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Quinine chemical structure
| (R)-(6-methoxyquinolin-4-yl)((2S,4S,8R)- 8-vinylquinuclidin-2-yl)methanol|
| CAS number |
| ATC code |
| PubChem |
| DrugBank |
|Molecular weight||324.417 g/mol|
|Bioavailability||76 to 88%|
|Metabolism||Hepatic (mostly CYP3A4 and CYP2C19-mediated)|
|Elimination half-life||~18 hours|
|Pregnancy category||C (USA), D (Au)|
|Routes of administration||Oral, intravenous|
Quinine (Template:IPA-en, Template:IPA-en) is a natural white crystalline alkaloid having antipyretic (fever-reducing), antimalarial, analgesic (painkilling), and anti-inflammatory properties and a bitter taste. It is a stereoisomer of quinidine.
The bark of the cinchona tree is used to make quinine. The medicinal properties of the cinchona tree were originally discovered by the Quechua Indians of Peru and Bolivia; later, the Jesuits were the first to bring the cinchona to Europe.
Quinine was the first effective treatment for malaria caused by Plasmodium falciparum, appearing in therapeutics in the 17th century. It remained the antimalarial drug of choice until the 1940s, when other drugs replaced it. Since then, many effective antimalarials have been introduced, although quinine is still used to treat the disease in certain critical situations. Quinine is available with a prescription in the United States and over-the-counter, in very small quantities, in tonic water. Quinine is also used to treat lupus, nocturnal leg cramps and arthritis.
Mechanism of action against P. falciparumEdit
As with other quinoline anti-malarial drugs, the action of quinine has not been fully resolved. The most widely accepted hypothesis of quinine action is based on the well-studied and closely related quinoline drug, chloroquine. This model involves the inhibition of hemozoin biocrystallization, which facilitates the aggregation of cytotoxic heme. Toxic free heme accumulates in the parasites, leading to their death.
Quinine is an effective muscle relaxant, long used by the Quechua Indians of Peru to halt shivering due to low temperatures. The Peruvians would mix the ground bark of cinchona trees with sweetened water to offset the bark's bitter taste, thus producing tonic water.
Quinine has been used in un-extracted form by Europeans since at least the early 1600s. Quinine was first used to treat malaria in Rome in 1631. During the 1600s, malaria was endemic to the swamps and marshes surrounding the city of Rome. Malaria was responsible for the death of several popes, many cardinals and countless common Roman citizens. Most of the priests trained in Rome had seen malaria victims and were familiar with the shivering brought on by the febrile phase of the disease. The Jesuit brother Agostino Salumbrino (1561-1642), an apothecary by training who lived in Lima, observed the Quechua using the bark of the cinchona tree for that purpose. While its effect in treating malaria (and hence malaria-induced shivering) was unrelated to its effect in controlling shivering from rigors, it was still a successful medicine for malaria. At the first opportunity, he sent a small quantity to Rome to test in treating malaria. In the years that followed, cinchona bark was known as Jesuit's bark and became one of the most valuable commodities shipped from Peru to Europe.
The form of quinine most effective in treating malaria was found by Charles Marie de La Condamine in 1737. Quinine was isolated and named in 1820 by French researchers Pierre Joseph Pelletier and Joseph Bienaimé Caventou. The name was derived from the original Quechua (Inca) word for the cinchona tree bark, "quina" or "quina-quina", which roughly means "bark of bark" or "holy bark". Prior to 1820, the bark was first dried, ground to a fine powder and then mixed into a liquid (commonly wine) which was then drunk. Large scale use of quinine as a prophylaxis started around 1850.
Quinine also played a significant role in the colonization of Africa by Europeans. The harbinger of modern pharmacology, quinine was the prime reason Africa ceased to be known as the white man's grave. A historian has stated that "it was quinine's efficacy that gave colonists fresh opportunities to swarm into the Gold Coast, Nigeria and other parts of west Africa".
