17. When drugs are absorbed into the body and then eliminated, a graph of concentration in the body vs. time will have the general shape shown at right. Using a drug with a slower elimination rate wil . Absorption 0.9 0.8 Elimination 0.7 0.6 the area 0.5 under the curve. 0.4 A. decrease 0.3 B. increase 0.2 C. not change 0.1 10 20 30 40 50 60 70 Time Concentration

17. When drugs are absorbed into the body and then eliminated, a graph of concentration in the body vs. time will have the general shape shown at right. Using a drug with a slower elimination rate wil . Absorption 0.9 0.8 Elimination 0.7 0.6 the area 0.5 under the curve. 0.4 A. decrease 0.3 B. increase 0.2 C. not change 0.1 10 20 30 40 50 60 70 Time Concentration

World of Chemistry, 3rd edition

3rd Edition

ISBN:9781133109655

Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Chapter17: Equilibrium

Section: Chapter Questions

Problem 61A

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Penicillin is hydrolyzed and thereby rendered inactive by penicillinase, an enzyme present in some resistant bacteria. The mass of this enzyme in Staphylococcus aureus is 29.6 kd. The amount of penicillin hydrolyzed in 1 minute in 10 ml solution containing 10–9 g of purified penicillinase was measured as a function of the concentration of penicillin. Assume that the concentration of penicillin does not change during the assay. [Penicillin] µM Amount hydrolyzed (nanomoles) 1 0.11 3 0.25 5 0.34 10 0.45 30 0.58 50 0.61 a) Plot V0 versus [S] and 1/V0 1/[S]. Does penicillinase appear to obey Michaelis-Menten kinetics? b) What is the value of KM? c) What is the value of Vmax? d) What is the turnover number of penicillinase under these conditions? (This is the question I need help…