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  2. First pass effect - Wikipedia

    en.wikipedia.org/wiki/First_pass_effect

    An example of a drug where first-pass metabolism is a complication and disadvantage is in the antiviral drug remdesivir. Remdesivir cannot be administered orally because the entire dose would be trapped in the liver with little achieving systemic circulation or reaching target organs and cells (for example, cells infected with SARS-CoV-2 ).

  3. Salicylate testing - Wikipedia

    en.wikipedia.org/wiki/Salicylate_testing

    One of the first in vitro tests for aspirin was through the Trinder reaction. Aqueous ferric chloride was added to a urine sample, and the formation of the iron complex turned the solution purple. [2] This test was not specific to acetylsalicylic acid but would occur in the presence of any phenol or enol.

  4. Sublingual administration - Wikipedia

    en.wikipedia.org/wiki/Sublingual_administration

    Furthermore, after absorption from the gastrointestinal tract, such drugs must pass to the liver, where they may be extensively altered; this is known as the first pass effect of drug metabolism. Due to the digestive activity of the stomach and intestines, the oral route is unsuitable for certain substances, such as salvinorin A .

  5. Aspirin - Wikipedia

    en.wikipedia.org/wiki/Aspirin

    By 1899, Bayer had dubbed this drug Aspirin and was selling it globally. [15]: 27 The word Aspirin was Bayer's brand name, rather than the generic name of the drug; however, Bayer's rights to the trademark were lost or sold in many countries. Aspirin's popularity grew over the first half of the 20th century leading to fierce competition with ...

  6. Bioavailability - Wikipedia

    en.wikipedia.org/wiki/Bioavailability

    Whether a drug is taken with or without food will also affect absorption, other drugs taken concurrently may alter absorption and first-pass metabolism, intestinal motility alters the dissolution of the drug and may affect the degree of chemical degradation of the drug by intestinal microflora.

  7. Enteric coating - Wikipedia

    en.wikipedia.org/wiki/Enteric_coating

    An enteric coating is a polymer barrier applied to oral medication that prevents its dissolution or disintegration in the gastric environment. [1] This helps by either protecting drugs from the acidity of the stomach, the stomach from the detrimental effects of the drug, or to release the drug after the stomach (usually in the upper tract of the intestine). [2]

  8. Route of administration - Wikipedia

    en.wikipedia.org/wiki/Route_of_administration

    Enteric coated tablets are designed to dissolve in the intestine, not the stomach, because the drug present in the tablet causes irritation in the stomach. Administering medication rectally. The rectal route is an effective route of administration for many medications, especially those used at the end of life.

  9. Mechanism of action of aspirin - Wikipedia

    en.wikipedia.org/wiki/Mechanism_of_action_of_aspirin

    Additionally, aspirin induces the formation of NO-radicals in the body, which have been shown in mice to have an independent mechanism of reducing inflammation. This reduces leukocyte adhesion, which is an important step in immune response to infection. There is currently insufficient evidence to show that aspirin helps to fight infection. [18]