Lumefantrine: Difference between revisions

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'''Lumefantrine''' is an [[antimalarial drug]] used in combination with [[artemether]] for the treatment of acute uncomplicated [[malaria]]. It is part of a class of drugs known as [[antimalarials]], which are used to prevent and treat malaria. Lumefantrine works by killing the organisms that cause malaria.
{{Short description|An antimalarial drug used in combination therapies}}
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477002123
| image = Lumefantrine.svg
| image_size = 200px
| image_alt = Chemical structure of Lumefantrine
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== History ==
'''Lumefantrine''' is an [[antimalarial drug]] used in combination with [[artemether]] to treat [[malaria]]. It is part of the [[artemisinin-based combination therapies]] (ACTs) recommended by the [[World Health Organization]] for the treatment of uncomplicated [[Plasmodium falciparum]] malaria.


Lumefantrine was first synthesized in the 1970s by the [[Chinese Academy of Medical Sciences]] as part of a national research project in [[China]] known as "Project 523", which aimed to find new drugs for the treatment of malaria.
==Pharmacology==
Lumefantrine is a [[lipophilic]] compound that is poorly soluble in water. It is absorbed in the [[gastrointestinal tract]] and is metabolized in the [[liver]] by the [[cytochrome P450]] system, primarily by the enzyme [[CYP3A4]]. The drug has a long half-life, which helps in maintaining therapeutic levels in the blood for an extended period, thus aiding in the prevention of malaria recurrence.


== Medical uses ==
==Mechanism of Action==
Lumefantrine works by interfering with the [[haem]] polymerization process in the [[Plasmodium]] parasites. This process is crucial for the parasite's survival as it detoxifies the free haem released during the digestion of [[hemoglobin]]. By inhibiting this process, lumefantrine causes the accumulation of toxic haem, leading to the death of the parasite.


Lumefantrine is used in combination with artemether for the treatment of acute uncomplicated malaria caused by [[Plasmodium falciparum]]. The combination of these two drugs is known as [[artemether/lumefantrine]], and is sold under the brand name Coartem among others.
==Clinical Use==
Lumefantrine is used in combination with artemether, marketed under the brand name [[Coartem]]. This combination is effective against [[chloroquine-resistant]] strains of Plasmodium falciparum. The combination therapy is administered orally and is typically given over a three-day course.


== Side effects ==
==Side Effects==
Common side effects of lumefantrine include [[headache]], [[dizziness]], [[anorexia]], and [[nausea]]. Serious side effects are rare but may include [[allergic reactions]] and [[QT interval prolongation]], which can lead to [[arrhythmias]].


Common side effects of lumefantrine include headache, dizziness, loss of appetite, and palpitations. In rare cases, it can cause severe skin reactions, liver problems, and changes in heart rhythm.
==History==
 
Lumefantrine was developed in the 1980s and was initially used in China. It gained international recognition after being included in the [[World Health Organization's List of Essential Medicines]]. The combination with artemether was developed to enhance efficacy and reduce the risk of resistance.
== Mechanism of action ==
 
Lumefantrine is thought to work by interfering with the digestion of [[haemoglobin]] by the malaria parasite. It is believed to inhibit the formation of [[beta-haematin]] by forming a complex with [[haemin]], a substance produced by the parasite as it digests haemoglobin.
 
== Pharmacokinetics ==
 
Lumefantrine is administered orally and is absorbed from the gastrointestinal tract. It is extensively metabolized in the liver by the [[cytochrome P450]] system, and its elimination half-life is approximately 4-5 days.
 
== See also ==


==Related pages==
* [[Artemether]]
* [[Malaria]]
* [[Antimalarial medication]]
* [[Antimalarial medication]]
* [[Artemisinin]]
* [[World Health Organization]]
* [[Malaria]]


[[Category:Antimalarials]]
[[Category:Antimalarial agents]]
[[Category:World Health Organization essential medicines]]
[[Category:World Health Organization essential medicines]]
[[Category:Drugs]]
{{Pharma-stub}}
{{Medicine-stub}}

Revision as of 10:40, 15 February 2025

Lumefantrine
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Lumefantrine is an antimalarial drug used in combination with artemether to treat malaria. It is part of the artemisinin-based combination therapies (ACTs) recommended by the World Health Organization for the treatment of uncomplicated Plasmodium falciparum malaria.

Pharmacology

Lumefantrine is a lipophilic compound that is poorly soluble in water. It is absorbed in the gastrointestinal tract and is metabolized in the liver by the cytochrome P450 system, primarily by the enzyme CYP3A4. The drug has a long half-life, which helps in maintaining therapeutic levels in the blood for an extended period, thus aiding in the prevention of malaria recurrence.

Mechanism of Action

Lumefantrine works by interfering with the haem polymerization process in the Plasmodium parasites. This process is crucial for the parasite's survival as it detoxifies the free haem released during the digestion of hemoglobin. By inhibiting this process, lumefantrine causes the accumulation of toxic haem, leading to the death of the parasite.

Clinical Use

Lumefantrine is used in combination with artemether, marketed under the brand name Coartem. This combination is effective against chloroquine-resistant strains of Plasmodium falciparum. The combination therapy is administered orally and is typically given over a three-day course.

Side Effects

Common side effects of lumefantrine include headache, dizziness, anorexia, and nausea. Serious side effects are rare but may include allergic reactions and QT interval prolongation, which can lead to arrhythmias.

History

Lumefantrine was developed in the 1980s and was initially used in China. It gained international recognition after being included in the World Health Organization's List of Essential Medicines. The combination with artemether was developed to enhance efficacy and reduce the risk of resistance.

Related pages