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P17B.7 Pharmacokinetics is the study of the rates of absorption and elimination of drugs by organisms. In most cases, elimination is slower than absorption and is a more important determinant of availability of a drug for binding to its target. A drug can be eliminated by many mechanisms, such as metabolism in the liver, intestine, or kidney followed by excretion of breakdown products through urine or faeces. As an example of pharmacokinetic analysis, consider the elimination of beta adrenergic blocking agents (beta blockers), which are used in the treatment of hypertension. After intravenous administration of a beta blocker, the blood plasma of a patient was analysed for remaining drug and the data are shown below, where c is the drug concentration measured at a time t after the injection. t/min 30 60 120 150 240 360 480 c/(ng cm) 152 699 622 413 292 60 24 (a) Is the decay of the concentration of the drug first- or second-order in the drug? (b) Calculate the rate constant and half-life of the process. Comment: An essential aspect of drug development is the optimization of the half-life of elimination, which needs to be long enough to allow the drug to find and act on its target organ but not so long that harmful side effects become important.

P17B.7 Pharmacokinetics is the study of the rates of absorption and elimination of drugs by organisms. In most cases, elimination is slower than absorption and is a more important determinant of availability of a drug for binding to its target. A drug can be eliminated by many mechanisms, such as metabolism in the liver, intestine, or kidney followed by excretion of breakdown products through urine or faeces. As an example of pharmacokinetic analysis, consider the elimination of beta adrenergic blocking agents (beta blockers), which are used in the treatment of hypertension. After intravenous administration of a beta blocker, the blood plasma of a patient was analysed for remaining drug and the data are shown below, where c is the drug concentration measured at a time t after the injection. t/min 30 60 120 150 240 360 480 c/(ng cm) 152 699 622 413 292 60 24 (a) Is the decay of the concentration of the drug first- or second-order in the drug? (b) Calculate the rate constant and half-life of the process. Comment: An essential aspect of drug development is the optimization of the half-life of elimination, which needs to be long enough to allow the drug to find and act on its target organ but not so long that harmful side effects become important.

Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
8th Edition
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:William L. Masterton, Cecile N. Hurley
Chapter23: Organic Polymers, Natural And Synthetic
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P17B.7 Pharmacokinetics is the study of the rates of absorption and elimination of drugs by organisms. In most cases, elimination is slower than absorption and is a more important determinant of availability of a drug for binding to its target. A drug can be eliminated by many mechanisms, such as metabolism in the liver, intestine, or kidney followed by excretion of breakdown products through urine or faeces. As an example of pharmacokinetic analysis, consider the elimination of beta adrenergic blocking agents (beta blockers), which are used in the treatment of hypertension. After intravenous administration of a beta blocker, the blood plasma of a patient was analysed for remaining drug and the data are shown below, where c is the drug concentration measured at a time t after the injection. t/min 30 60 120 150 240 360 480 c/(ng cm) 152 699 622 413 292 60 24 (a) Is the decay of the concentration of the drug first- or second-order in the drug? (b) Calculate the rate constant and half-life of the process. Comment: An essential aspect of drug development is the optimization of the half-life of elimination, which needs to be long enough to allow the drug to find and act on its target organ but not so long that harmful side effects become important.
Transcribed Image Text:P17B.7 Pharmacokinetics is the study of the rates of absorption and elimination of drugs by organisms. In most cases, elimination is slower than absorption and is a more important determinant of availability of a drug for binding to its target. A drug can be eliminated by many mechanisms, such as metabolism in the liver, intestine, or kidney followed by excretion of breakdown products through urine or faeces. As an example of pharmacokinetic analysis, consider the elimination of beta adrenergic blocking agents (beta blockers), which are used in the treatment of hypertension. After intravenous administration of a beta blocker, the blood plasma of a patient was analysed for remaining drug and the data are shown below, where c is the drug concentration measured at a time t after the injection. t/min 30 60 120 150 240 360 480 c/(ng cm) 152 699 622 413 292 60 24 (a) Is the decay of the concentration of the drug first- or second-order in the drug? (b) Calculate the rate constant and half-life of the process. Comment: An essential aspect of drug development is the optimization of the half-life of elimination, which needs to be long enough to allow the drug to find and act on its target organ but not so long that harmful side effects become important.
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