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Related Concept Videos

Methods for Studying Drug Absorption: In situ01:09

Methods for Studying Drug Absorption: In situ

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In situ experiments, such as the Doluisio method and Single-Pass Perfusion technique, provide critical insights into drug uptake by simulating in vivo conditions for drug absorption.
The Doluisio method involves perfusing a prepared segment of a rat's small intestine with a solution of radiolabeled drug and a non-absorbable marker. This helps to differentiate between absorbed and non-absorbed drug concentrations. The intestinal segment is connected at both ends using tubing and syringes,...
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Drug Absorption: Factors Affecting GI Absorption01:19

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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.
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Methods for Studying Drug Absorption: In vitro01:16

Methods for Studying Drug Absorption: In vitro

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In vitro experiments are crucial for understanding the transport and absorption of drugs through biological materials. These studies employ varied methods such as the diffusion cell method, the everted sac technique, and the everted ring technique.
The diffusion cell method uses a two-compartment cell, including a donor compartment with the drug solution, which simulates the environment where the drug is applied, and a receptor compartment with a buffer solution, which simulates the environment...
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Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport01:23

Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport

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Drugs need to permeate cell membranes to reach their target sites after administration. Orally administered drugs must transcend intestinal epithelial membrane barriers to infiltrate the systemic circulation. Drugs with a molecular weight of less than 500 Daltons diffuse through gaps between neighboring cells, called paracellular pathways.
However, most drugs use the transcellular route, traversing directly through the cell membranes via two mechanisms: passive and active transport. Passive...
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Mineral, Vitamin and Water Absorption01:27

Mineral, Vitamin and Water Absorption

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Electrolytes are essential minerals and ions primarily obtained from the diet and absorbed through the gastrointestinal tract. Most electrolytes are absorbed in the small intestine. While the absorption of iron and calcium primarily occurs in the duodenum, calcium is also absorbed in the jejunum and ileum. In these regions, passive diffusion contributes to its absorption alongside active transport mechanisms in the duodenum. These ions can exit the enterocytes through specialized active...
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Drug Absorption: Overview01:17

Drug Absorption: Overview

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The process of drug absorption signifies the transition of a drug from its site of administration into the plasma. This process is influenced by various factors, including the route of administration, the anatomy of the absorption site, the mechanism of absorption, gut motility, and the drug's physicochemical properties.
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Updated: Mar 17, 2026

Author Spotlight: Experiential Tool for Teaching Active Transport Using Ex Vivo Histidine Uptake
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Selenium absorption by canine jejunum.

P G Reasbeck, G O Barbezat, F L Weber

    Digestive Diseases and Sciences
    |May 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    Selenium absorption in dogs varies by compound. D,L-selenomethionine showed the highest jejunal absorption rate, suggesting active transport mechanisms enhance selenium uptake from amino acid-bound forms.

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    Area of Science:

    • Nutritional Science
    • Gastroenterology
    • Trace Element Metabolism

    Background:

    • Selenium deficiency is linked to diseases in animals and potentially humans.
    • Understanding selenium absorption is crucial for human and animal health.
    • Dietary selenium exists in various chemical forms, influencing its bioavailability.

    Purpose of the Study:

    • To compare the in vivo jejunal absorption rates of different selenium compounds in dogs.
    • To investigate the absorption mechanism of selenium from D,L-selenomethionine.
    • To determine if amino acid-bound selenium is absorbed differently than inorganic selenium.

    Main Methods:

    • Triple-lumen perfusion technique in healthy dogs to measure selenium absorption from the jejunum.
    • Administration of trace amounts of D,L-selenomethionine, D,L-selenocystine, and sodium selenite.
    • Intestinal perfusion with L-[75Se]selenomethionine to track absorption and incorporation in anesthetized dogs.

    Main Results:

    • Selenium absorption rates varied significantly: D,L-selenomethionine (1.97±0.04%/cm) > D,L-selenocystine (1.15±0.06%/cm) > sodium selenite (0.51±0.07%/cm).
    • Studies with L-[75Se]selenomethionine showed quantitative correspondence between luminal disappearance and portal venous appearance (74±6%) and tissue incorporation (24±5%).
    • These findings support active transport for amino acid-bound selenium and potentially diffusion for sodium selenite.

    Conclusions:

    • Amino acid-bound selenium compounds (selenomethionine, selenocystine) are absorbed more efficiently from the canine jejunum than sodium selenite.
    • Active transport mechanisms in the gut mucosa likely facilitate the enhanced absorption of amino acid-bound selenium.
    • Sodium selenite absorption may occur via passive diffusion, resulting in a slower uptake rate.