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Preparation method and application of paas@mno(oh)-rgd drug release carrier

A carrier and drug technology, applied in the field of PAAs@MnO-RGD drug release carrier, can solve the problems of high valence, small r1 value of contrast agent, and difficulty in forming complexes, and achieves a simple preparation process, easy degradation, and reduced usage. Effect

Inactive Publication Date: 2018-07-17
FUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, Mn is not easy to form complexes, and the price changes more, so the r1 value of contrast agents developed based on manganese oxides is small (generally 0.5 mM -1 ·S -1 )

Method used

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  • Preparation method and application of paas@mno(oh)-rgd drug release carrier
  • Preparation method and application of paas@mno(oh)-rgd drug release carrier
  • Preparation method and application of paas@mno(oh)-rgd drug release carrier

Examples

Experimental program
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Effect test

Embodiment 1

[0033]The aqueous solution of PAAs@MnO(OH) composite nanospheres was ultrasonically treated for 0.5 h, then dropped on the copper grid, dried and then scanned by TEM (see Figure 1(A), Figure 1(B)). The results are shown in Figure 1(A ), as shown in Figure 1(B), it can be seen from Figure 1(A) that the PAAs@MnO(OH) composite nanomaterial is a nanosphere structure with uniform size and an average diameter of about 80 nm; from Figure 1(B) It can be known that the diameter of the MnO(OH) nanoparticles wrapped on the surface of PAAs is about 2 nm, and the size is uniform and the distribution is uniform (pointed by the arrow). From the XRD test results, it can be seen that what is wrapped on the product PAAs is manganese oxyhydroxide nanoparticles (see figure 2 ).

Embodiment 2

[0035] The PAAs@MnO(OH) complex and doxorubicin (DOX) were added to the PBS (10 mM, pH=7.4) solution at a mass concentration of 1:1, shaken at room temperature for 12 h in the dark, centrifuged, and washed with PBS (10 mM , pH=7.4) solution was washed, the supernatant was collected, the amount of DOX contained in it was calculated according to the standard curve of DOX, and the loading amount of DOX was further calculated as 0.911 mg DOX / 1mgPAAs@MnO(OH). Disperse 1 mg of the PAAs@MnO(OH) complex after adsorbing the drug in 3 ml of PBS (10 mM, pH=7.4) solution, put it into a dialysis bag, add the dialysis bag to 47 ml of PBS solution for dialysis for 48 h, and 1 hour, 2 hours, 4 hours, 6 hours, 8 hours, 10 hours, 12 hours, 14 hours, 16 hours, 24 hours, 36 hours, and 48 hours, take 3 ml of the solution to measure the fluorescence, and add 3 ml of PBS to the original solution solution, the test results are as follows image 3 Shown: Curve 1 is normal temperature, pH=7.4; Curve 2...

Embodiment 3

[0037] HepG2 cells were used as target cancer cells to examine the cell biocompatibility of PAAs@MnO(OH) nanomaterials: the liver cancer HepG2 cells were seeded in a 96-well plate, the culture medium required by the cells was added, and then cultured in a cell incubator for 24 After 1 h, the culture solution was taken out, and the PAAs@MnO(OH) nanomaterial prepared in Example 1 was added at concentrations of 5 μg / ml, 15 μg / ml, 25 μg / ml, 50 μg / ml and 100 μg / ml ml of PAAs@MnO(OH) complex to carry out the MTT test, four parallel groups for each concentration, after incubation for 24 h, then read the absorbance value at 490 nm on a microplate reader, according to the absorbance of the blank group and the sample group Calculate the survival rate of cells in each group. From Figure 4 It can be seen from the results that the survival rate of cells in each group is above 90%, indicating that PAAs@MnO(OH) nanospheres have good biocompatibility and no obvious toxicity, even at high co...

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Abstract

The invention provides a preparation method and application of a PAAs@MnO(OH)-RGD drug release carrier.The preparation method comprises the steps of firstly, assembling a manganese oxide hydroxide shell layer on the surface of a sodium polyacrylate nanosphere, so that a composite nanosphere is obtained; making the composite nanosphere be subjected to electrostatic adsorption action, and adsorbing RGD polypeptide molecules to the surface of the composite nanosphere, so that the drug release carrier is obtained.The drug release carrier prepared through the method has the characteristics of tumor location pH and reducing agent dual-response magnetic resonance imaging and drug controlled release and meanwhile has the advantages of being high in drug load rate, biodegradable and the like, and therapy integrating nuclear magnetic imaging, drug delivery and release and targeting on tumors or inflammatory tissues can be achieved.

Description

technical field [0001] The invention belongs to the field of nanomaterial preparation, in particular to a PAAs@MnO(OH)-RGD drug release carrier and its application. Background technique [0002] Tumor is a common and frequently-occurring disease, among which malignant tumor is the most serious disease that endangers human health. According to the latest disease data in my country, in the latest "2015 China Tumor Registration Annual Report", every minute, 6 people across the country are diagnosed with malignant tumors, and 5 people die of cancer. Therefore, with the increasing morbidity and mortality of tumors, we urgently need new and more effective diagnostic and therapeutic methods. In recent years, with the emergence of nanomaterials, multifunctional nanomaterials provide a new solution for the integration of tumor diagnosis and treatment. This multifunctional nanocarrier is a single nanomaterial with gaps that is simultaneously modified with a variety of biomolecules o...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K49/12A61K49/14A61K49/18A61K9/16A61K31/704A61K47/18A61K47/32A61P35/00
CPCA61K9/1676A61K31/704A61K47/183A61K47/32A61K49/126A61K49/14A61K49/1878
Inventor 朱春玲蒋有华柯淑娟曾胚羡谢增鸿
Owner FUZHOU UNIV