Tigecycline is indicated for the treatment of complicated skin and soft tissue, and intra-abdominal infections.
Tigecycline is a glycylcycline
Tigecycline has a broad-spectrum activity against multidrug-resistant gram-positive pathogens, some gram-negative organisms, and anaerobic organisms
Tigecycline exhibits bacteriostatic action by reversibly binding to the 30S ribosomal subunit and inhibiting protein translation.
Tigecycline does not undergo significant liver metabolism, but it is primarily eliminated via biliary/fecal excretion
Tigecycline is given via 30- to 60-minute IV infusion every 12 hours
Tigecycline is associated with nausea, vomiting, photosensitivity, pseudotumor cerebri, discolouration of permanent teeth when used during tooth development, and teratogenicity.
Glycylcyclines are modified tetracyclines with an extra dimethylglycylamido side chain.
Administration of tetracyclines is usually topical, or peroral, but tigecycline is IV only.
If used perorally, tetracyclines should not be taken with food because they readily bind with magnesium, iron, aluminium, and calcium, and the resulting molecule is then unable to be absorbed.
tetracyclines are not given to patients on iron and calcium supplements, as well as antacids, which can contain aluminium salts.
Tetracyclines are broad spectrum, meaning they can target a wide variety of Gram positive and negative bacteria.
Tetracyclines are used to treat severe acne or community acquired pneumonia.
Tetracyclines treat intracellular pathogens, such as mycoplasma pneumoniae which causes atypical, or walking pneumonia, and Chlamydia trachomatis which causes chlamydia.
Both doxycycline and tigecycline are also effective against MRSA
Tetracyclines are contraindicated in pregnant or breastfeedingwomen