nano aggregate for magnetic resonance imaging contrast

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Embodiment

[0023] A method for preparing a supramolecular dendritic nano-aggregate for magnetic resonance imaging contrast, comprising the steps of:

[0024] 1) Dissolve 874.0mg of 6-isothiocyanato-6-deoxy-permethylated β-cyclodextrin and 29mg of tris(2-aminoethyl) in 10mL of acetonitrile solvent under the protection of argon, at 25℃ The mixture was stirred at high temperature for 10 hours, the solvent was removed by rotary evaporation, and the remaining solid was purified by column chromatography to obtain 500 mg of white trisPMCD solid with a yield of 60%.

[0025] 1 H NMR (400 MHz, CDCl 3 , δ): 7.27 (s, 3H), 6.28 (s, 3H), 5.24 – 5.07 (m, 15H), 5.04 (s, 3H), 4.97 (s, 3H), 4.12 – 3.26 (m, 291H), 3.19 (dd, J = 9.6, 3.3 Hz, 21H), 2.80 (6, 3H). 13 C NMR (100 MHz, CDCl 3 , δ): 182.6, 99.6, 98.8, 82.0, 81.7, 81.1, 80.1, 71.2, 70.9, 70.9, 61.3, 59.0, 58.6, 58.4, 53.0, 43.5. HRMS (MALDI, m / z ): [ M + Na] + calcd for C 195 h 345 o 102 N 7 S 3 Na + 4536.1079; found, 4536.1451. ...

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Abstract

The invention provides preparation of supramolecular dendritic nano aggregate for magnetic resonance imaging contrast. A construction unit utilizes bridged trimer full-methylated beta-cyclodextrin as a subject and utilizes manganese porphyrin as an object, and a supramolecular assembly is constructed through subject-object inclusion complexation interaction. The preparation method comprises the following steps: 1) dissolving 6-isothiocyano-6-deoxy-fully methylated beta-cyclodextrin and tri(2-aminoethyl) in acetonitrile under argon protection, stirring the solution at room temperature overnight, removing the solvent by rotary evaporating, purifying the residual solid through column chromatography to obtain faint yellow solid; and 2) dissolving the solid and manganese porphyrin in water, and uniformly mixing the ingredients, and adding sodium ascorbate to prepare the target object. The preparation method provided by the invention has the advantages that the ingredients of the supramolecular dendritic nano aggregate have strong bonding ability and can effectively improve the water relaxation ability, thereby having a broad application prospect in the field of magnetic resonance imaging contrast agents; and the preparation method is simple and is beneficial to realizing large-scale popularization and application.

Description

technical field [0001] The invention belongs to nano supramolecular materials, in particular to the preparation of supramolecular dendritic nano aggregates for magnetic resonance imaging contrast. Background technique [0002] Magnetic Resonance Imaging (Magnetic Resonance Imaging) is a new type of high-tech imaging examination method in recent years, which uses non-invasive radiation to obtain spatially and temporally resolved three-dimensional (3D) images of the entire living body. Although this new diagnostic technique was only used in clinical medicine in the early 1980s, it has no ionizing radiation (radiation) damage, no bony artifacts, and can be multi-directional (transverse, coronal, sagittal, etc.) With unique advantages such as multi-parameter imaging, high soft tissue resolution, and the ability to display vascular structures without the use of contrast agents, it has become the main means of diagnosis and monitoring of some diseases, see: 1) C. H. Polman, S. C....

Claims

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Application Information

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IPC IPC(8): A61K49/18A61K49/12
Inventor 刘育孙默张衡益胡心悦刘博闻
Owner NANKAI UNIV
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