To maintain their monopoly on cinchona bark, Peru and surrounding countries began outlawing the export of cinchona seeds and saplings beginning in the early 19th century. The Dutch government persisted in their attempts to smuggle the seeds, and by the 1930s Dutch plantations in Java were producing 22 million pounds of cinchona bark, or 97% of the world's quinine production. During World War II, Allied powers were cut off from their supply of quinine when the Germans conquered Holland and the Japanese controlled the Philippines and Indonesia. The United States, however, had managed to obtain four million cinchona seeds from the Philippines and begin operation of cinchona plantations in Costa Rica. It came too late, tens of thousands US troops in Africa and the South Pacific died due to the lack of quinine. Despite controlling the supply, the Japanese did not make effective use of quinine, and thousands of Japanese troops in the Southwest Pacific died as a result.
Cinchona trees remain the only practical source of quinine. However, under wartime pressure, research towards its synthetic production was undertaken. A formal chemical synthesis was accomplished in 1944 by American chemists Robert Burns Woodward and W.E. Doering. Since then, several more efficient quinine total syntheses have been achieved,
Dosing and indicationEdit
Quinine is a basic amine and is therefore always presented as a salt. Various preparations that exist include the hydrochloride, dihydrochloride, sulfate, bisulfate and gluconate. This makes quinine dosing complicated since each of the salts has a different weight.
The following amounts of each form are equal:
- quinine base 100 mg
- quinine bisulfate 169 mg
- quinine dihydrochloride 122 mg
- quinine hydrochloride 111 mg
- quinine sulfate (actually (quinine)2H2SO4∙2H2O) 121 mg
- quinine gluconate 160 mg.
All quinine salts may be given orally or intravenously (IV); quinine gluconate may also be given intramuscularly (IM) or rectally (PR). The main problem with the rectal route is that the dose can be expelled before it is completely absorbed; this can be corrected by giving a half dose again.
The IV dose of quinine is 8 mg/kg of quinine base every eight hours; the IM dose is 12.8 mg/kg of quinine base twice daily; the PR dose is 20 mg/kg of quinine base twice daily. Treatment should be given for seven days.
The preparations available in the UK are quinine sulfate (200 mg or 300 mg tablets) and quinine hydrochloride (300 mg/ml for injection). Quinine is not licensed for IM or PR use in the UK. The adult dose in the UK is 600 mg quinine dihydrochloride IV or 600 mg quinine sulfate orally every eight hours. For nocturnal leg cramps, the dosage is 200–300 mg at night.
In the United States, quinine sulfate is commercially available in 324-mg tablets under the brand name Qualaquin; the adult dose is two tablets every eight hours. There is no injectable preparation of quinine licensed in the U.S.: quinidine is used instead.
Quinine is not recommended for malaria prevention (prophylaxis) because of its side-effects and poor tolerability, not because it is ineffective. When used for prophylaxis, the dose of quinine sulfate is 300–324 mg once daily, starting one week prior to travel and continuing for four weeks after returning.
- See: cinchonism
It is usual for quinine in therapeutic doses to cause cinchonism; in rare cases, it may even cause death (usually by pulmonary edema). The development of mild cinchonism is not a reason for stopping or interrupting quinine therapy and the patient should be reassured. Blood glucose levels and electrolyte concentrations must be monitored when quinine is given by injection. The patient should ideally be in cardiac monitoring when the first quinine injection is given (these precautions are often unavailable in developing countries where malaria is endemic).
Cinchonism is much less common when quinine is given by mouth, but oral quinine is not well tolerated (quinine is exceedingly bitter and many patients will vomit after ingesting quinine tablets): Other drugs such as Fansidar (sulfadoxine (sulfonamide antibiotic) with pyrimethamine) or Malarone (proguanil with atovaquone) are often used when oral therapy is required. Quinine ethyl carbonate is tasteless and odourless, but is only commercially available in Japan. Blood glucose, electrolyte and cardiac monitoring are not necessary when quinine is given by mouth.
