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Injectable protein hydrogel stent and application thereof in prolonging in-vivo stability of drug

A hydrogel and protein technology, applied in the application field of injectable protein hydrogel scaffolds and prolonging the stability of drugs in vivo, can solve the problems of unfavorable gel fixed-point molding tolerance, poor biocompatibility and biodegradability and other problems, to achieve good volume support effect, prolong the stability in the body, and fast coagulation speed

Pending Publication Date: 2021-03-19
NANTONG UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, most of the existing injectable hydrogels have poor biocompatibility and biodegradability, which is not conducive to the fixed-point molding of the gel after injection and the tolerance problems caused by long-term exercise.

Method used

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  • Injectable protein hydrogel stent and application thereof in prolonging in-vivo stability of drug
  • Injectable protein hydrogel stent and application thereof in prolonging in-vivo stability of drug
  • Injectable protein hydrogel stent and application thereof in prolonging in-vivo stability of drug

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Effects of hydrogel decomposition on the body:

[0044] Preparation process of injectable protein hydrogel:

[0045] Accurately weigh 16mg of Fmoc-Phe and 12mg of Phe2 and slowly add it to the mixed solution of 1mL PBS (pH 7.4) and 420μL of 0.5mol / L NaOH and stir slowly until it is completely dissolved. At this time, the final concentration of the solution is Fmoc-Phe11.3mg / mL and Phe2 8.5mg / mL. Adjust the pH to 7.0 with 0.1 mol / L HCl solution, and the volume of the solution is about 3.5 mL. Pseudomonas fluorescens lipase (PFL) was completely dissolved in PBS (pH 7.4) to prepare 100 μL of a 50 mg / mL PFL solution. Slowly add the prepared PFL solution into the amino acid hydrogel precursor solution and mix well.

[0046] The prepared hydrogel sample was transferred to a quartz glass slide, and the sample was fully dehydrated and dried using a vacuum dryer, then ground, and the Fourier transform infrared (FTIR) spectrum of the hydrogel dry powder was measured and record...

Embodiment 2

[0049] The light transmittance of hydrogel with a thickness of 1cm at different wavelengths:

[0050] Preparation process of injectable protein hydrogel:

[0051] The amino acid hydrogel sample is placed in the detection cell, and the UV spectrum is recorded with an ultraviolet-visible spectrophotometer, and the wavelength range of the recorded spectrum is from 200nm to 1000nm. The light transmittance of the current wavelength can be calculated from the absorbance value corresponding to the wavelength.

[0052] Such as figure 2 Shown is the transmittance at different wavelengths of the hydrogel with a thickness of 1cm. It can be seen from the figure that at the ICG absorption wavelength peak at 808nm, the transmittance of the amino acid hydrogel with a thickness of 1cm (light path of the cuvette) is about 84.5 %, has higher light transmission ability.

Embodiment 3

[0054] Injectable hydrogel scaffold entrapped red blood cell-insulin:

[0055] Preparation process of erythrocyte-insulin hydrogel:

[0056] Accurately weigh 16mg of Fmoc-Phe and 12mg of Phe2 and slowly add it to the mixed solution of 1mL PBS (pH 7.4) and 420μL of 0.5mol / L NaOH and stir slowly until it is completely dissolved. At this time, the final concentration of the solution is Fmoc-Phe11.3mg / mL and Phe2 8.5mg / mL. Adjust the pH to 7.0 with 0.1 mol / L HCl solution, and the volume of the solution is about 3.5 mL.

[0057] Pseudomonas fluorescens lipase (PFL) was completely dissolved in PBS (pH 7.4) to prepare 100 μL of 50 mg / mL PFL solution. Slowly add the prepared PFL solution into the amino acid hydrogel precursor solution and mix well.

[0058] Take 1 mL of insulin-loaded red blood cells and add amino acid hydrogel precursor solution in an appropriate volume ratio, then add 100 μl of 50 mg / mL PFL solution, mix slowly, and place in a constant temperature water bath at 3...

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Abstract

The invention provides an injectable protein hydrogel stent and an application thereof in prolonging in-vivo stability of a drug. The hydrogel is prepared from Fmoc-Phe and Ph2, and is mixed with a pseudomonas fluorescens lipase (PFL) solution to prepare an amino acid hydrogel precursor. The invention has beneficial effects that the injectable protein hydrogel stent has a good volume stent effect,can provide a supporting effect for 5-7 days and then is completely metabolized by a body, and meanwhile, the injectable protein hydrogel stent can prolong clearance of the body to a drug after subcutaneous injection, and can also inhibit infiltration of macrophages, thereby reducing inflammatory response in the injection area.

Description

technical field [0001] The invention relates to the technical field of an injectable protein hydrogel stent, which can be used as a drug carrier to prolong the action time of the drug through subcutaneous injection, and in particular to an injectable protein hydrogel stent and its application for prolonging the stability of the drug in vivo. Background technique [0002] Hydrogels are hydrophilic, water-swellable polymer networks formed from the synthetic building blocks of a variety of natural and synthetic polymers. These synthetic building blocks are engineered to be cross-linked through chemical reactions or physical interactions of cells and proteins, allowing rapid injection or formation of in situ hydrogels in the process. However, most of the existing injectable hydrogels have poor biocompatibility and biodegradability, which is not conducive to the fixed-point molding of the gel after injection and the tolerance problems caused by long-term exercise. [0003] How t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K38/28A61K9/50A61K47/46A61K9/06A61K47/42A61P3/10A61K31/409
CPCA61K38/28A61K31/409A61K9/5068A61P3/10A61K9/0024A61K47/42A61K9/06A61K2300/00
Inventor 夏栋林鲍鸿一陈静茹马乾蒋肖含王馨蓉
Owner NANTONG UNIVERSITY