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'''Lymecycline''' is a [[tetracycline antibiotics|tetracycline]] [[broad-spectrum antibiotic]] marketed by the pharmeceutical company Galderma[http://www.galderma.com]. It is approximately 5000 times more [[soluble]] than [[tetracycline]] base and is unique amongst tetracyclines in that it is [[Absorption (chemistry)|absorbed]] by the "active transport" process across the intestinal wall, making use of the same  fast and efficient mechanism by which [[carbohydrate]]s are absorbed.{{ref|NZdrugdata}}
'''Lymecycline''' is a [[tetracycline antibiotics|tetracycline]] [[broad-spectrum antibiotic]] marketed by the pharmeceutical company Galderma[http://www.galderma.com]. It is approximately 5000 times more [[soluble]] than [[tetracycline]] base and is unique amongst tetracyclines in that it is [[Absorption (chemistry)|absorbed]] by the "active transport" process across the intestinal wall, making use of the same  fast and efficient mechanism by which [[carbohydrate]]s are absorbed.{{ref|NZdrugdata}}
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[[Category:Tetracycline antibiotics]]
[[Category:Tetracycline antibiotics]]


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[[es:Limeciclina]]
[[es:Limeciclina]]

Latest revision as of 17:03, 9 August 2012

Lymecycline
Clinical data
Pregnancy
category
Routes of
administration
oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability100% (oral)
Metabolism?
Elimination half-life?
Excretionrenal
Identifiers
CAS Number
PubChem CID
DrugBank
E number{{#property:P628}}
ECHA InfoCard{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
FormulaCH23N2O8
Molar mass478.879

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Lymecycline is a tetracycline broad-spectrum antibiotic marketed by the pharmeceutical company Galderma[1]. It is approximately 5000 times more soluble than tetracycline base and is unique amongst tetracyclines in that it is absorbed by the "active transport" process across the intestinal wall, making use of the same fast and efficient mechanism by which carbohydrates are absorbed.[2]

The greater absorption of Lymecycline allows for lower dosages to be used; the standard dose of 408 mg is equivalent to 300 mg tetracycline base, and in its action to 500 mg tetracycline hydrochloride. Lymecycline, unlike tetracycline hydrochloride, is soluble at all physiological pH values.

History

Lymecycline was released onto the pharmaceutical market in 1963.

Indications

Lymecycline, like other Tetracyclines, is used to treat a range of infections (see Tetracycline antibiotics group). Its better absorption profile makes it preferable to tetracycline for moderately severe acne and typically prescribed for 8 weeks at a time, but alternatives should be sought if no improvement occurs by 3 months.[3]

Dosage

The standard dose is 408mg (one capsule) twelve hourly by mouth. In particularly severe infections this dose may be increased to 1.224-1.632mg (three or four capsules) daily.

The 408mg once daily dosage for acne aids good drug compliance.

Lymecycline capsules

Formulation

Capsules containing 408mg of Lymecycline (brand name Tetrlysal 300).

References

  1. ^ New Zealand Datasheet August 2003
  2. ^ British National Formulary 45 March 2003

See also

Timeline of antibiotics

hu:Limeciklin th:ไลมีซัยคลิน

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