A kind of microencapsulated animal drug and preparation method thereof

A technology for medicines and animals, applied in microcapsules, pharmaceutical formulations, inactive components of polymer compounds, etc. It can solve the problems of inapplicability of easily oxidized and heat-sensitive materials, inability to meet the requirements of assembly lines, and irregular product particles. , to achieve good market prospects, improve production efficiency, and achieve the effect of particle rounding

Active Publication Date: 2020-05-26
GUANGDONG WENS DAHUANONG BIOTECH
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, there are three main methods for preparing microencapsulated drugs: one is the boiling granulation method, in which the powdery material is put into a closed container, and due to the action of hot air flow, the powdery material is suspended in a fluidized state in the container, and sprayed into the container at the same time. The binder is atomized to make the powder agglomerate into small particles, but the production equipment of this method is mostly batch production, which cannot meet the requirements of the assembly line, and the product particles are irregular, which is not suitable for easily oxidized and heat-sensitive materials. Not applicable
The second is the fluidized bed coating method, which is the main method for forming powdery and crystalline drugs into microcapsules based on physical and mechanical principles, but the coated drugs have a large specific surface area, and particles often occur during the preparation process. The phenomenon of adhesion and electrostatic adsorption, and the coating process takes a long time, consumes a lot of energy, high production cost and low production efficiency
For example, the document "Research on the Preparation and Properties of Tiamulin Fumarate Taste-masking Microcapsules" (first author: Han Jing) discloses that gelatin, β-cyclodextrin and castor oil are used as auxiliary materials and prepared by spray-drying method. Tiamulin fumarate microcapsules can effectively cover up the unpleasant smell of the API, and improve the hygroscopicity and fluidity of the microcapsules, but it also points out that the process is prone to sticking to the wall during the spray drying process
Another example is the patent document CN105287433A which discloses a preparation method of microencapsulated animal medicines. The method uses gelatin, sugars, β-cyclodextrin, and castor oil as auxiliary materials, which can also achieve taste masking, moisture resistance, and improve the bioavailability of drugs. The purpose of high efficiency, but its microemulsion contains more sugars, and the material has relatively strong cohesiveness, so the problem of sticking to the wall is more likely to occur during the spray drying process

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 kind of microencapsulated animal drug and preparation method thereof
  • A kind of microencapsulated animal drug and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Embodiment 1, microencapsulated animal drug of the present invention and preparation method thereof

[0034] Formula: tilmicosin 25kg, gelatin 30kg, sucrose 40kg, Tween-80 5kg, corn starch 30kg, microcrystalline cellulose 3kg;

[0035] Preparation:

[0036] S1. Preparation of wall materials: dissolve gelatin and sucrose in 200 kg of water to obtain water phase A;

[0037] S2, preparation of capsule material: dissolve tilmicosin in 300kg water, then add Tween-80 to obtain oil phase B;

[0038] S3. Preparation of dispersion system: under the conditions of shear power of 50kW and stirring speed of 10000r / min, the oil phase B was added to the water phase A, and then the stirring time was 15min and the temperature was 50°C Under certain conditions, part of the water is removed to form a microemulsion;

[0039] S4, spray granulation and drying: in the spray granulation tower, add the mixed filler of the cornstarch of formula quantity and microcrystalline cellulose, then pu...

Embodiment 2

[0041] Embodiment 2, microencapsulated animal drug of the present invention and preparation method thereof

[0042] Formula: tiamulin fumarate 30kg, gelatin 30kg, glucose 35kg, Tween-80 5kg, corn starch 40kg, microcrystalline cellulose 8kg;

[0043] Preparation:

[0044] S1. Preparation of wall materials: dissolve gelatin and glucose in 200 kg of water to obtain water phase A;

[0045] S2. Preparation of capsule material: dissolve tiamulin fumarate in 400 kg of ethanol with a volume fraction of 85%, and then add Tween-80 to obtain oil phase B;

[0046] S3. Preparation of dispersion system: under the conditions of shear power of 50kW and stirring speed of 5000r / min, the oil phase B was added to the water phase A, and then the stirring time was 15min and the temperature was 50°C Under the conditions, ethanol is removed to form a microemulsion;

[0047] S4, spray granulation and drying: in the spray granulation tower, add the mixed filler of the cornstarch of formula quantity an...

Embodiment 3

[0049] Embodiment 3, microencapsulated animal drug of the present invention and preparation method thereof

[0050] Formula: enrofloxacin sodium 25kg, gelatin 30kg, sucrose 40kg, Tween-80 5kg, rice bran 35kg, microcrystalline cellulose 5kg;

[0051] Preparation:

[0052] S1. Preparation of wall materials: dissolve gelatin and sucrose in 200 kg of water to obtain water phase A;

[0053] S2. Preparation of capsule material: dissolving enrofloxacin sodium in 300kg of water, then adding Tween-80 to obtain oil phase B;

[0054] S3. Preparation of dispersion system: under the conditions of shear power of 80kW and stirring speed of 5000r / min, the oil phase B was added to the water phase A, and then the stirring time was 20min and the temperature was 50°C Under certain conditions, part of the water is removed to form a microemulsion;

[0055] S4. Spray granulation and drying: Add the mixed filler of rice bran and microcrystalline cellulose in the formula amount into the spray granu...

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
particle sizeaaaaaaaaaa
Login to view more

Abstract

The invention relates to the technical field of veterinary drugs, in particular to a microencapsulated animal drug and a preparation method thereof. The microencapsulated animal medicine comprises a raw material medicine, a wall material and an external filler. The wall material is prepared from the following preparation raw materials in parts by weight: 30-40 parts of gelatin and 30-50 parts of saccharides; and the external filler comprises the following preparation raw materials in parts by weight: 30-40 parts of corn starch or rice bran and 3-8 parts of microcrystalline cellulose. Accordingto the invention, external auxiliary materials are applied to effectively solve the problem of wall sticking in a spray drying process; the microencapsulated animal medicine has the characteristics of round particles, good capsule material coating effect and good free-flowing property, and effective medicine components are isolated from the outside, so that the purposes of masking taste, preventing moisture, improving medicine stability and improving medicine utilization rate are achieved.

Description

technical field [0001] The invention relates to the technical field of veterinary medicine, in particular to a microencapsulated animal medicine and a preparation method thereof. Background technique [0002] Microcapsule technology is a technology that uses natural or synthetic polymer film-forming materials (wall materials) to embed liquid or solid drugs (capsule materials) to form microcapsule particles with a diameter of 100-500 μm. The process of preparing microcapsule particles Referred to as microencapsulation. Drug microencapsulation has the advantages of masking the bitter or peculiar smell of drugs, improving drug fluidity and hygroscopicity, improving drug stability, controlling drug release, and reducing gastrointestinal irritation. Therefore, the preparation method of microencapsulated drugs has become very popular at present. , are widely used in various industries. [0003] At present, there are three main methods for preparing microencapsulated drugs: one i...

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): A61K9/50A61K47/42A61K47/26A61K47/36A61K47/38A61K31/706A61K31/496A61K31/165A61K31/22
CPCA61K9/5015A61K9/5036A61K9/5042A61K9/5057A61K31/165A61K31/22A61K31/496A61K31/706
Inventor 张桂君方炳虎吴志玲梁劲康黎健业颜振炽汤钦
Owner GUANGDONG WENS DAHUANONG BIOTECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products