Compound Ceftiofur Hydrochloride injecta

A technology for ceftiofur hydrochloride and injection, applied in the field of medicine, can solve the problems of uneven content distribution, high viscosity, poor stability, etc., and achieve the effects of treating bacterial infection, rapid absorption, and uniform content

Inactive Publication Date: 2010-07-21
商丘爱己爱牧生物科技股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] In view of the above situation, in order to overcome the defects of the prior art, the object of the present invention is to provide a compound ceftio

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0011] Example 1

[0012] The present invention is made by weight percentage: ceftiofur hydrochloride 1%, sulbactam sodium 0.5%, polyethylene glycol-40093% and anhydrous ethanol 5.5%. First, polyethylene glycol-400 and cephalosporin hydrochloride Thiofu was mixed, stirred, dissolved, then added absolute ethanol, stirred evenly, added sulbactam sodium, stirred and dissolved; at 35°C, filter with a 0.2μm pore size filter membrane, and divide the filtrate into bottles , Gland, seal, and package to obtain the injection of the present invention.

Example Embodiment

[0013] Example 2

[0014] The present invention is made by weight percentage: ceftiofur hydrochloride 5%, sulbactam sodium 2.5%, polyethylene glycol -400,076.5% and absolute ethanol 16%. First, polyethylene glycol-400 and cephalosporin hydrochloride Thiofu was mixed, stirred, dissolved, then added absolute ethanol, stirred evenly, added sulbactam sodium, stirred and dissolved; at 30℃, filter with a 0.18 pore size microporous membrane, and the filtrate is divided into bottles, The injection solution of the present invention is obtained by pressing and sealing and packaging.

Example Embodiment

[0015] Example 3

[0016] The present invention is made by weight percentage: ceftiofur hydrochloride 10%, sulbactam sodium 5%, polyethylene glycol-40065% and absolute ethanol 20%. First, polyethylene glycol-400 and cephalosporin hydrochloride Thiofu was mixed, stirred, dissolved, then added absolute ethanol, stirred evenly, added sulbactam sodium, stirred, and dissolved; at 32°C, filter with a 0.16 pore filter membrane, and divide the filtrate into bottles. The injection solution of the present invention is obtained by pressing and sealing and packaging.

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Abstract

The invention relates to compound Ceftiofur Hydrochloride injecta, which effectively solves the problems of local pain and the like caused by uneven content distribution, poor stability, large viscosity. The technical scheme adopted by the invention is as follows: the injecta is prepared from the following components by weight percent: 1-15% of Ceftiofur Hydrochloride, 0.5-7.5% of Sulbactam Sodium, 48-93% of polyethylene glycol and 5-50% of absolute ethyl alcohol, wherein the total amount is 100%; firstly the polyethylene glycol and the Ceftiofur Hydrochloride are mixed, stirred and dissolved, the absolute ethyl alcohol is added and evenly stirred, and the Sulbactam Sodium is added, stirred and dissolved; and a microfiltration membrane is used to filter under the temperature of 30-45 DEG C, the filtrate is subpackged in bottles, and the bottles are gladded, sealed and packed to obtain the injecta of the invention. The invention overcomes the defects of easy delamination and inconvenient use of Ceftiofur suspension injecta in the market, and provides the injecta with stability, even content and rapid absorption; and the compound Ceftiofur Hydrochloride injecta also can effectively cure bacterial infection producing extended-spectrum beta-lactamase (ESBL).

Description

1. Technical field [0001] The invention relates to the field of medicine, in particular to a compound ceftiofur hydrochloride injection. 2. Background technology [0002] Ceftiofur, also known as Ceftiofur, is the first animal-specific cephalosporin antibiotic created by Pharmacia Upjohn in the United States. Since it was approved by the FDA in 1988 for the treatment of respiratory infections in cattle, it has been widely used in veterinary clinics at home and abroad because of its excellent antibacterial activity and dynamic process in vivo. [0003] The mechanism of action of ceftiofur is the same as that of other β-lactam drugs. It can bind to bacterial receptor binding proteins (PBPs), inhibit transpeptidase, carboxypeptidase, and endopeptidase synthesized by bacterial cell walls, and prevent peptide chain crossover. The connection is prolonged, destroying the synthesis of bacterial cell walls, and achieving rapid and efficient bactericidal effect during the breeding pe...

Claims

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Application Information

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IPC IPC(8): A61K31/546A61K31/43A61K9/08A61P31/04
Inventor 赵永星杜向党连明香陈五常
Owner 商丘爱己爱牧生物科技股份有限公司
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