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Published bySade Allwood Modified over 9 years ago
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D3 Analgesics- pain killers Aspirin (acetylsalicylic acid) Methyl salicylate Paracetamol Ibuprofen Opiates
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Modes of action Mild pain killers (aspirin, paracetamol)- prevents the synthesisof a specific enzyme in the body. The enzyme cause fever and swelling. Strong pain killers (morphine)- interact with receptor sites in the brain so the pain signals are blocked
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Found in willow tree bark 1899 Bayer Company introduced the etanoate ”Aspirin” Which functional groups? Aspirin is less irritating for the stomach than salicylic acid Salicylic acid ethanoic ester-aspirin
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Aspirin, cont. Anti inflammatory- may be used for artritis and rheumatism Prevents blood clotting- prevents strokes and heart attacks Side effects include internal bleeding, ulceration Reye’s syndrome in children, a potentially fatal liver and brain disorder Too high dose may rise the pH in the blood- acidosis
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Salicylic acid methyl ester- methyl salicylate (oil of wintergreen) Has a characteristic smell Used in liniments to rub into the skin- antiinflammatory Which functional groups? Reaction mechanism?
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Paracetamol- acetaminophen Preferred for children- have less problematic side effects compared to aspirin May cause liver failure if ingested in high amounts Functional groups?
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Pro and contra for aspirin and paracetamol? Aspirin Paracetamol
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Ibuprofen, ipren For headaches- in Sweden and elswhere?
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Opiates Morphine, codeine and diamorphin (heroin) Interact with receptor sites in the brain so the pain signals are blocked Differences in functional groups? Can they be transferred into each other?
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Naturally occurring In opium- poppy seeds Morphine and codeine Also contain papaverin, fentanyl, oxymorphone, hydromorphone Opiates are used as painkillers, but are also highly addictive
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Synthesis of heroin from morphin
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Water solubility Which does most easily pass through cell membranes? morphine codeine heroine
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