A single dose of a newly developed and approved drug is administered to a patient, and its concentration C in the blood is monitored. Since distribution in the blood is very fast, the drug can be assumed to be well mixed at any instant. At the initial time, C = 10 mg/L. The total rate of elimination of the drug from the blood is given by kCV, where V = volume of the blood [L] and k = elimination rate constant [h-1]. a) After 10 h, the drug concentration is found to have dropped to 2 mg/L
A single dose of a newly developed and approved drug is administered to a patient, and its concentration C in the blood is monitored. Since distribution in the blood is very fast, the drug can be assumed to be well mixed at any instant. At the initial time, C = 10 mg/L. The total rate of elimination of the drug from the blood is given by kCV, where V = volume of the blood [L] and k = elimination rate constant [h-1]. a) After 10 h, the drug concentration is found to have dropped to 2 mg/L
Introduction to Chemical Engineering Thermodynamics
8th Edition
ISBN:9781259696527
Author:J.M. Smith Termodinamica en ingenieria quimica, Hendrick C Van Ness, Michael Abbott, Mark Swihart
Publisher:J.M. Smith Termodinamica en ingenieria quimica, Hendrick C Van Ness, Michael Abbott, Mark Swihart
Chapter1: Introduction
Section: Chapter Questions
Problem 1.1P
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A single dose of a newly developed and approved drug is administered to a patient, and its
concentration C in the blood is monitored. Since distribution in the blood is very fast, the
drug can be assumed to be well mixed at any instant. At the initial time, C = 10 mg/L. The
total rate of elimination of the drug from the blood is given by kCV, where V = volume of
the blood [L] and k = elimination rate constant [h-1].
a) After 10 h, the drug concentration is found to have dropped to 2 mg/L, determine the
value of k
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