Drug Absorption Elimination

Drug absorption and elimination are pharmacokinetic processes that determine how a medicine enters the body, reaches target tissues, and is removed, shaping its onset, intensity, and duration of action. Absorption transfers drug molecules from the administration site into systemic circulation, while elimination reduces drug concentration through metabolism, primarily in the liver, and excretion, often through the kidneys. Factors such as route of administration, gastrointestinal conditions, blood flow, enzyme activity, and renal function can alter these processes. Understanding them helps clinicians select doses, predict drug interactions, interpret concentration–time profiles, and maintain effective, safe therapy.

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JoVE Core - Pharmacokinetics and Pharmacodynamics

Factors Influencing Drug Absorption: Presystemic Elimination

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2024

The pharmacokinetic journey of oral drugs begins with a crucial first pass through the hepatic portal system, called the first-pass effect. This first pass significantly impacts bioavailability — the proportion of a drug that enters systemic circulation and is available for therapeutic action. The primary route sees the drug absorbed by intestinal membranes and then shunted to the liver via the hepatic portal vein. Here, pre-systemic elimination occurs as drugs face metabolism or biliary...

Drug Absorption: Factors Affecting GI Absorption

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2023

The process of oral drug absorption can be influenced by several factors. Weakly acidic drugs tend to be absorbed more readily from the stomach due to their nonionized state. However, absorption may be less efficient in the upper intestine, where drugs are often ionized. Interestingly, despite the stomach's apparent advantage for drug absorption, its mucous layer can hinder diffusion. Its surface area is also smaller than the intestine's, which can further slow down the absorption rate. In...

Kinetics of Drug Elimination

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2023

Eliminating drugs from the body is a vital process that occurs through excretion or metabolism. Understanding the kinetics of drug elimination is crucial for drug development, dosage determination, and optimizing patient outcomes. Drug clearance depends on the rate of drug elimination and its plasma concentration. Another important parameter is the half-life of a drug, which is the time required for its concentration to decrease by half. In most cases, drug clearance follows first-order...

Drug Elimination: Overview

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2025

Drug elimination involves many complex processes and does not necessarily differentiate between distribution and elimination. It is divided into two primary components: excretion and biotransformation. Excretion refers to removing a drug from the body, either in its unchanged form or as its metabolites. Nonvolatile and polar drugs are primarily excreted through the kidneys, with other pathways including bile, sweat, saliva, and milk. Volatile drugs such as anesthetic gases are excreted via the...

Drug Elimination: Non-Renal Routes

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2023

The liver plays a pivotal role in eliminating drugs and their metabolites, primarily through a process known as biliary excretion. This process involves the hepatocytes, the primary cells in the liver that generate bile. A range of transporters actively expels polar drugs or hydrophilic drug metabolites into the bile, which transports the drugs and metabolites into the small intestine. From here, they are eventually expelled from the body through feces. In some instances, the original drug or a...

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