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study of biochemical and physiological effects of drugs. relationship between the concentration at the receptor site and the response of the tissue to that drug. EX: liodcaine on heart muscle and the duration of the action potential of fibers. > receptor binding, post receptor effects, chemical interactions. |
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look at drug movement throughout body. Relationship between drug dose and drug blood level. Drug absorption, bioavailability, distribution, metabolsim, elimination. |
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Five pharmacological parameters for serum drug concentration |
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Drug liberation, absorption, distribution, metabolism, excretion. |
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SOME drugs is metabolized from the portal circulation reducing bio availability. fraction of drug that is absorbed and actually reaches the blood. Low bioavailability: quickly metabolized by liver, imeediately after being absorbed in the small intestine. |
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point at which the concentration of the drug is in equilibrium with the rate of dose adminstration and the rate of elimiation. |
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Oral dosing intervals give peaks and troughs in the dose response curve, while intravenous is constant. |
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Intravenous drugs model of elimination.. |
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biphasic/ two compartment with serum level rapidly falling in the first phase. Tissue vs blood/good tissues (profused). Ex: digixon. Lots can be accumulated in the tissues while target is fine. Oral route is uniformly distribution. One compartment. |
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Aminoglycoside antibiotics... why pay attention to it? |
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Highly toxic, must perform peak and trough measurements. Concentrates at the kidneys bro! Toxic can damage kidneys and hearing. |
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Rf values match with standards. Comparison to see what drugs it can contain. |
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whole blood (trace element tube blue) with AAS.It intereferes with heme synthesis by binding to ALA's sulhydrl group. Navy blue top for others. |
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