Purity Pharmaceutical Material Vancomycin Antibiotic Vancomycin Hcl Vancomycin
Product Description
| Product name: |
Vancomycin Powder |
| CAS: |
1404-90-6 |
| EINECS : |
215-772-6 |
| Appearance: |
White |
| Density: |
1.65 g/cm³ |
| Test method: |
HPLC |
| Purity: |
99% |
| Shelf life: |
2 years |
Vancomycin is a glycopeptide antibiotic used to treat bacterial infections. Vancomycin is a safe and effective antibiotic for the treatment of severe infections caused by methicillin-resistant Staphylococcus aureus, methicillin-resistant coagulase-negative Staphylococcus and Enterococcus, including sepsis, lung infection, skin and soft tissue infection. For nosocomial lung infections of methicillin-resistant Staphylococcus aureus, vancomycin is the drug of choice.
1. Kill bacteria by inhibiting the growth and reproduction of bacteria. This drug interferes with the synthesis of the cell wall by interfering with peptidoglycan, a key component in the structure of the bacterial cell wall, and inhibits the production of phospholipids and polypeptides in the cell wall.
2. Vancomycin is mainly used in the treatment of infections in four aspects: first, the treatment of drug-resistant bacterial infections; in addition, it is also used in the treatment of antibiotic-resistant pseudomembranous enteritis caused by Clostridium difficile.
3. Vancomycin can also be used to treat colitis and intestinal inflammation; Vancomycin is also often used to prevent infection when installing cardiac catheters, venous catheters and other devices. Vancomycin can be used alone or in combination.
4. It can inhibit the synthesis of bacterial cell walls, has a strong effect on Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, etc., and has a good effect on Bacillus difficile, Bacillus anthracis, and Bacillus diphtheria.
5. There is no cross-resistance to other antibiotics, and there are very few resistant strains. Mainly used for endocarditis, sepsis, pseudomembranous enteritis, etc.
6. The medicine is not absorbed by oral administration. It must be dissolved with water for injection before intravenous infusion, and the instillation time should not be less than 1 hour. Too fast intravenous infusion can cause skin reactions, and too high concentration can cause thrombophlebitis; intramuscular injection can cause severe pain, so intramuscular injection is not allowed; it has severe ototoxicity and nephrotoxicity, so it should only be used for short-term rescue.
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