Nano-hydroxyapatite/carboxymethyl chitosan/poly(lactic-co-glycolic acid) micro-nano hybrid drug-loaded scaffold and bionic preparation method thereof

A nano-hydroxyapatite, carboxymethyl chitosan technology, applied in medical science, tissue regeneration, prosthesis, etc., can solve the problem of poor hydrophilicity and biocompatibility, lack of cell recognizable sites, lack of Biological activity and other issues, to achieve the effect of improving biological activity, good biocompatibility, and achieving complementary functional advantages

Active Publication Date: 2017-11-21
FUZHOU UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, such materials also have disadvantages such as poor hydrophilicity and biocompatibility, lack of cell-recognizable sites, degradation products may cause aseptic inflammation, and generally have no biolo

Method used

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  • Nano-hydroxyapatite/carboxymethyl chitosan/poly(lactic-co-glycolic acid) micro-nano hybrid drug-loaded scaffold and bionic preparation method thereof
  • Nano-hydroxyapatite/carboxymethyl chitosan/poly(lactic-co-glycolic acid) micro-nano hybrid drug-loaded scaffold and bionic preparation method thereof
  • Nano-hydroxyapatite/carboxymethyl chitosan/poly(lactic-co-glycolic acid) micro-nano hybrid drug-loaded scaffold and bionic preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0039] Example 1

[0040] 1) Disperse 0.075 g of nano-hydroxyapatite in 20 mL of deionized water, and sonicate for 10 minutes to make the dispersion uniform;

[0041] 2) Add 0.2g of carboxymethyl chitosan to it and stir for 1 hour with a magnetic stirrer to form a uniform water phase (continuous phase);

[0042] 3) Take 136 µg of icariin and add it to the above water phase to prepare a molar concentration of 10 -5 Icariin solution of M;

[0043] 4) Dissolve 0.32g of polylactic acid glycolic acid in 8mL of dichloromethane to prepare the oil phase (dispersed phase) of the emulsion;

[0044] 5) Take 5mL of the emulsion water phase and 2mL of the oil phase, add them to the mold, add 14.5 µL of glutaraldehyde to the mold with the molar ratio of amino group to aldehyde group at 1:1, and use Ultra Turrax T25 high-speed emulsifier 3 Emulsify at rpm / min, the emulsification time is 1min;

[0045] 6) Put the emulsion at room temperature for 12h to volatilize the solvent, then transfer it to -10~-8...

Example Embodiment

[0046] Example 2

[0047] 1) Disperse 0.15g of nano-hydroxyapatite in 20mL of deionized water, and ultrasound for 10min to make the dispersion uniform;

[0048] 2) Add 0.2g of carboxymethyl chitosan to it and stir for 1 hour with a magnetic stirrer to form a uniform water phase (continuous phase);

[0049] 3) Take 136 µg of icariin and add it to the above water phase to prepare a molar concentration of 10 -5 Icariin solution of M;

[0050] 4) Dissolve 0.32g polylactic acid glycolic acid in 8mL dichloromethane to prepare the oil phase (dispersed phase) of the emulsion;

[0051] 5) Take 5mL of the emulsion water phase and 2mL of the oil phase, add them to the mold, add 14.5 µL of glutaraldehyde to the mold with the molar ratio of amino group to aldehyde group at 1:1, and use Ultra Turrax T25 high-speed emulsifier 3 Emulsify at rpm / min, the emulsification time is 1min;

[0052] 6) Place the emulsion at room temperature for 12h to volatilize the solvent, then transfer it to -10~-80℃ for fre...

Example Embodiment

[0053] Example 3

[0054] 1) Disperse 0.3 g of nano-hydroxyapatite in 20 mL of deionized water, and sonicate for 10 minutes to make the dispersion uniform;

[0055] 2) Add 0.2g of carboxymethyl chitosan to it and stir for 1 hour with a magnetic stirrer to form a uniform water phase (continuous phase);

[0056] 3) Take 136 µg of icariin and add it to the above water phase to prepare a molar concentration of 10 -5 Icariin solution of M;

[0057] 4) Dissolve 0.32g polylactic acid glycolic acid in 8mL dichloromethane to prepare the oil phase (dispersed phase) of the emulsion;

[0058] 5) Take 5mL of the emulsion water phase and 2mL of the oil phase, add them to the mold, add 14.5 µL of glutaraldehyde to the mold with the molar ratio of amino group to aldehyde group at 1:1, and use Ultra Turrax T25 high-speed emulsifier 3 Emulsify at rpm / min, the emulsification time is 1min;

[0059] 6) Place the emulsion at room temperature for 12h to volatilize the solvent, then transfer it to -10~-80℃ for...

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Abstract

The invention belongs to the field of composite materials, and concretely relates to a nano-hydroxyapatite/carboxymethyl chitosan/poly(lactic-co-glycolic acid) micro-nano hybrid drug-loaded scaffold and a bionic preparation method thereof. The three-dimensional bionic hybrid drug-loaded scaffold is prepared through combining solvent evaporation and freeze drying technologies by using a high speed emulsifying machine via adopting nano-hydroxyapatite and carboxymethyl chitosan as a water phase and an emulsion continuous phase, adopting a methylene chloride solution of poly(lactic-co-glycolic acid) as an oil phase and an emulsion dispersion phase, using glutaraldehyde as a cross-linking agent to immobilize the carboxymethyl chitosan in the continuous phase and adopting the main component icariin in a traditional Chinese medicine epimeddium as a carrier drug. The preparation method has the advantages of simple preparation process and mild reaction conditions, and the obtained scaffold overcomes the performance defects of single natural polymer materials or synthetic polymer materials, has the advantages of intercommunicated pores, uniform pore diameter, figurability, slow drug release, good bone bonding ability and good biocompatibility, and is expected to become a new osteoporosis treatment composite material.

Description

technical field [0001] The invention belongs to the field of composite materials, and in particular relates to a nano-hydroxyapatite / carboxymethyl chitosan / polylactic acid glycolic acid micro-nano hybrid drug-loaded support and a bionic preparation method thereof. Background technique [0002] In recent years, with the extension of life expectancy and the aggravation of population aging, osteoporosis has become one of the important diseases affecting human health. Osteoporosis is a series of skeletal lesions caused by various reasons. It is a systemic skeletal disease characterized by low bone mass per unit volume and destruction of bone tissue microstructure. Accompanied by the aggravation of bone loss, the bone density of patients gradually decreases. , Bone fragility increases, greatly increasing the probability of fractures in patients, and its clinical manifestations are bone pain and fractures. According to the estimates of the World Health Organization, about 200 mil...

Claims

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Application Information

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IPC IPC(8): A61L27/48A61L27/42A61L27/54A61L27/56A61L27/58
CPCA61L27/425A61L27/48A61L27/54A61L27/56A61L27/58A61L2300/232A61L2300/412A61L2300/602A61L2430/02C08L5/08C08L67/04
Inventor 陈景帝胡义敏赵耀李倩张其清
Owner FUZHOU UNIVERSITY
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