Quinine can cause paralysis if accidentally injected into a nerve. It is extremely toxic in overdose, and the advice of a poisons specialist should be sought immediately.
Quinine in some cases can lead to constipation, erectile dysfunction and diarrhea.
Despite popular belief, quinine is an ineffective abortifacient (in the US, quinine is listed as Pregnancy category C ). Pregnant women who take toxic doses of quinine will suffer from renal failure before experiencing any kind of quinine-induced abortion. Indeed, quinine is the only drug recommended by the WHO as firstline treatment for uncomplicated malaria in pregnancy.
Quinine can cause hemolysis in G6PD deficiency, but again this risk is small and the physician should not hesitate to use quinine in patients with G6PD deficiency when there is no alternative. Quinine can also cause drug-induced immune thrombocytopenic purpura (ITP).
Some studies have related the use of quinine and hearing impairment, in particular high-frequency loss, but it has not been conclusively established whether such impairment is temporary or permanent.
Regulation by the United States Food and Drug AdministrationEdit
From 1969 to 1992, the U.S. Food and Drug Administration (FDA) received 157 reports of health problems related to quinine use, including 23 which had resulted in death. In 1994, the FDA banned the use of over-the-counter (OTC) quinine as a treatment for nocturnal leg cramps. Pfizer Pharmaceuticals had been selling the brand name Legatrin for this purpose. Doctors may still prescribe quinine, but the FDA has ordered firms to stop marketing unapproved drug products containing quinine. The FDA is also cautioning consumers about off-label use of quinine to treat leg cramps. Quinine is approved for treatment of malaria, but is also commonly prescribed to treat leg cramps and similar conditions. Because malaria is life-threatening, the risks associated with quinine use are considered acceptable when used to treat that affliction.
Though Legatrin was banned by the FDA for the treatment of leg cramps, drug manufacturer URL Mutual has branded a quinine containing drug named "Qualaquin". Qualaquin is marketed as a treatment for malaria and is only sold in the United States by prescription. In 2004, the CDC reported only 1,347 confirmed cases of malaria in the United States.
Non-medical uses of quinineEdit
Quinine is a flavor component of tonic water and bitter lemon. According to tradition, the bitter taste of anti-malarial quinine tonic led British colonials in India to mix it with gin, thus creating the gin and tonic cocktail, which is still popular today in many parts of the world, especially the U.K., United States, Canada, parts of Australia and Lhasa, Tibet.
Quinine (and quinidine) are used as the chiral moiety for the ligands used in Sharpless asymmetric dihydroxylation.
In South Africa, quinine is an ingredient of a Clifton Instant Drink named Chikree produced by Tiger Food Brands.
- ↑ 1.0 1.1 1.2 Conner, Clifford D. (2005). A People's History of Science: Miners, Midwives, and 'Low Mechanicks', 95–96, New York: Nation Books. Also cites Porter, Roy (1998). The Greatest Benefit to Mankind: A Medical History of Humanity, 465–466, New York: W. W. Norton.
- ↑ Fire in the Sky; Willmott, Barrier and the Javelin.
- ↑ Woodward R, Doering W (1944). The Total Synthesis of Quinine. J Am Chem Soc 66 (849).
- ↑ Kaufman, Teodoro S., Rúveda, Edmundo A. (2005). Die Jagd auf Chinin: Etappenerfolge und Gesamtsiege. Angewandte Chemie, Int. Ed. 117 (6): 876–907.
- ↑ World Health Organization. [http:apps.who.int/malaria/docs/TreatmentGuidelines2006.pdf Guidelines for the treatment of malaria]. World Health Organization. URL accessed on 10 August 2009.
- ↑ Dorndorp A, Nosten F, Stepniewska K, et al. (2005). Artesunate verus quinine for treatment of severe falciparum malaria: a randomised trial. Lancet 366: 717–25.
- ↑ Reyburn H, Mtove G, Hendriksen I, von Seidlein L (2009). Oral quinine for the treatment of uncomplicated malaria. Brit J Med 339: b2066.
