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Preparation method of liposome emulsion

A liposome and emulsion technology, which is applied in the directions of liposome delivery, medical preparations containing inactive ingredients, and medical preparations containing active ingredients, etc., can solve problems such as environmental pollution, product solvent residues, and impact on product quality, etc., To achieve the effect of simple preparation equipment and process, safe and environmentally friendly production process, and high product safety

Pending Publication Date: 2021-10-01
HUAANTANG BIOTECH GRP CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The introduction of organic solvents may cause risks such as environmental pollution and product solvent residues, which directly affect the quality of products. Therefore, strict control and management are required in industrial production
Moreover, except for the film method, other traditional liposome preparation methods are generally not suitable for large-scale industrial production, thus limiting the promotion and application of liposomes in industrialization

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  • Preparation method of liposome emulsion
  • Preparation method of liposome emulsion
  • Preparation method of liposome emulsion

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0069] In this embodiment, the preparation formula of glabridin liposome is shown in Table 1, and the specific preparation steps are as follows:

[0070] (1) Add phospholipids (PC95%), glabridin and cholesterol to the prescribed amount of water, heat in a water bath at 60°C, and use an experimental IKA high-speed shear disperser to shear at a speed of 10,000 rpm for 60 minutes to obtain a uniform emulsion.

[0071] (2) Homogenize the homogeneous emulsion obtained in the step (1) under high pressure, and circulate twice under the pressure of 400 / 600 / 800 / 1000 bar respectively to obtain uniform glabridin liposomes.

[0072] Such as Figure 12 As shown, the particle size of the liposomes in the emulsion obtained in step (1) of this example is about 10 to 20 microns, indicating that the high-speed shear sample has not reached the nanometer level at this time, and the fat-soluble drug is emulsified and dissolved in the in the water.

[0073] From figure 1 It can be seen that afte...

Embodiment 2

[0075] In this embodiment, the preparation formula of glabridin liposome is shown in Table 1, and the specific preparation steps are as follows:

[0076] (1) Add phospholipids (PC95%), glabridin and cholesterol to the prescribed amount of water, heat in a water bath at 60°C, and use an experimental IKA high-speed shear disperser to shear at a speed of 10,000 rpm for 60 minutes to obtain a uniform emulsion.

[0077] (2) Homogenize the homogeneous emulsion obtained in the step (1) under high pressure, and circulate twice under the pressure of 400 / 600 / 800 / 1000 bar respectively to obtain uniform glabridin liposomes.

[0078] From figure 2 It can be seen that after high-speed shearing in step 1, a liposome-like multilayer spherical structure can be observed in the emulsion in step 1.

[0079] Such as Figure 13 As shown, the particle size of the liposomes in the emulsion obtained in step (1) of this example is about 4 to 10 microns, indicating that the high-speed shear sample ha...

Embodiment 3

[0081] In this embodiment, the preparation formula of glabridin liposome is shown in Table 1, and the specific preparation steps are as follows:

[0082] (1) Add phospholipids (PC95%), glabridin and cholesterol to the prescribed amount of water, heat in a water bath at 60°C, and use an experimental IKA high-speed shear disperser to shear at a speed of 10,000 rpm for 60 minutes to obtain a uniform emulsion.

[0083] (2) Homogenize the homogeneous emulsion obtained in the step (1) under high pressure, and circulate twice under the pressure of 400 / 600 / 800 / 1000 bar respectively to obtain uniform glabridin liposomes.

[0084] From image 3 It can be seen that after high-speed shearing in step 1, a liposome-like multilayer spherical structure can be observed in the emulsion in step 1.

[0085] Such as Figure 14 As shown, the particle size of the liposomes in the emulsion obtained in step (1) of this example is about 4 to 8 microns, indicating that the high-speed shear sample has ...

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Abstract

The invention relates to the technical field of lipidosome, in particular to a preparation method of lipidosome emulsion. The invention discloses a preparation method of a liposome emulsion, and the method comprises the following steps: mixing phospholipid, an insoluble drug and water to obtain a turbid liquid, dispersing the turbid liquid through high-speed shearing at a proper temperature, and crushing the phospholipid and the insoluble drug to form a micron scale. Under the micron scale, after long-time shearing, insoluble drug particles and phospholipid particles interact with each other to generate emulsification, and then self-assembly is performed to form the micron-sized liposome. The preparation method does not use toxic and harmful organic solvents, the production process is safe and environment-friendly, and the product safety is high; the preparation equipment and process are simple, large-scale production is facilitated, and the production efficiency is improved.

Description

technical field [0001] The invention relates to the technical field of liposomes, in particular to a preparation method of liposome emulsion. Background technique [0002] In recent years, the application of liposomes has attracted more and more attention, and has been widely used in biomedicine, cosmetics, health food and other fields. [0003] There are many methods for preparing fat-soluble drug liposomes, such as thin film method, reverse phase evaporation method, injection method, etc. Most of the preparation methods involve the use of organic solvents. The introduction of organic solvents may cause risks such as environmental pollution and product solvent residues, and directly affect the quality of products. Therefore, strict control and management are required in industrial production. Moreover, except for the thin-film method, other traditional liposome preparation methods are generally not suitable for large-scale industrial production, thereby limiting the promot...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/127A61K45/00A61K31/352A61K47/10A61K47/24A61K47/14B82Y40/00B82Y5/00
CPCA61K9/127A61K45/00A61K31/352A61K47/10A61K47/24A61K47/14B82Y40/00B82Y5/00
Inventor 卢永杰程路诗张炽坚张兵江桦关焕敏艾勇何廷刚
Owner HUAANTANG BIOTECH GRP CO LTD