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study of drug design to optimize PK,PD, pharmacology, and synthesis of new drug candidates |
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study and design of drug formulations for optimal delivery, stability, PK, and patient acceptance |
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study of biochemical and physiological effects of drugs on organisms |
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study of cellular and molecular interactions of drugs with their receptors |
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study of the factors that control or influence the concentration of drugs in various tissues or organs of the body |
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study of toxic effects of drugs and chemicals |
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study of inheritance of characteristics patterns of interaction between drugs and organisms to explain pharmacodynamics response |
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-IUPAC -common name -compound name -generic name -brand (trade) name |
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conc. drug in octanol/conc. drug in aq. buffer |
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physical/chemical properties |
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-melting/boiling pt -solubility -molecular weight/shape -acid/base properties -chemical reactivity/stability -molecular formula |
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water solubility, H bonding, and lipid solubility |
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plays an important role in acid/base properties and ionization |
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rate of extent of oral absorption is proportional to |
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-extent of ionization -aqueous solubility -lipid solubility -pH of stomach/small intestine |
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chemical reactivity/stability is important in terms of |
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chemical properties influence choice of |
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-dosage form -shelf live -drug-drug, drug-food incompatibilities |
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-natural -semi synthetic -synthetic |
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-pre 1930s -plants -animal tissues -bacteria/fungi |
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-extracts using aqueous organic solvents -mixtures of related and unrelated substances -pharmacognosy and natural products |
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study of medicinal drugs obtained from plants |
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diffcult in finding viable plant sources because of |
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-starting material from natural sources (analogs) -improved pharmacological effects -difficult functional groups -biotechnological-derived biomolecules |
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biotechnology-derived biomolecules |
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-isolated and identification of human gene DNA -use of DNA to synthesize proteins in vitro -modification of gene to improve properties of protein -modification to the protein itself by enzymes |
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-1940s-1980s -total synthesis from inexpensive starting materials -small molecule libraries from simple structural changes -control over structural features and properties -controversy over natural v. synthetic vitamins |
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controversy over natural v. synthetic vitamins |
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-same chemical ingredient -differ in degree of purity, inactive ingredients, by-products from 3rd world suppliers -interest in contamination of natural products with heavy metals, noxious weeds, manufacturing by products |
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