Raw material of veterinary medicine Sarafloxacin Hydrochloride Powder

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Sarafloxacin Hydrochloride Powder Usage and Synthesis.

Salafloxacin hydrochloride is a new animal-specific drug after enrofloxacin, developed and marketed by Abbott in the U.S. The antimicrobial activity of this product is stronger than that of difloxacin, norfloxacin, ofloxacin-butyl kanamycin and tobramycin, etc., and the antimicrobial activity of the anaerobic bacterial species is comparable to that of ciprofloxacin.

Uses and functions of Sarafloxacin Hydrochloride.

Sarafloxacin Hydrochloride is mainly used for the treatment of streptococcus and colibacillosis in swine, as well as bacterial infections such as E. coli and salmonella in poultry.

Sarafloxacin Hydrochloride is an animal-specific variety of the new antimicrobial drugs of fluoroquinolones, which has a significant killing effect on Gram-positive and negative bacteria.

It is mainly used in aquaculture to prevent and control fish diseases such as red head rotting gills and enteritis.

Pharmacological Effects of Sarafloxacin Hydrochloride.

Sarafloxacin Hydrochloride is a broad-spectrum antimicrobial with strong inhibitory effects against Escherichia coli, Salmonella, Pasteurella multocida, Proteus, Haemophilus, Pasteurella haemolytica, Staphylococcus (including penicillin-resistant beads), Streptococcus, Mycoplasma, etc., and the MIC90 (ug/ml) of the first three were 0.06, 0.06 and 0.015, and also has more antibacterial after-effects. Pharmacokinetics:The product is rapidly absorbed internally and by injection. Wide distribution in vivo, large apparent volume of distribution, high bioavailability for internal use, elimination half-life Indications:Antimicrobial. Extremely strong killing effect on Gram-positive and negative bacteria and mycoplasma.

Specificities of Bulk Sarafloxacin Hydrochloride Powder.

(1) Block DNA replication and act directly on the nucleus of bacteria.

(2) It interferes with the synthesis of DNA, thus killing the bacteria completely and preventing recurrence after stopping the drug.

(3) It is widely distributed and crosses the blood-brain barrier, so it has good therapeutic effects on respiratory diseases and cerebral colibacillosis, which are difficult to be cured by other drugs.

(4) It can be rapidly absorbed into the body, and the blood concentration can reach the peak in 1.5 hours after oral administration.

(5) It is well distributed in all tissues of the body.

(6) Because of rapid absorption and excretion, the residue of the drug is much lower than the prescribed amount after 6 hours of withdrawal after five days of continuous use.

(7) There is no need to take into account the discontinuation time of the product, not to mention the pre-slaughter discontinuation period.

(8) No cross-resistance with other drugs, and still very sensitive to strains that have developed resistance to antibiotics, sulfonamides and furans. (9) Good stability, very low toxicity and side effects, safe to use, inexpensive, low cost of treatment.

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