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A kind of preparation method of florfenicol superfine powder

A technology of florfenicol and superfine powder, which is applied in the field of preparation of florfenicol superfine powder, can solve the problems of local irritation and toxic reaction, inconvenient application of injection, unreliable safety and other problems, and achieve excellent dispersion Stabilizing effect, excellent micro effect, effect of lowering temperature

Active Publication Date: 2021-07-06
京山瑞生制药有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

And injection is difficult to be applied on a large scale in large-scale farms due to inconvenient application.
Moreover, most of the injections are prepared with organic solvents such as dimethylformamide and propylene glycol, which are likely to cause local irritation and toxicity, and are unreliable in safety.
[0006] At present, the preparation of florfenicol superfine powder has become the development trend of the industry, but florfenicol products are easy to crystallize, and it is very difficult to obtain superfine powder products
The ultrafine pulverization equipment common in the industry is not only inefficient, but also the particle size of the obtained micropowder is generally larger than 20 microns

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] (1) In the reactor, add solvent acetone, dissolve the former powder of florfenicol in acetone, be mixed with the acetone solution of florfenicol, wherein the concentration of florfenicol is 30mg / ml.

[0026] (2) In another reactor, prepare sodium chloride brine solution, wherein the concentration of sodium chloride salt is 10%.

[0027] (3) Turn on the strong stirring of the sodium chloride saline solution, control the temperature at 0°C, and quickly pump the acetone solution of Florfenicol into the liquid surface of the saline solution through a high-pressure delivery pump, and the flow rate at the outlet pipe greater than 3 m / s. Continue vigorous stirring for 30 min. A suspension of florfenicol was obtained. Wherein the volume ratio of the saline solution to the acetone solution of Florfenicol is 5:1.

[0028] (4) The suspension is subjected to solid-liquid separation, and the florfenicol superfine powder product can be obtained after drying. The obtained florfeni...

Embodiment 2

[0030] (1) In the reaction kettle, add solvent acetone, dissolve the former powder of Florfenicol in acetone, be mixed with the acetone solution of Florfenicol, wherein the concentration of Florfenicol is 100mg / ml.

[0031] (2) In another reactor, potassium chloride brine solution is prepared, wherein the salt concentration is saturated.

[0032] (3) Turn on the vigorous stirring of the potassium chloride saline solution, and control the temperature at -10°C, and quickly pump the acetone solution of Florfenicol into the liquid surface of the saline solution through a high-pressure delivery pump, and the outlet pipe The flow velocity is greater than 3 m / s. Continue vigorous stirring for 60 min. A suspension of florfenicol was obtained. Wherein the volume ratio of the saline solution to the acetone solution of Florfenicol is 50:1.

[0033] (4) The suspension is subjected to solid-liquid separation, and the florfenicol superfine powder product can be obtained after drying. Th...

Embodiment 3

[0035] (1) In the reaction kettle, add solvent acetone, dissolve the former powder of Florfenicol in acetone, be mixed with the acetone solution of Florfenicol, wherein the concentration of Florfenicol is 50mg / ml.

[0036] (2) In another reactor, prepare calcium chloride brine solution, wherein the salt concentration is 30%.

[0037] (3) Turn on the strong stirring of the calcium chloride saline solution, control the temperature at -30°C, and quickly pump the acetone solution of Florfenicol into the liquid surface of the saline solution through a high-pressure delivery pump, and The flow velocity is greater than 3 m / s. Continue vigorous stirring for 60 min. A suspension of florfenicol was obtained. Wherein the volume ratio of the saline solution to the acetone solution of Florfenicol is 10:1.

[0038] (4) The suspension is subjected to solid-liquid separation, and the florfenicol superfine powder product can be obtained after drying. The obtained florfenicol superfine powd...

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Abstract

The invention discloses a preparation method of florfenicol superfine powder, which comprises adding solvent acetone into a reaction kettle, dissolving the original florfenicol powder in acetone, preparing florfenicol acetone solution, and preparing florfenicol acetone solution in another In a reaction kettle, a saline solution is prepared, and the saline solution is started to stir vigorously, and the acetone solution of florfenicol is quickly pumped into the saline solution through a high-pressure delivery pump. The present invention adopts a saline solution, especially a high-concentration saline solution close to a saturated state, which has a particularly excellent ultrafine effect, and at the same time, the acetone solution of Florfenicol is quickly pumped into the liquid surface of the saline solution through a high-pressure delivery pump Below, the fluid flow can be effectively controlled to be in a fully developed high-speed turbulent state, which is conducive to the realization of ultra-fine effects.

Description

technical field [0001] The invention belongs to the technical field of organic chemistry, and in particular relates to a preparation method of florfenicol superfine powder. Background technique [0002] Florfenicol (Florfenicol) Chinese name: fluprofen; [0003] It was first launched in Japan in 1990. In 1993, Norway approved the drug to treat salmon furunculosis. In 1995, France, the United Kingdom, Austria, Mexico and Spain approved it to treat bovine respiratory system bacterial diseases. In Japan and Mexico, it is also approved to be used as a feed additive for pigs to prevent and treat bacterial diseases in pigs. Our country has passed the approval of this drug at present. [0004] Florfenicol has the characteristics of broad antibacterial spectrum, good absorption, wide distribution in the body, safety and high efficiency, and has no potential aplastic anemia, teratogenic, carcinogenic and mutagenic effects, especially chloramphenicol has serious It is forbidden to b...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/14A61K31/165A61K47/02A61P31/04
CPCA61K9/143A61K31/165A61P31/04
Inventor 钟旭辉张治国周国朝雷飞飞
Owner 京山瑞生制药有限公司
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