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Eszopiclone
From Wikipedia, the free encyclopedia
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Eszopiclone
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| Systematic (IUPAC) name | |
| (5S)-6-(5-Chloro-2-pyridinyl)-7-oxo-
6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin -5-yl 4-methyl-1-piperazinecarboxylate |
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| Identifiers | |
| CAS number | |
| ATC code | N05 |
| PubChem | |
| DrugBank | |
| Chemical data | |
| Formula | C17H17ClN6O3 |
| Mol. mass | 388.808 g/mol |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Protein binding | 52-59% |
| Metabolism | Hepatic oxidation and demethylation (CYP3A4 and CYP2E1-mediated) |
| Half life | 6 hours |
| Excretion | Renal |
| Therapeutic considerations | |
| Pregnancy cat. |
C(US) |
| Legal status | |
| Routes | Oral |
Eszopiclone, marketed by Sepracor under the brand-name Lunesta, is a nonbenzodiazepine hypnotic agent (viz., a sedative) used as a treatment for insomnia. Eszopiclone is the active stereoisomer of zopiclone, and belongs to the class of drugs known as cyclopyrrones.
Its main selling point is that it is approved by the U.S. Food and Drug Administration for long-term use, unlike almost all other hypnotic sedatives, which are approved only for the relief of short-term (6-8 weeks) insomnia.
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Eszopiclone is a hypnotic with a chemical structure unrelated to benzodiazepines or other drugs with known hypnotic properties. It is an agonist for the same family of receptors as benzodiazepines, but selectively binds to the receptor subtype known as omega¹. It is believed that this selectivity is responsible for its strong hypnotic effects and lack of significant anxiolytic properties. [1]
The pharmacokinetics of eszopiclone have been investigated in healthy subjects (adult and elderly) and in patients with hepatic disease or renal disease. In healthy subjects, the pharmacokinetic profile was examined after single doses of up to 7.5 mg and after once-daily administration of 1, 3, and 6 mg for 7 days. Eszopiclone is rapidly absorbed, with a time to peak concentration (T-max) of approximately 1 hour and a terminal-phase elimination half-life (t½) of approximately 6 hours. In healthy adults, Lunesta does not accumulate with once-daily administration, and its exposure is dose-proportional over the range of 1 to 6 mg. In patients 65 years of age and older, there is a slight prolonged elimination of eszopiclone (t½ of approximately 9 hours). Therefore, in elderly patients the starting dose of Lunesta should be decreased to 1 mg and the dose should not exceed 2 mg.
Eszopiclone is rapidly absorbed following oral administration. Peak plasma concentrations are achieved within approximately 1 hour after oral administration. Eszopiclone is weakly bound to plasma protein (52-59%). The large free fraction suggests that eszopiclone disposition should not be affected by drug-drug interactions caused by protein binding. The blood-to-plasma ratio for eszopiclone is less than one, indicating no selective uptake by red blood cells.
Following oral administration, eszopiclone is extensively metabolized by oxidation and demethylation. The primary plasma metabolites are (S)-zopiclone-N-oxide and (S)-N-desmethyl zopiclone; the latter compound binds to GABA receptors with substantially lower potency than eszopiclone, and the former compound shows no significant binding to this receptor. In vitro studies have shown that CYP3A4 and CYP2E1 enzymes are involved in the metabolism of eszopiclone. Eszopiclone did not show any inhibitory potential on CYP450 1A2, 2A6, 2C9, 2C19, 2D6, 2E1, and 3A4 in cryopreserved human hepatocytes.
After oral administration, eszopiclone is eliminated with a mean t½ of approximately 6 hours. Up to 75% of an oral dose of racemic zopiclone is excreted in the urine, primarily as metabolites. A similar excretion profile would be expected for eszopiclone, the S-isomer of racemic zopiclone. Less than 10% of the orally administered eszopiclone dose is excreted in the urine as parent drug.
In healthy adults, administration of a 3 mg dose of eszopiclone after a high-fat meal resulted in no change in AUC, a reduction in mean Cmax of 21%, and delayed T-max by approximately 1 hour. The half-life remained unchanged, approximately 6 hours. The effects of Lunesta on sleep onset may be reduced if it is taken with or immediately after a high-fat/heavy meal. Sepracor, the drug's manufacturer and developer, recommends against using eszopiclone immediately following a meal due to this interference.
Eszopiclone may take up to 7 to 10 days before sleep quality significantly improves.
Common side effects can include:
- unpleasant bitter or metallic taste/smell
- headaches
- cold-like symptoms
- pain
- daytime drowsiness
- lightheadedness
- dizziness
- loss of coordination
- upset stomach
- vomiting
- decreased sexual desire
- painful menstruation (periods)
- breast enlargement in males
- heartburn
- unusual dreams
Less common side effects can include:
- rashes
- itching
- chest pain
- swelling of the hands, feet, ankles, or lower legs
- painful or frequent urination
- bloody or cloudy urine
- back pain
If a person does not sleep immediately after taking their Eszopiclone (Lunesta) or if they get up shortly after taking their medication they may experience dizziness, lightheadedness, hallucinations (seeing things or hearing voices that are not there), as well as experience problems with coordination and memory.
If a person has taken Eszopiclone for longer than 1 - 2 weeks they should not stop taking the medication abruptly and should consult their doctor. Usually doctors will direct a slow reduction in dosage to minimise withdrawal symptoms. Particularly after abrupt cessation of medication, withdrawal symptoms may include:
- anxiety
- unusual dreams
- stomach and muscle cramps
- upset stomach
- vomiting
- sweating
- shakiness
- insomnia
- seizures (rare)
- death by overdose (rare)
- National Institute of Health - Medline Plus - (Eszopiclone)
- Eszopiclone labeling text (PDF)
- Sepracor.com
- Lunesta.com