Unlock instant, AI-driven research and patent intelligence for your innovation.

A method for hydrophilic modification of hydroxyapatite single crystal nanorods

A hydroxyapatite, single-crystal nanotechnology, applied in single-crystal growth, single-crystal growth, chemical instruments and methods, etc., can solve problems such as hydrophilicity limitations, and achieve stable product quality, good reproducibility, and raw materials. Inexpensive and accessible effects

Inactive Publication Date: 2018-01-23
NORTHWEST UNIV
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In order to obtain uniform nano-scale products of hydroxyapatite, the hydrophobic oleic acid reaction system is usually used to control the synthesis, and the surface of the obtained product is a hydrophobic surface, but its hydrophilicity is limited to a certain extent, so that it can be used in the biological field limitations

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A method for hydrophilic modification of hydroxyapatite single crystal nanorods
  • A method for hydrophilic modification of hydroxyapatite single crystal nanorods
  • A method for hydrophilic modification of hydroxyapatite single crystal nanorods

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] In a 100mL flask, add the above-mentioned 800mg hydrophobic hydroxyapatite nanorods, 200mg riboflavin sodium phosphate, and 50mL acetone solution, and reflux at 60°C for 6-8 h to obtain sample A; then use the phosphoric acid ligand in sample A Synthesize a new chain transfer agent with the functional group (-OH) on the chain transfer agent CTA, reaction conditions: 600mg product A and 108mg S-isocyanate-N-ethyl-N'-phenyldithiocarbamate (CTA) Use N,N'-dicyclohexylcarbodiimide (DCC, 1.00g) as a dehydrating agent, 4-dimethylaminopyridine (DMAP, 200mg) as a catalyst to form a new chain transfer agent, and react at room temperature for 18- 24 h is recorded as sample B. Finally, 100mg of sample B was used as a new chain transfer agent, 12mg of azobisisobutyronitrile (AIBN) as a chain initiator, 1.00g of hydrophilic polymer polyethylene glycol methacrylate (PEGMA) as a monomer, tetrahydrofuran As a solvent, react for 24 h under nitrogen atmosphere, and collect samples.

[00...

Embodiment 2

[0026] In a 100mL flask, add 800mg hydrophobic hydroxyapatite nanorods, 200mg riboflavin sodium phosphate, and 50mL acetone solution, and reflux at 60°C for 6-8 h to obtain sample A; The functional group (-OH) of the chain transfer agent CTA to synthesize a new chain transfer agent, reaction conditions: 600mg product A and 108mg S-isocyanate-N-ethyl-N'-phenyldithiocarbamate ( CTA) Use N,N'-dicyclohexylcarbodiimide (DCC, 1.00g) as a dehydrating agent, 4-dimethylaminopyridine (DMAP, 200mg) as a catalyst to form a new chain transfer agent, and react at room temperature for 18-24 h is recorded as sample B. Finally, 100mg of sample B was used as a new chain transfer agent, 12mg of azobisisobutyronitrile (AIBN) as a chain initiator, 2.00g of hydrophilic polymer polyethylene glycol methacrylate (PEGMA) as a monomer, tetrahydrofuran As a solvent, react for 24 h under nitrogen atmosphere, and collect samples.

Embodiment 3

[0028] In a 100mL flask, add 800mg hydrophobic hydroxyapatite nanorods, 200mg riboflavin sodium phosphate, and 50mL acetone solution, and reflux at 60°C for 6-8 h to obtain sample A; The functional group (-OH) of the chain transfer agent CTA to synthesize a new chain transfer agent, reaction conditions: 600mg product A and 108mg S-isocyanate-N-ethyl-N'-phenyldithiocarbamate ( CTA) Use N,N'-dicyclohexylcarbodiimide (DCC, 1.00g) as a dehydrating agent, 4-dimethylaminopyridine (DMAP, 200mg) as a catalyst to form a new chain transfer agent, and react at room temperature for 18-24 h is recorded as sample B. Finally, the sample 100mg B was used as a new chain transfer agent, 12mg azobisisobutyronitrile (AIBN) was used as a chain initiator, 1.00g hydrophilic polymer phospholipid was used as a monomer, tetrahydrofuran was used as a solvent, and the reaction was carried out under nitrogen atmosphere for 24 h. Collect samples.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
Login to View More

Abstract

The invention discloses a hydrophilic modification method of hydroxyapatite single crystal nanorods. First, surface oleic acid-modified hydroxyapatite nanocrystals are synthesized, and then the surface oleic acid-modified hydroxyapatite nanocrystals are combined with Nucleotide 5'-monophosphate adenosine sodium salt or riboflavin sodium phosphate was refluxed in acetone solvent at a mass ratio of 4:1 to perform surface ligand exchange to prepare sample A, sample A and S-isocyanate- The reaction of N-ethyl-N'-phenyldithiocarbamate resulted in sample B of hydroxyapatite nanocrystals surface-modified with a chain transfer agent. Sample B underwent reversible addition-fragmentation chain transfer with hydrophilic polymers. Polymerization reaction is enough. The hydrophilic nanohydroxyapatite prepared by the method of the present invention can be used for drug delivery, cell imaging, and can also be used as an inorganic raw material to prepare biomedical materials such as degradable artificial bone and bone cement. It has good application prospects in engineering and other related fields.

Description

technical field [0001] The invention relates to a method for modifying the hydrophilicity of hydroxyapatite single crystal nanorods. Background technique [0002] With the development of life sciences, people hope to obtain rich and detailed intuitive information about tissues, cells, etc., prompting the rapid development of various imaging technologies. Among them, the hydrophilicity of materials is very important, which affects the absorption of materials by cells and animals, thus restricting the application of materials. [0003] Hydroxyapatite (Ca 10 (OH) 2 (PO 4 ) 6 , HAp) have excellent biocompatibility, osteoinductivity, non-immunogenicity, degradability and other properties, and are widely used in tissue engineering, drug and gene delivery and other biological fields. At the same time, hydroxyapatite is also a good ion-doped matrix material, which is often endowed with new physical and chemical properties by impurity ions. In order to obtain uniform nano-scale...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C30B29/60C30B7/00C30B33/00
Inventor 衡春宁郑晓燕张小勇范代娣惠俊峰
Owner NORTHWEST UNIV