- ↑ Achan J, Tibenderana JK, Kyabayinze D, et al. (2009). Effectiveness of quinine versus artemether-lumefantrine for treating uncomplicated faciparum malaria in Ugandan children. Brit Med J 338.
- ↑ Barennes H, et al. (1996). Efficacy and pharmacokinetics of a new intrarectal quinine formulation in children with Plasmodium falciparum malaria. Brit J Clin Pharmacol 41 (5): 389.
- ↑ Barennes, H. (2006). Safety and efficacy of rectal compared with intramuscular quinine for the early treatment of moderately severe malaria in children: randomised clinical trial. Brit Med J 332 (7549): 1055–57.
- ↑ BNF 56: Nocturnal leg cramps Accessed 30/11/2008
- ↑ Center for Disease Control (1991). Treatment with Quinidine Gluconate of Persons with Severe Plasmodium falciparum Infection: Discontinuation of Parenteral Quinine. Morb Mort Weekly Rep 40 (RR-4): 21–23.
- ↑ Magill A, Panosian C (2005). Making Antimalarial Agents Available in the United States. New Engl J Med 353 (4): 335–337.
- ↑ Jamaludin A, Mohamad M, Navaratnam V, et al. (1988). Relative bioavailability of the hydrochloride, sulphate and ethyl carbonate salts of quinine. Br J Clin Pharmacol 25 (2): 261–3.
- ↑ Optically active isomers of quinine and quinidine and their respective biological action Accessed 26/1/2009
- ↑ Sanders, L."Poison Pill", "The New York Times", 4/13/2008.
- ↑ Dannenberg AL (1983). Use of quinine for self-induced abortion. The Southern Medical Journal 76 (7): 846–849.
- ↑ Yeka A, Achan J, D'Alessandro U, Talisuna AO (2009). Quinine monotherapy for treating uncomplicated malaria in the era of artemisinin-based combination therapy: an appropriate public health policy?. Lancet Infect Dis 9, (7): 448–452.
- ↑ Department of Clinical Pharmacology, Huddinge University Hospital, Sweden (1994). The concentration-effect relationship of quinine-induced hearing impairment. Clin Pharmacol Ther 55 (3): 317–323.
- ↑ FDA Orders Stop to Marketing Of Quinine for Night Leg Cramps. FDA Consumer Magazine. Food and Drug Administration. URL accessed on 2009-07-31.
- ↑ FDA Orders Unapproved Quinine Drugs from the Market and Cautions Consumers About Off-Label Use of Quinine to Treat Leg Cramps. United States Food and Drug Administration. URL accessed on 2009-07-31.
- ↑ Malaria Surveillance - United States, 2004. Center for Disease Control. URL accessed on 2009-11-22.
- ↑ Hobhouse, Henry (2004). Šest rostlin, které změnily svět (in Czech), 59, Prague: Akademie věd České republiky.
- ↑ Ballestero, Jimena A., et al. (2005). Effects of Quinine, Quinidine, and Chloroquine on α9α10 Nicotinic Cholinergic Receptors. Molecular Pharmacology 68 (3): 822–829.
- ↑ (http://www.reefculturemagazine.com.au/cryptocaryon.html): Porritt, M., Cryptocaryon irritans, Reef Culture Magazine, 1. Retrieved 9th Jul 2009
Additional reading Edit
- Wolff RS, Wirtschafter D, Adkinson C (June 1997). Ocular quinine toxicity treated with hyperbaric oxygen. Undersea Hyperb Med 24 (2): 131–4.
- Hobhouse, Henry - Seeds of Change Six Plants that Transformed Mankind C2005 ISBN(10) 1-59376-049-3
- Jesuits' Powder
- From intox databank
- From inchem
- Database file on Quinine from rain-tree.com
- Catalytic Asymmetric Synthesis of Quinine and Quinidine
- Summary article on history of Quinine in Chemical and Engineering News
- Quinine news page - Alcohol and Drugs History Society
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