Ibuprofen belongs to a class of drugs called non-steroidal anti-inflammatory drugs (NSAIDs). Ibuprofen is a member of the non-steroidal anti-inflammatory drug (NSAIDs) family. NSAIDs reduce inflammation (swelling), pain, and temperature. Ibuprofen is used to treat mild to moderate pain, fever, osteoarthritis, rheumatoid arthritis, primary dysmenorrhea, and other conditions. Other members of this class include naproxen (Aleve), indomethacin (Indocin), nabumetone (Relafen) and several others. These drugs are used for the management of mild to moderate pain, fever, and inflammation. Prostaglandins are chemicals that are made by the body and are responsible for causing pain, fever and inflammation. Ibuprofen blocks the enzyme that makes prostaglandins (cyclooxygenase), resulting in lower levels of prostaglandins. As a consequence, inflammation, pain and fever are reduced.
Ibuprofen is a nonsteroidal anti-inflammatory drug that is used to treat symptoms caused by arthritis, such as swelling, pain, and stiffness. Ibuprofen is used mainly for the relief of headaches. It is also used to combat muscle aches, menstrual pain, aches from various illnesses (including the common cold and influenza), and post-surgical pains.
Ibuprofen is also often used to reduce fever (anti-pyretic), and many people take it as a painkiller (analgesic), although it has not been demonstrated to have remarkable effects on headaches. As with aspirin and paracetomol, two other pain-killing pharmaceuticals, ibuprofen features a six-membered ring structure, which avoids the polar environment of water. In addition, a comparatively small appended group of atoms can assist the drug in bonding to part of the receptor molecule, usually one of the prostaglandins. Prostaglandins are a class of biochemicals that cause inflammation of tissues, leading to pain. Unlike acetaminophen with three polar groups, ibuprofen only has one polar group, the carboxylic acid functional group, making this over-the-counter painkiller somewhat soluble in water and soluble in organic solvents.
To an organic chemist, ibuprofen is a white powder known also as (+/-)-2-(p-isobutylphenyl) propionic acid and has a molecular weight of 206.29, a melting point of about 76 degrees Celsius, and two isomers (R and S). Unlike its predecessor aspirin, ibuprofen is not as likely to create serious gastrointestinal side effects, such as stomach ulcers and internal bleeding. As a peripherally acting analgesic, ibuprofen does not appear to affect any opiate receptors in the brain and has a plasma half-life of 2.2 hours. When filtered by the kidneys and excreted in the urine, approximately 15 percent is unchanged drug, and between 50 and 60 percent are metabolites of ibuprofen. Asthmatic patients must use caution before taking ibuprofen, because of a potential for anaphylactic shock and potentially fatal bronchiospasms. Also, because ibuprofen and the other antipyretic and anti-inflammatory over-the-counter medications treat the symptoms of fever and inflammation, taking these drugs before seeing a physician may mask important diagnostic clues. For some users of ibuprofen, elevated liver enzyme activity (up to 15 percent greater) may suggest liver dysfunction that is only an artifact of the painkiller therapy.