Enrofloxacin nano-microemulsion solution for treating Mycoplasma synoviae disease in poultry

A technology of mycoplasma synovialum and nano-microemulsion, which is applied in the field of enrofloxacin nano-microemulsion solution, can solve the problems of high toxicity and side effects, uneven effect, time-consuming and labor-intensive problems, achieve high bioavailability and improve solubility , good therapeutic effect

Inactive Publication Date: 2020-04-24
天津佰力喜动物药业有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, commonly used enrofloxacin preparations mainly include solid granules, injections, etc., while ordinary injections have a short half-life and are eliminated rapidly in the body, requiring multiple administrations, which is time-consuming and laborious; the bioavailability of solid granules is low, which is not conducive to large-scale production. scale dosing
And because the preparations of many manufacturers do not have technology at all, so the same dosage, the clinical effect is uneven, the product quality is unstable, the bioavailability is not high, and the disadvantages such as large toxic and side effects

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] A kind of enrofloxacin nano microemulsion solution for the treatment of poultry mycoplasma synovial bursa disease, this nano microemulsion is prepared by following method:

[0022] S1, prepare raw materials, the parts by weight of raw materials used are: 10 parts of enrofloxacin, 5 parts of diacetyl monoglyceride, 15 parts of OP-10, 10 parts of 1,2 propylene glycol, 60 parts of phosphate aqueous solution;

[0023] S2, in the reaction device that thermometer and reflux condenser are equipped with, add described weight enrofloxacin, OP-10, 1,2 propanediol, enrofloxacin, OP-10, 1,2 propanediol are in 50~ Disperse in phosphate aqueous solution by stirring, ultrasonication or homogenization at 150°C to obtain an emulsion;

[0024] S3, the emulsion in step S2 is slowly added to diacetyl monoglyceride, nitrogen gas is used to drive oxygen for 25-35min, and a mixture of ammonium persulfate and dimethyl azobisisobutyrate is added;

[0025] S4. Externally cool the reaction in st...

Embodiment 2

[0027] A kind of enrofloxacin nano microemulsion solution for the treatment of poultry mycoplasma synovial bursa disease, this nano microemulsion is prepared by following method:

[0028] S1, prepare raw materials, the parts by weight of raw materials used are: 5 parts of enrofloxacin, 10 parts of diethyl malonate, 10 parts of Tween2010, 10 parts of 1,2 propylene glycol, 65 parts of phosphate aqueous solution;

[0029] S2. In the reaction device equipped with a thermometer and a reflux condenser, add the weight of enrofloxacin, Tween20, and 1,2 propylene glycol, and put enrofloxacin, Tween20, and 1,2 propylene glycol at a temperature of 50 to 150°C Disperse in phosphate aqueous solution by stirring, ultrasonication or homogenization to obtain emulsion;

[0030] S3, the emulsion in the step S2 is slowly added in the diethyl malonate, the oxygen is driven by nitrogen gas for 25-35min, and the mixture of ammonium persulfate and dimethyl azobisisobutyrate is added;

[0031] S4. E...

Embodiment 3

[0033] A kind of enrofloxacin nano microemulsion solution for the treatment of poultry mycoplasma synovial bursa disease, this nano microemulsion is prepared by following method:

[0034] S1, prepare raw materials, the parts by weight of raw materials used are: 15 parts of enrofloxacin, 15 parts of acetyl tributyl citrate, 805 parts of Tween, 5 parts of 1,2 propylene glycol, 60 parts of vanadate aqueous solution;

[0035] S2. In the reaction device equipped with a thermometer and a reflux condenser, add the weight of enrofloxacin, Tween80, and 1,2 propylene glycol, and place enrofloxacin, Tween80, and 1,2 propylene glycol at a temperature of 50 to 150°C Disperse in vanadate aqueous solution by stirring, ultrasonication or homogenization to obtain emulsion;

[0036] S3, the emulsion in step S2 is slowly added to acetyl tributyl citrate, nitrogen gas is used to drive oxygen for 25-35min, and a mixture of ammonium persulfate and dimethyl azobisisobutyrate is added;

[0037] S4. ...

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Abstract

The invention discloses an enrofloxacin nano-microemulsion solution for treating Mycoplasma synoviae disease in poultry. The nano-microemulsion is prepared by the following method: preparing raw materials including 5-15 parts by weight of enrofloxacin, 5-15 parts by weight of an oil phase, 5-20 parts by weight of a surfactant, 5-20 parts by weight of a cosurfactant, and 30-80 parts by weight of awater phase; adding enrofloxacin, the surfactant and the cosurfactant into a reaction device, and dispersing in a water phase through stirring, ultrasonic treatment or homogenization treatment to obtain an emulsion; slowly adding the emulsion into an oil phase, introducing nitrogen to expel oxygen, and adding a mixture of initiators; and carrying out external cooling and polymerization on the above reaction to obtain the enrofloxacin nano-microemulsion solution. The invention aims to provide an enrofloxacin nano-microemulsion solution for treating Mycoplasma synoviae disease in poultry. The process effect of adopting a nano-microemulsion preparation is more stable than the effect of a common oral solution, and the enrofloxacin nano-microemulsion solution shows a better therapeutic effect on Mycoplasma synoviae disease in poultry.

Description

technical field [0001] The invention relates to the technical field of veterinary preparations, in particular to an enrofloxacin nano-microemulsion solution for treating poultry mycoplasma synovialis disease. Background technique [0002] Enrofloxacin is a synthetic third-generation quinolone antibacterial drug, also known as ethyl ciprofloxacin, which was approved by FDA on October 4, 1996. It is a special quinolone antibacterial drug for livestock, poultry and aquatic products. It can bind to subunit A of bacterial DNA gyrase, thereby inhibiting the cutting and joining functions of the enzyme, preventing the replication of bacterial DNA, and exhibiting antibacterial effect. It has broad-spectrum antibacterial activity and strong permeability. This product is a broad-spectrum bactericidal drug, which has special effects on mycoplasma, strong killing effect on Gram-negative bacteria, and good antibacterial effect on Gram-positive bacteria. Function, good oral absorption, hi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/107A61K31/496A61K47/14A61K47/26A61K47/10A61K47/02A61P31/04
CPCA61K9/1075A61K31/496A61K47/14A61K47/26A61K47/10A61K47/02A61P31/04
Inventor 张健
Owner 天津佰力喜动物药业有限公司
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