Absorption Flashcards

1
Q

What are the four processes affecting the movement of drugs through the body?

A

Absorption, Distribution, Metabolism, Excretion.

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2
Q

what makes a drug effective, using absorption principal.

A

it must no be inactivated before reaching its first target tissue.

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3
Q

what is bioavailability? What does bioavailability depend on?

A

the fraction of an administered dose of drug that reaches the systemic circulation unchanged. it depends of course on the route it takes in the body.

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4
Q

what is systemic circulation?

A

blood leaving the heart via the aorta to supply all the tissues of the body

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5
Q

What affects the rate of absorption?

A

the duration of dose, intensity of action, and the initial onset.
** also method of injection

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6
Q

There are two routes of administration, Enteral and parenteral. Define them.

A
  1. Enteral- via intestine, used to refer to the oral route of administration.
  2. Parenteral- routes that involve absorption though any other site than the stomach or intestine.
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7
Q

Describe the advantages and disadvantages of Oral administration.

A

A: simple, convenient for self-admin, and is usually safer than injection.
D: Absportion may be erratic, patient compliance problems, possible with unconscious patient, “first-pass” effect, slow

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8
Q

What is the first-pass metabolism?

A

This is when orally are absorbed into the portal vien (PV) and travel first to the liver where metabolism may inactivate a percentage of the drug molecules.

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9
Q

What is unique about drugs that are administered parenterally.

A

Enter the systemic circulation and reach other tissues before undergoing metabolism in the liver.

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10
Q

Describe the advantages and disadvantages of sublingual (under the tongue) administration.

A

its a type of trans-mucosal absorption.
A: relatively simple; no first-pass metabolism.
D: patient must no swallow (cooperate), and significant proportion of dose may be swallows despite efforts not to swallow.

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11
Q

Describe the advantages and disadvantages of subcutaneous injection (SC or SQ) administration.

A

A: suitable for solid pellets, insoluble suspensions, oily vehicles, easier than IV, and absorbs slower than IV, or IM.
D: not for large volumes, pain or necrosis with irritating drugs, absorption can be slow.

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12
Q

Describe the advantages and disadvantages of intramuscular injection (IM).

A

A: suitable for moderate volumes, drugs in aqueous solution will be rapidly absorbed, and those in oily vehicles will be slowly absord. Its safer and esier than IV
D: local pain and swelling possible, absorption slower than IV, avoid during anitcoagulant treatment.

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13
Q

Describe the advantages and disadvantages of intravenous injection (IV).

A

A: emergency use -> rapid onset of activity, large volumes (slowly), and irritating drugs (when diluted)
D: higher risk of adverse effects, often must inject slowly due to cardiac toxicity risk, not for oily or insoluble drugs, and requires more skill to administer.

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14
Q

Describe the advantages and disadvantages of topical administration.

A

(used for eye, ear, skin, mucous membranes)
A: drug delivered to site of need, and can achieve very high concentrations.
D: may be absorbed systemically, and may not remain in place/messy.

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15
Q

Describe the advantages and disadvantages of transdermal administration.

A

A: controlled released prolonged duration of action
D: slow onset of action, excessive absorption may occur if blood flow to skin is excessive.

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16
Q

what is transdermal administration

A

the drug is applied to skin with the intention of having it absorbed into the systemic circulation to produce an effect elsewhere in the body.

17
Q

Name the 5 other routes, that are not that common.

A
intraperitoneal injection (IP)
intradermal injection (ID)
intrathecal (spinal)
intrarectal (sippository)
inhalation.
18
Q

what is drug formulation?

A

Refers to the physical form of a medication as well as its chemical ingredients. Most of the inactive ingredients are present simply to balance pH, to alter flavour, or to produce the desired physical form.

19
Q

What is the difference between non-ionized and ionized molecules?

A

Non-ionized is more lipid soluble, therefore they can diffuse across membranes.
ionized is more water soluble

20
Q

what determines the ionization state of a drug?

A

pKa, 5:20