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Decoy nucleate cationic liposome carrier and preparation method thereof

A technology of cationic liposomes and blank liposomes, which is applied in the direction of liposome delivery, pharmaceutical formulations, non-effective ingredients of polymer compounds, etc., to achieve the effect of no cytotoxicity

Active Publication Date: 2015-09-23
JIANGSU KEYGEN BIOTECH CORP LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the prior art, there is no report about liposomes that assist drugs to enter the nucleus

Method used

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  • Decoy nucleate cationic liposome carrier and preparation method thereof
  • Decoy nucleate cationic liposome carrier and preparation method thereof
  • Decoy nucleate cationic liposome carrier and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Example 1 Preparation of Decoy nucleic acid cationic liposomes.

[0038] (1) Get DOPE, DOTAP each 3mg, be dissolved in 20ml chloroform and make lipid solution;

[0039] (2) Put the above lipid solution into a round-bottomed flask, rotate and evaporate under reduced pressure in a constant temperature water bath at 20°C, pay attention to the adjustment of the speed and temperature to avoid bubbles, remove the organic solvent, and form a lipid film, take 3ml 4mM pH 7.4 HEPES and add In the above-mentioned round bottom flask, hydrate at 20°C for 30 minutes, and then sonicate for 30 minutes after hydration, and the ultrasonic power is 100W to make a crude liposome solution; pass the crude liposome solution through a 0.4 μm membrane 10 times, and then through a 0.2 μm membrane 10 times Make 2mg / ml liposome solution.

[0040] (3) Take 2 mg of protamine and 1 mg of Decoy nucleic acid and dissolve them in 1 ml of 4mM pH 7.4 HEPES buffer respectively to prepare protamine and Dec...

Embodiment 2

[0043] Example 2 Preparation of Decoy nucleic acid cationic liposomes.

[0044] (1) Get DOPE, DOTAP each 3mg, be dissolved in 20ml chloroform and make lipid solution;

[0045] (2) Put the above lipid solution into a round-bottomed flask, rotate and evaporate under reduced pressure in a constant temperature water bath at 20°C, pay attention to the adjustment of the speed and temperature to avoid bubbles, remove the organic solvent, and form a lipid film, take 3ml 4mM pH 7.4 HEPES and add In the above-mentioned round bottom flask, hydrate at 20°C for 30 minutes, and then sonicate for 30 minutes after hydration, and the ultrasonic power is 100W to make a crude liposome solution; pass the crude liposome solution through a 0.4 μm membrane 10 times, and then through a 0.2 μm membrane 10 times Make 2mg / ml liposome solution.

[0046] (3) Take 2 mg of protamine and 1 mg of Decoy nucleic acid and dissolve them in 1 ml of 4mM pH 7.4 HEPES buffer respectively to prepare protamine and Dec...

Embodiment 3

[0049] Example 3 Preparation of Decoy nucleic acid cationic liposomes.

[0050] (1) Take DOPE 3mg, DOTAP 12mg, dissolve in 20ml chloroform to make lipid solution;

[0051] (2) Put the above lipid solution into a round-bottomed flask, rotate and evaporate under reduced pressure in a constant temperature water bath at 20°C, pay attention to the adjustment of the speed and temperature to avoid bubbles, remove the organic solvent, and form a lipid film, take 3ml 4mM pH 7.4 HEPES and add In the above-mentioned round bottom flask, hydrate at 20°C for 30 minutes, and then sonicate for 30 minutes after hydration, and the ultrasonic power is 100W to make a crude liposome solution; pass the crude liposome solution through a 0.4 μm membrane 10 times, and then through a 0.2 μm membrane 10 times Make 2mg / ml liposome solution.

[0052] (3) Take 2 mg of protamine and 1 mg of Decoy nucleic acid and dissolve them in 1 ml of 4mM pH 7.4 HEPES buffer respectively to prepare protamine and Decoy n...

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Abstract

The invention discloses a preparation method of a decoy nucleate cationic liposome carrier. The preparation method comprises the following steps: (1) mixing dioleoyl phosphoethanolamine and (2,3-di-oleoyl-propyl)-trimethylamine in a mass ratio of 4: 1 to 1: 4 to obtain a mixture, and dissolving the mixture in organic solvent to obtain a mixed solution; (2) completely evaporating the organic solvent in the mixed solution, dissolving remaining solids by utilizing an HEPES buffer solution, firstly hydrating the solution for 30 to 60 minutes, and then ultrasonically processing the solution for 30 to 60 minutes; (3) filtering a mixed system obtained after processing in the step (2) by virtue of a film of 0.4 to 0.8 micrometers, then filtering the mixed system by virtue of a film of 0.03 to 0.2 micrometers, and preparing uniformly-distributed blank liposome with small particle size; (4) mixing the blank liposome with protamine and Decoy nucleate according to a mass ratio of (50-120): (10-20): 1, and incubating for 12 to 24 hours at the temperature of 2 to 8 DEG C to form the complete decoy nucleate cationic liposome carrier. The Decoy nucleate cationic liposome is high in membrane penetrating rate and high in nucleate penetrating rate and has no cell toxicity.

Description

technical field [0001] The invention belongs to the technical field of pharmaceutical preparations, and in particular relates to a Decoy nucleic acid cationic liposome carrier and a preparation method thereof. Background technique [0002] Liposomes are ultrafine particles with a diameter of several nanometers to several micrometers formed by directional arrangement of phospholipid bimolecules, and fat-soluble and water-soluble drugs are respectively encapsulated inside and outside the bilayer. Liposomes have the characteristics of enabling drugs to be targeted, improving and prolonging curative effect, alleviating toxicity, avoiding drug resistance and changing the route of administration. Since the first application of liposomes as drug carriers by Rahman et al. in the 1960s, the research on the preparation process, mechanism of action, distribution in vivo, pharmacology and toxicology of liposomes has continued to deepen. [0003] Liposomes can be divided into neutral li...

Claims

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Application Information

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IPC IPC(8): A61K9/127A61K47/42A61K31/711A61P35/00
CPCA61K31/7088A61K9/0019A61K9/1272A61K9/127A61P35/00A61K31/711
Inventor 肖扬崔进龙李正荣叶青何凌云王雪根
Owner JIANGSU KEYGEN BIOTECH CORP LTD