Difference between revisions of "Chloramphenicol"

Revision as of 13:54, 24 October 2008

The 3D Structure of Chloramphenicol

Chloramphenicol orginates from cultures of Streptomyces and was one of the first antibiotics to be synthetically mass-produced. It is a dichloracetic acid derivative. It's analogues florfenicol and thiamphenicol are discussed at the bottom of the page.

Mechanism of Action

Spectrum of Activity

Pharmacokinetic Considerations

Chloramphenicol and analogues: Highly lipophilic neutral small molecules. • Orally active. • Very wide volume of distribution – penetrates across cell membranes readily – the data shown on the slide are for penetration into bronchial secretions.

Bronchial fluid is a transcellular fluid – what are the barriers for a drug to diffuse into this fluid?

• Hepatic metabolism (varies between species and with age) for chloramphenicol. • A higher proportion of the administered dose of thiamphenicol and florphenicol are excreted unchanged in the urine.

Side Effects and Contraindications

Florfenicol and Thiamphenicol

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 [[Image: Chloramphenicol.png|thumb|right|250px|The 3D Structure of Chloramphenicol]]
-==Introduction==
-Chloramphenicol orginates from cultures of ''Streptomyces'' and was one of the first antibiotics to be synthetically mass-produced. It is a dichloracetic acid derivative. Its analogues florfenicol and thiamphenicol are discussed at the bottom of the page.
+Chloramphenicol orginates from cultures of ''Streptomyces'' and was one of the first antibiotics to be synthetically mass-produced. It is a dichloracetic acid derivative. It's analogues florfenicol and thiamphenicol are discussed at the bottom of the page.
 ==Mechanism of Action==
-Chloramphenicol works by inhibiting the transpeptidation of the peptide chain, during protein synthesis on the ribosomes. This will limit the growth and replication of bacteria but will not kill the bacteria so is a '''bacteriostatic''' antibiotic.
 ==Spectrum of Activity==
-*It is a broad spectrum antibiotic active against most gram-positives, many gram-negatives and all anaerobes. It is also active against rickettsia and chlamydophilia.
-*''Pseudomonas'' and mycobacteria species are resistant.
 ==Pharmacokinetic Considerations==
-They are very lipophilic neutral small molecules, which are orally active and have a very wide volume of distribution. It is thus capable of penetrating cell membranes and will enter the CSF. It is eliminated in the liver via hepatic metabolism with only 10% being excreted in the urine unchanged. The half-life varies between each species and also with age of the animal.
+Chloramphenicol and analogues: Highly lipophilic neutral small molecules.
+•	Orally active.
+•	Very wide volume of distribution – penetrates across cell membranes readily – the data shown on the slide are for penetration into bronchial secretions.
+Bronchial fluid is a transcellular fluid – what are the barriers for a drug to diffuse into this fluid?
+•	Hepatic metabolism (varies between species and with age) for chloramphenicol.
+•	A higher proportion of the administered dose of thiamphenicol and florphenicol are excreted unchanged in the urine.
 ==Side Effects and Contraindications==
-* A reversible suppression of haematopoiesis occurs in cats when recieving high doses. It's use in cats should be limited to seven days.
-* Myocardial depression has been noticed following intravenous administration.
-* If it is given per os, dogs and cats often have gastrointestinal irritation.
-* In man a fatal aplastic anaemia can occur, this has had severe implications on the veterinary world. In the EU it is now '''banned in all food producing animals in all of its forms''' (ie has no safe withdrawal period) to ensure it doesn't enter the food chain. The only licensed veterinary products are currently topical eye medication and off-shelf use of human oral and parenteral products in non-food producing animals.
 ==Florfenicol and Thiamphenicol==
-These are both analogues of chloramphenicol with similar antibacterial activity. With these a higher percentage of drug is excreted unchanged in the urine.
-More importantly they aren't associated with aplastic anaemia in man and so are authorised to be used in food-producing animals.
-[[Category:WikiDrugs]]