cephalosporin


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Related to cephalosporin: cephalosporin C

cephalosporin

 [sef″ah-lo-spor´in]
any of a large group of broad-spectrum antibiotics from Acremonium (formerly Cephalosporium), a genus of soil-inhabiting fungi. Cephalosporins are similar in structure and antimicrobial action to penicillin. The cephalosporins have been classified by “generations” according to general features of antimicrobial activity, with successive generations having increasing activity against gram-negative organisms and decreasing activity against gram-positive organisms.

ceph·a·lo·spo·rin

(sef'ă-lō-spōr'in),
Antibiotic produced by a Cephalosporium, but after the antibiotic was discovered the name Cephalosporium was changed to Acremonium.

cephalosporin

(sĕf-ə-lə-spôr′ĭn)
n.
Any of various beta-lactam antibiotics, derived from the fungus Acremonium chrysogenum or made semisynthetically, used to treat a wide range of bacterial infections.

cephalosporin

Infectious disease Any of a family of broad-spectrum tetracyclic triterpene antibiotics derived from Cephalosporium spp, which are similar chemically and in mechanism of action to penicillin Indications Skin and soft tissue infections, RTIs, UTIs, STDs, meningitis, endocarditis, septicemia of unknown portal of entry, anaerobic infections, polymicrobial infections Pharmacokinetics Absorbed orally, excreted by the dustributed in tissues Adverse reactions Hypersensitivity, rash, serum sickness, acute tubular damage. See Fourth-generation cephalosporin.
Cephalosporin generations
1st
IV agents–Cephalothin, cephaloridine
2nd
Oral agents, which had a longer half-life
3rd
↑ antibacterial spectrum to include H influenzae, anaerobic bacteria, eg Bacteroides fragilis
4th
Not all authors use the term ; further; ↑ antibacterial spectrum to include Pseudomonas species<</dd>
.

ceph·a·lo·spo·rin

(sef'ă-lō-spōr'in)
Antibiotic produced by a Cephalosporium, but after the antibiotic was discovered the name Cephalosporium was changed to Acremonium.

cephalosporin

One of a range of antibiotics first obtained from a Cephalosporium fungus found in the sea near a sewage outflow. Their chemical structure is very similar to that of the penicillins and many semisynthetic forms have been developed. Their toxicity is low and they are effective against a wide range of organisms. Unfortunately, the spelling of cephalosporin drug names shows an apparently arbitrary distribution of ‘ceph’, ‘cep’ and ‘cef’, with a strong tendency to the latter, assisted by the recent requirement to adopt European nomenclature regulations.

antibiotic 

1. Pertaining to the ability to destroy or inhibit other living organisms.
2. A substance derived from a mould or bacterium, or produced synthetically, that destroys (bactericidal) or inhibits the growth (bacteriostatic) of other microorganisms and is thus used to treat infections. Some substances have a narrow spectrum of activity whereas others act against a wide range of both gram-positive and gram-negative organisms (broad-spectrum antibiotics). Antibiotics can be classified into several groups according to their mode of action on or within bacteria: (1) Drugs inhibiting bacterial cell wall synthesis, such as bacitracin, vancomycin and the β-lactams based agents (e.g. penicillin, cephalosporins (e.g. ceftazidime, ceftriaxone, cefuroxime). (2) Drugs affecting the bacterial cytoplasmic membrane, such as polymyxin B sulfate and gramicidin. (3) Drugs inhibiting bacterial protein synthesis, such as aminoglycosides (e.g. amikacin sulfate, framycetin sulfate, gentamicin, neomycin sulfate and tobramycin), tetracyclines, macrolides (e.g. erythromycin and azithromycin) and chloramphenicol. (4) Drugs inhibiting the intermediate metabolism of bacteria, such as sulfonamides (e.g. sulfacetamide sodium) and trimethoprim. (5) Drugs inhibiting bacterial DNA synthesis, such as nalixidic acid and fluoroquinolones (e.g. ciprofloxacin, levofloxacin, moxifloxacin, norfloxacin and ofloxacin). (6) Other antibiotics such as fusidic acid, the diamidines, such as propamidine isethionate and dibrompropamidine. Syn. antibacterial. See antiinflammatory drug; fusidic acid.

ceph·a·lo·spo·rin

(sef'ă-lō-spōr'in)
Antibiotic produced by a Cephalosporium.
References in periodicals archive ?
Cephalosporin Drugs are categorized together based on the category of bacteria against which they are most efficient.
The cephalosporin production is carried out by submerged fermentation and solid state fermentation (Kim et al., 2007; Cuadra et al., 2008).
We have not found any association between stage of liver disease and cephalosporin resistance in our study.
How Safe is It to Prescribe Cephalosporins in Patients with Infectious Mononucleosis?Implications for Clinical ENT Practice.
In vivo activity of a novel anti-methicillin-resistant Staphylococcus aureus, cephalosporin, ceftaroline, against vancomycin-susceptible and-resistant Enterococcus faecalis strains in a rabbit endocarditis model: a comparative study with linezolid and vancomycin.
* Despite nucleic acid amplification test (NAAT) being negative for Chlamydia trachomatis, dual treatment with a cephalosporin plus either azithromycin or doxycycline is recommended by ACOG to prevent resistance to cephalosporins.
Yvonne et al6 reported a cephalosporin resistant, ESBL producing Salmonella Typhi from the blood of an Iraqi woman in Germany.
Avycaz is a fixed-combination drug containing ceftazidime, a previously approved cephalosporin antibacterial drug, and avibactam, a new beta-lactamase inhibitor.
Her unit also worked on the chemical structure of the drug cephalosporin C, closely related to the penicillin family.
The cephalosporin antibiotics are most similar to the penicillins in both structure and mechanism of action.