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Artemisinin is a drug for multi-drug resistant strains of falciparum malaria. The compound (an sesquiterpene lactone) is isolated from the shrub Artemisia annua. Not all shrubs of this species contain artemisinin. Apparently it only is produced by the plant when the plant is subjected to certain conditions.
Chemically it is (3R,5aS,6R,8aS,9R,12S,12aR)-octahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10(3H)-one, C15H22O5.
History
Artemisia has been used by Chinese herbalists for more than a thousand years in the treatment of many illnesses, such as skin diseases and malaria. In the 1960s a research program was set up by the Chinese army to find an adequate treatment of malaria. In 1972, in the course of this research, Tu Youyou discovered artemsinin in the leaves of Artemisia annua. The drug is named qinghaosu in Chinese. It was one of many candidates then tested by Chinese scientists from a list of nearly 200 traditional Chinese medicines for treating malaria. It was the only one that was effective.
It remained largely unknown to the rest of the world for about 10 years, due to the Communist Chinese government at the time. The rest of the world finally found out about the drug from an article in a Chinese medical journal. People were sceptic at first, because the Chinese had made earlier statements about having found treatments of malaria before, but these were unsubstantiated. Another reason was the peroxide part of the molecule. It was thought unlikely this would be a stable molecule, and so would not last long enough to be effective. This turned out not to be the case.
The Chinese government at the time, however, was very wary of western scientists, and would not give anyone either the plant or the refined drug. People around the world now started looking for the shrub themselves, to see if they could find it. They finally found it along the Potomac river, in Washington, D.C. Apparently it was a very common shrub, found in many parts of the world. It took another 10 years of research before the drug was finally commercially available. By this time relations between Communist China and the rest of the world had improved, and scientific information could be exchanged.
The drug is these days used in China and Vietnam without much regard to taking precautions for maybe creating resistance of the malaria parasite to this drug as well.
Since that time, more potent derivatives have been developed from artemisinin, such as artemether and artesunate. However, their activity decreases after one to two hours. To counter this drawback, artemisinin is given alongside lumefantrine to treat uncomplicated falciparum malaria. Lumefantrine has a half-life of about 3 to 6 days. Such a treatment is called ACT (artemisinin-based combination therapy) such as: artemether-lumefantrine, artesunate-mefloquine, artesunate-amodiaquine, and artesunate-sulfadoxine/pyrimethamine.
Recent trials have shown that ACT is more than 90 % effective, with a recovery of malaria after three days, especially for the chloroquine-resistant Plasmodium falciparum.
The World Health Organisation has recommended that a switch to ACT should be made in all countries were the malaria parasite has developed a resistance to chloroquine. Artemisinin and its derivitives are now standard components of malaria treatment in China, Vietnam, and some other countries in Asia and Africa, where they have proved to be the best-ever anti-malarial drugs. They have minimal adverse side effects. Artemisinin is not currently available in the United States or Canada in large scale.
To counter the present shortage in leaves of Artemisia annua, researchers have been searching for a way to develop artemisinin artificially in the laboratory. The compound, called OZ-277, developed by Jonathan Vennerstrom in University of Nebraska has even proved to be more effective than the natural product in test-tube trials.
How it works
The compound has a peroxide group in its structure. When the it come into contact with high iron concentrations, the molecule becomes unstable and "explodes" into free radicals. High concentrations of iron are found in red blood cells, which is also where the malaria parasites are found. When the compound enters the red blood cell, it will release the free radicals, which are highly destructive to the parasites.
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