Cefquinome  

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Cefquinome API

 

Haorui supplies high quality Cefquinome API produced by our GMP facility that has been successfully inspected by the FDA. We offer competitive prices and support our products with reliable technical and regulatory services.  Cefquinome API is available from R&D to commercial quantities. Please contact us for more details.

 

  The following information is provided for general information purposes ONLY.

 

What is Cefquinome?

Cefquinome (4GC) is a fourth generation cephalosporin with pharmacological and antibacterial properties valuable in the treatment of coliform mastitis and other infections. It is used in the treatment of both humans and animals. According to the Washington Post, it is used as a last line of defence to keep humans alive.
 
Properties of Cefquinome
Cefquinome is resistant to beta-lactamase. Chemically, its zwitterionic structure can facilitate rapid penetration across biological membranes, including porins of bacterial cell wall. Plus, it has a higher affinity to target penicillin binding proteins. Besides zwitterionic, it is also made of beta-lactam nucleus, quaternary ammonium, and aminothiazolyl moiety.

Cefquinome acts by inhibition of the cell wall synthesis, but it has a relatively short half-life of about two and half hours. It is less than 5% protein bound and is excreted unchanged in the urine.
 
Intervet
Intervet developed cefquinome to treat bovine respiratory disease, the most common disease in cattle. An injection, containing 25mg cefquinome per ml, is given to cattle and pigs.
 
Treatment
In cattle, the injection should help against respiratory disease caused by Mannheimia haemolytica and Pasteurella multocida. It also helps with acute E. coli mastitis, dermatitis, infectious ulbar necrosis, and interdigital necrobacillosis (which is foul in the foot). In calves, it is E. coli septicaemia.

For pigs, it would treat the bacterial infections of the lungs and respiratory tract caused by P. multocida, Haemophilus parasuis, Actinobacillus pleuropneumoniae, and Streptococcus suis. Mastitis-Metritis-Agalactia Syndrom (MMA) involved with E. coli, Staphylococcus, Streptococcus, and other cefquinome-sensitive organisms will also be treated. In piglets, the mortality rate in cases of meningitis caused by Streptococcus suis is reduced. It is used in the treatment of mild or moderate lesions caused by Staphylococcus hyicus and arthritis caused by Streptococcus and E. coli.
 
Usage
Shake the vial well before using.

Swab the septum before removing each dose. Use a dry sterile needle and syringe. An appropriately graduated syringe must be used to allow accurate administration of the required dose volume. This is particularly important when injecting small volumes, for example when treating piglets. The cap may be safely punctured up to 25 times. The 50 ml vial should be used for treating small piglets. When treating groups of animals, use a draw-off needle.
 
Caution/Warnings
These are some factors to be aware of before treating.

This product should not be used in animals known to be hypersensitive to ¦Â-lactam antibiotics.
Should not be administer to animals with a bodyweight less than 1.25kg.
Use of the product may result in localised tissue reaction. Tissue lesions are repaired by 15 days after the last administration of the product.
Hypersensitivity reactions to cephalosporins occur rarely.
The product does not contain an antimicrobial preservative.
To prevent the claimed infections in piglets, attention should be paid to hygiene and ventilation, and overcrowding should be avoided. When the first piglets are affected, careful examination of all animals in the same pen is recommended to enable an early treatment of any other infected piglets.
 
Human Use
The only 4GC approved in US for human use is Maxipime (cefepime HCI). There are two main reasons for cefepime¡¯s primary use in human medicine. For one, cefepime is the only agent approved for empiric monotherapy for neutropenic fever. The other reason is that cefepime is used to treat enteric pathogens of non-food-borne-disease.
 
Veterinary Medicine
Conditions of use are limited to therapeutic, parenteral, and individual animal use. Individual parental therapy of bovine respiratory disease data on cefquinome-related residues demonstrate that only very small amounts are present in the intestinal tract of treated cattle with gastro-intestinal activation.

However, treatment should be short, meaning a single injection daily for about a week. Treatment should only be given by prescription. Cefquinome should not be used in feeding and water.

Since 1994, in Europe, it was allowed to treat cattle by prescription only. In 1999, swines were included. By 2005, horses were allowed as well.

In the United States, the situation is pending for treatment of bovine respiratory disease. Even so, this is only available by prescription.

Cefquinome are also used for other illnesses, such as ¡°shipping fever,¡± a pneumonia-like illness commonly found in cows

Disclaimer:

Information on this page is provided for general information purposes. You should not make a clinical treatment decision based on information contained in this page without consulting other references including the package insert of the drug, textbooks and where relevant, expert opinion. We cannot be held responsible for any errors you make in administering drugs mentioned on this page, nor for use of any erroneous information contained on this page.    

 

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