/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 2 If a drug exhibits first-order e... [FREE SOLUTION] | 91影视

91影视

Log out

Learning Materials

Features

Discover

Chapter 2: Problem 2

If a drug exhibits first-order elimination, then (A) the elimination half-life is proportional to the plasma drug concentration. (B) the drug is eliminated at a constant rate. (C) hepatic drug metabolizing enzymes are saturated. (D) drug clearance will increase if the plasma drug concentration increases. (E) the rate of drug elimination \((\mathrm{mg} / \mathrm{min})\) is proportional to the plasma drug concentration.

Short Answer

Expert verified
The correct answer is (E).

Step by step solution

01

Understanding First-order Elimination

First-order elimination refers to the process where the rate of elimination of a drug is directly proportional to its concentration in the plasma. This means as the drug concentration changes, the rate of elimination changes proportionally.
02

Analyzing Option (A)

Option (A) states that the elimination half-life is proportional to the plasma drug concentration. This is incorrect for first-order kinetics, as the half-life is constant and does not depend on the concentration of the drug.
03

Analyzing Option (B)

Option (B) claims that the drug is eliminated at a constant rate. In first-order kinetics, elimination rate is not constant but changes with drug concentration, making this option incorrect.
04

Analyzing Option (C)

Option (C) suggests that hepatic drug metabolizing enzymes are saturated. Saturation of enzymes is characteristic of zero-order kinetics, not first-order kinetics, thus this option is incorrect.
05

Analyzing Option (D)

Option (D) states that drug clearance will increase with an increase in plasma drug concentration. In first-order kinetics, drug clearance remains constant regardless of drug concentration, so this is incorrect.
06

Analyzing Option (E)

Option (E) mentions that the rate of drug elimination is proportional to plasma drug concentration. This is a defining characteristic of first-order elimination, making this option correct.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Drug Half-life
The drug half-life is a key concept in pharmacology. It refers to the time it takes for the concentration of a drug in the plasma to reduce by half. In first-order kinetics, this half-life is constant. This means it does not change regardless of how high or low the drug concentration is in the body.

Some important points to remember about drug half-life in first-order elimination include:
  • The half-life remains the same regardless of the dose, due to the constant proportionate elimination.
  • It is an important concept for determining dosing schedules, ensuring that drug levels remain therapeutic without reaching toxic levels.
Understanding drug half-life can help in predicting how long a drug will stay active within the body, providing essential information for safe and effective dosing.
Plasma Drug Concentration
Plasma drug concentration refers to the amount of the drug present in the plasma at any given time. It is crucial for determining the effectiveness and safety of drug therapy. In first-order kinetics, the rate at which a drug is eliminated from the body's plasma is proportional to its concentration. This means if there is more drug present, more of it will be eliminated per unit of time.

Key points to understand about plasma drug concentration include:
  • The concentration in the blood reflects how much drug is available to reach target tissues.
  • It helps in monitoring therapeutic drug levels to avoid sub-therapeutic or toxic effects.
Monitoring plasma drug concentration is essential in personalized medicine, allowing for adjustments in dosing to meet individual patient needs effectively.
Enzyme Saturation
Enzyme saturation is a concept where the enzymes responsible for metabolizing a drug become saturated with substrate, leading to zero-order kinetics. In zero-order kinetics, drug elimination occurs at a constant rate regardless of the concentration. However, in first-order elimination, enzymes are not saturated, allowing for the proportional relationship between drug concentration and rate of elimination.

For first-order elimination:
  • Enzyme saturation does not occur; enzyme activity is directly proportional to substrate concentration.
  • This results in the rate of drug metabolism increasing with an increase in plasma drug concentration, up to a point.
Understanding enzyme saturation helps distinguish between first-order and zero-order kinetics, which is vital for predicting drug behavior in the body.
Drug Clearance
Drug clearance is a measure of the body's efficiency in eliminating a drug. It is defined as the volume of plasma from which the drug is completely removed per unit time. In first-order kinetics, drug clearance remains constant, irrespective of the plasma drug concentration.

Key features of drug clearance under first-order kinetics include:
  • Clearance provides insight into how effectively a drug can be removed by the liver and kidneys.
  • Consistent clearance rates mean that dosing regimens can be more predictable.
Accurate understanding of drug clearance is essential for effective dosing and to avoid potential drug accumulation, which could lead to toxicity.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

What dose of a drug should be injected intravenously every 8 hours to obtain an average steady-state plasma drug concentration of \(5 \mathrm{mg} / \mathrm{L}\) if the drug's volume of distribution is \(30 \mathrm{~L}\) and its clearance is \(8 \mathrm{~L} / \mathrm{h}\) ? (A) \(40 \mathrm{mg}\) (B) \(80 \mathrm{mg}\) (C) \(160 \mathrm{mg}\) (D) \(320 \mathrm{mg}\) (E) \(400 \mathrm{mg}\)

The volume of distribution of a drug will be greater if the drug (A) is more ionized inside cells than in plasma. (B) is administered very rapidly. (C) is highly ionized in plasma. (D) has poor lipid solubility. (E) has a high molecular weight.

After a person ingests an overdose of an opioid analgesic, the plasma drug concentration is found to be \(32 \mathrm{mg} / \mathrm{L}\). How long will it take to reach a safe plasma concentration of \(2 \mathrm{mg} / \mathrm{L}\) if the drug's half-life is 6 hours? (A) 12 hours (B) 24 hours (C) 48 hours (D) 72 hours (E) 1 week

If food decreases the rate but not the extent of the absorption of a particular drug from the gastrointestinal tract, then taking the drug with food will result in a smaller (A) area under the plasma drug concentration time curve. (B) maximal plasma drug concentration. (C) time at which the maximal plasma drug concentration occurs. (D) fractional bioavailability. (E) total clearance.
See all solutions

Recommended explanations on Biology Textbooks

Communicable Diseases

Read Explanation

Energy Transfers

Read Explanation

Biological Processes

Read Explanation

Responding to Change

Read Explanation

Bioenergetics

Read Explanation

Ecology

Read Explanation
View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.