How Medications Get Absorbed By Your Body

00:04:19
https://www.youtube.com/watch?v=mH81Q9Dtodc

الملخص

TLDRThe video details the process of medication absorption, which is crucial for understanding how drugs enter the bloodstream after administration. It explains different routes of administration including oral, intravenous, intramuscular, and subcutaneous, emphasizing the role of the liver in the first-pass effect that can reduce drug bioavailability. The segment also discusses various drug formulations and their impact on absorption rates, pointing out that factors such as dissolution speed, surface area of absorption, blood flow conditions, lipid solubility, and pH differences significantly influence how effectively a drug is absorbed into the body.

الوجبات الجاهزة

  • 💊 Medication absorption is key for drug effectiveness.
  • 📍 Oral drugs dissolve in the stomach or small intestine.
  • 🏥 IV drugs enter directly into the bloodstream.
  • ⚖️ First-pass effect can reduce bioavailability.
  • 🧬 Drug formulations impact absorption rates.
  • 🔄 Factors like surface area and blood flow affect absorption.
  • 🌡️ High lipid solubility aids in easier absorption.
  • 🥼 pH differences influence drug ionization and absorption.

الجدول الزمني

  • 00:00:00 - 00:04:19

    Medication absorption refers to how a drug moves from its administration site into the bloodstream. Oral drugs dissolve in the stomach or pass to the small intestine, the main absorption site, where they enter the portal venous system to the liver for the first pass effect. This can inactivate part of the drug before it reaches general circulation. Unlike oral drugs, intravenous (IV) drugs enter the bloodstream directly, bypassing the GI tract, while intramuscular and subcutaneous injections also avoid GI absorption. Bioavailability is the degree a drug is absorbed into the bloodstream, with oral drugs typically having less than 100% bioavailability due to the liver's first pass effect, while IV drugs have 100%. Different drug formulations affect absorption rates, with factors like dissolution rate, surface area, blood flow, lipid solubility, and pH differences influencing the absorption process. Faster dissolving drugs are absorbed quicker, and the greater surface area of the small intestine enhances absorption compared to the stomach.

الخريطة الذهنية

فيديو أسئلة وأجوبة

  • What is medication absorption?

    Medication absorption is the movement of a drug from its site of administration into the bloodstream.

  • How are oral drugs absorbed?

    Oral drugs dissolve in the stomach or small intestine and pass through cell membranes into the bloodstream.

  • What is the first-pass effect?

    The first-pass effect is when the liver metabolizes part of the drug before it reaches general circulation.

  • What does bioavailability mean?

    Bioavailability is the net amount of a drug that is actually absorbed into the bloodstream.

  • How does intravenous drug administration differ from oral?

    Intravenous drugs enter directly into the bloodstream, bypassing gastrointestinal absorption.

  • What factors affect drug absorption?

    Factors include rate of dissolution, surface area, blood flow, lipid solubility, and pH partitioning.

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الترجمات
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التمرير التلقائي:
  • 00:00:00
    medication absorption is the movement of
  • 00:00:03
    a drug from its side of administration
  • 00:00:05
    into the blood
  • 00:00:06
    oral drugs enter the stomach where they
  • 00:00:09
    either dissolve
  • 00:00:11
    and pass through the cell membranes of
  • 00:00:14
    epithelial cells lining the stomach
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    or travel undissolved through the
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    stomach to the small intestine which is
  • 00:00:23
    the most common side of absorption
  • 00:00:26
    here drugs dissolve
  • 00:00:28
    and pass through the intestinal wall
  • 00:00:32
    oral drugs then travel through the
  • 00:00:34
    portal venous system to the liver where
  • 00:00:37
    they undergo the first pass effect
  • 00:00:40
    during this process the liver
  • 00:00:42
    metabolizes some of the drug either
  • 00:00:45
    inactivating it
  • 00:00:49
    or excreting it into bile for
  • 00:00:51
    elimination from the body
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    the remaining amount of active drug
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    leaves the liver and reaches General
  • 00:01:00
    circulation and Target organs
  • 00:01:04
    if a drug is administered via
  • 00:01:06
    intravenous injection it passes directly
  • 00:01:10
    into the bloodstream thus bypassing
  • 00:01:13
    absorption in the GI tract
  • 00:01:16
    if administered through intramuscular or
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    subcutaneous injection the drug enters
  • 00:01:23
    either muscle or subcutaneous tissue
  • 00:01:26
    where it passes through gaps between
  • 00:01:28
    cells into capillary walls and then into
  • 00:01:32
    General circulation or Target organs
  • 00:01:35
    also bypassing absorption in the GI
  • 00:01:38
    tract
  • 00:01:42
    bioavailability is the net amount of a
  • 00:01:46
    dose of a drug that is actually absorbed
  • 00:01:48
    into the bloodstream
  • 00:01:51
    the bioavailability of oral drugs is
  • 00:01:55
    less than 100 percent because of the
  • 00:01:57
    first pass effect of the liver
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    in contrast the bioavailability of IV
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    drugs is 100 percent because they are
  • 00:02:08
    not exposed to the first pass effect of
  • 00:02:11
    the liver
  • 00:02:13
    different drug formulations alter
  • 00:02:16
    bioavailability because they are not
  • 00:02:19
    absorbed at the same rate or to the same
  • 00:02:22
    extent
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    for example tablets dissolve at varying
  • 00:02:26
    rates
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    in terracotted drugs dissolve in the
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    small intestine not the stomach because
  • 00:02:34
    gastric emptying time differs between
  • 00:02:37
    individuals absorption times also vary
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    sustain release formulas contain tiny
  • 00:02:44
    spheres that dissolve at different rates
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    resulting in a steady drug release
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    throughout the day but also resulting in
  • 00:02:53
    variable absorption
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    some factors affecting drug absorption
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    are the rate of dissolution drugs that
  • 00:03:04
    dissolve faster are absorbed faster
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    surface area since the lining of the
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    small intestine has more surface area
  • 00:03:14
    than the lining of the stomach most
  • 00:03:17
    drugs are absorbed faster in the small
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    intestine
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    blood flow the greater the concentration
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    gradient between the drug-filled stomach
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    and the rapidly flowing drug-free blood
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    the faster the absorption
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    lipid solubility highly lipid soluble
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    drugs pass through the phospholipids in
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    the cell membrane more easily than drugs
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    of low lipid solubility
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    and pH partitioning absorption is faster
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    when the difference between the pH at
  • 00:03:54
    the site of administration and the pH of
  • 00:03:57
    the plasma attracts more drug molecules
  • 00:04:00
    to ionize in the plasma
الوسوم
  • medication
  • absorption
  • bioavailability
  • first-pass effect
  • drug administration
  • oral drugs
  • IV drugs
  • drug formulation
  • pharmacokinetics
  • dissolution