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Preparation method of oxygen-producing particles of calcium peroxide coated with polylactic acid-glycolic acid copolymer

A glycolic acid copolymer, calcium peroxide technology, applied in medical science, prosthesis, etc., can solve difficult to meet the needs of tissue regeneration, oxygen-producing particles without good biocompatibility and degradability, oxygen-producing time maintenance, etc. question

Inactive Publication Date: 2022-02-25
NINGBO MEDICAL CENT LIHUILI HOSPITACL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Oxygen-producing particles have been widely used in tissue engineering and drug carriers, but the existing oxygen-producing particles do not have good biocompatibility and degradability, and it is difficult to be non-toxic, non-irritating and non-immunogenic. Kinetic instability, short oxygen production time, difficult to meet the needs of tissue regeneration

Method used

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  • Preparation method of oxygen-producing particles of calcium peroxide coated with polylactic acid-glycolic acid copolymer
  • Preparation method of oxygen-producing particles of calcium peroxide coated with polylactic acid-glycolic acid copolymer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] 1) Exissue the polylactic acid-hydroxyacetic acid copolymer in dichloromethane to prepare 10 ml of 5% (w / v) PLGA solution; dissolve gelatin in deionized water to prepare 150 ml of 1% (w / v) gelatin solution; 2 Add 1 ml 2% (w / v) CaO in deionized water 2 Suspension;

[0021] 2) CAO prepared by step 1) 2 The suspension is mixed with a PLGA solution and homogeneous treatment to obtain the first mixture;

[0022] 3) In the gelatin solution prepared in step 1), the first mixture prepared in step 2 is added to obtain a second mixture, and the second mixed liquid homogen is treated with the heating magnetic stirrer to heat it for 4 hours to evaporate removal. The remaining dichloromethane was centrifuged to discard the supernatant, and the oxygen-oxidant particles were washed.

[0023] The specific steps of the sediment washing process in the step 3) are as follows:

[0024] a) Place the precipitate in a test tube containing 30 ml of methanol, mix well for 60 seconds, stand fo...

Embodiment 2

[0029] 1) Dissolve the polylactic acid-hydroxyacetic acid copolymer in dichloromethane to prepare 10 ml of 4.5% (w / v) PLGA solution; dissolve gelatin in deionized water to prepare 150 ml of 1% (w / v) gelatin solution; 2 Add 1 ml 1.5% (w / v) CAO in deionized water 2 Suspension;

[0030] 2) CAO prepared by step 1) 2 The suspension is mixed with a PLGA solution and homogeneous treatment to obtain the first mixture;

[0031] 3) In the gelatin solution prepared in step 1), the first mixture prepared in step 2 is added to obtain a second mixture, and the second mixed liquid homogen is treated with the heating magnetic stirrer to heat it for 3 hours to evaporate removal. The remaining dichloromethane was centrifuged to discard the supernatant, and the oxygen-oxidant particles were washed.

[0032] The specific steps of the sediment washing process in the step 3) are as follows:

[0033] a) Place the precipitate in a test tube containing 30 ml of methanol, mix well for 60 seconds, sta...

Embodiment 3

[0037] 1) Dissolve the polylactic acid-hydroxyacetic acid copolymer in dichloromethane to prepare 10 ml of 5.5% (w / v) PLGA solution; dissolve gelatin in deionized water to prepare 150 ml of 2% (w / v) gelatin solution; 2 Add 1 mL 2.5% (w / v) CAO in deionized water 2 Suspension;

[0038] 2) CAO prepared by step 1) 2 The suspension is mixed with a PLGA solution and homogeneous treatment to obtain the first mixture;

[0039] 3) In the gelatin solution prepared in step 1), the first mixture prepared in step 2 is added to obtain a second mixture, and the second mixed liquid homogen is treated with the heating magnetic stirrer to heat it for 4 hours to evaporate removal. The remaining dichloromethane was centrifuged to discard the supernatant, and the oxygen-oxidant particles were washed.

[0040] The specific steps of the sediment washing process in the step 3) are as follows:

[0041]a) Place the precipitate in a test tube containing 30 ml of methanol, mix well for 60 seconds, stan...

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Abstract

The invention relates to the technical field of biomedical materials, and particularly discloses a preparation method of oxygen-producing particles with calcium peroxide coated with a polylactic acid-glycolic acid copolymer. The oxygen-producing particles prepared by the method are CPO particles with the outer layer coated with PLGA, the polylactic acid-glycolic acid copolymer on the outer layer is a high-molecular organic polymer, has good biocompatibility and degradability, is non-toxic, non-irritant and non-immunogenicity, and can be completely degraded into lactic acid and glycolic acid in a living body finally, and the two degradation products are byproducts of human metabolic pathways, so that the oxygen-producing particles have no toxic or side effect when being applied to medicines and biological materials.

Description

Technical field [0001] The present invention relates to the technical field of biomedical materials, and is specifically a method for producing an oxygenated product of a polylactic acid-hydroxyacetic acid copolymer package being peroxide. Background technique [0002] Biological tissue engineering, a small amount of living tissue is obtained from the body, and the cells (also known as seed cells) are separated from the tissue from tissues in vitro by special enzymes or other methods, and the amplified cells are combined with a good biology phase. Composition, degradability, and absorbable biomaterials (brackets) are mixed in a certain proportion of cells to form a cell-material complex on a biomaterial (stent); the complex is implanted into the body or organ disease The damage is gradually degraded and absorbed in the body, and the implanted cells continue to proliferate and secrete the extracellular matrix, and finally form the corresponding tissue or organ, thereby achieving t...

Claims

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Application Information

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IPC IPC(8): A61L27/18A61L27/02A61L27/22A61L27/50A61L27/54A61L27/58
CPCA61L27/18A61L27/025A61L27/222A61L27/50A61L27/54A61L27/58A61L2300/602A61L2300/412C08L67/04
Inventor 干开丰吴畏李杰张挺徐顶立李瑾
Owner NINGBO MEDICAL CENT LIHUILI HOSPITACL