Drug distribution Flashcards

1
Q

Plasma protein binding

A

Carriers for poorly soluble metabolites

  • drugs drugs bind to these + are transported around circulation
  • reversible binding
  • influence drug pharmacokinetics
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2
Q

How do drugs bind to serum albumin (plasma protein)

A

Thermodynamic motion leads to chance collision

  • Electrostatic binding forces can be overcome by thermal energy
  • 90% drug bound is = 90% of molecule being bounded of the time
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3
Q

Competition for plasma protein binding sites lead to…

A

drug interactions

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4
Q

What drugs can access blood brain barrier

A

Lipophilic/transported drugs can access

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5
Q

Blood brain barrier

A

Effective diffusional barrier

- tight junctions between endothelial cells, pericytes + glial limitans are barriers to drug escape

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6
Q

How can drug enter placenta

A

Drug must pass into maternal blood pool + enter foetal circulation (passive diffusion/active transport)
- risk of teratogenic/embryotoxic effects

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7
Q

Which drugs can/ cannot enter placenta

A

Lipophilic drugs can

Drugs with high plasma protein binding affinity do not

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8
Q

How do drugs enter breastmilk

A

Alveolar apical cells form a tight junction limited lipid barrier between capillaries + alveolar lumen
- diffusion into milk limited by lipophilicity + size

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9
Q

Adipose tissue is a major reservoir for…

A

Lipophilic drugs

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10
Q

Where is adipose tissue

A

Skin (subcutaneous), around intestinal organs (visceral), breasts + bone marrow

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11
Q

What s adipose tissue composed of

A

Adipocytes - cells with large intracellular vacuoles filled with lipids

  • lipid soluble drugs can accumulate in reservoir
  • increase in adipocyte, size in obesity
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12
Q

Which compartments are drugs distributed

A

Extracellular fluid (plasma, interstitial fluid, lymph)
Intracellular fluid (cell contents)
Transcellular fluid (CSF, peritoneal, intraocular, synovial etc.)
Fat
Bound to protein

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13
Q

Volume of distribution

A

Apparent volume of plasma that would accommodate total drug amount at the measured plasma concentration

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14
Q

Calculate Vd

A

total amount of drug/plasma concentration

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15
Q

If Vd is more than 40 litres

A

Indicates some storage of drug in tissue

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16
Q

If Vd is less than 15 litres

A

drug is largely restricted to plasma + interstitial fluid

17
Q

How can critically-ill patients alter distribution parameter

A

Changes in capillary permeability due to inflammation
Decrease in blood pressure and organ perfusion in septic shock
Fluid resuscitation increases Vd

18
Q

How can pre-existing disease alter distribution parameter

A

Hepatic disease causes decrease in serum albumin levels

Renal dysfunction changes fluid volumes

19
Q

How can obesity alter distribution parameter

A

Ideal versus actual body weight

Accumulation of lipophilic drugs and other xenobiotics (e.g. organophosphate poisoning)

20
Q

How can active transport alter distribution parameter

A

Import of drugs across lipid barrier by transporters
Export of drugs from cells by P-glycoproteins
Non-linear relationship between plasma extracellular + intracellular concentrations

21
Q

Distribution of drug after administration is determined by

A

Reversible binding to plasma proteins
Perfusion of tissue by blood
Structure of vascular endothelium
Lipophilicity of drug

22
Q

When choosing antibiotic, must consider…

A

site of infection + drug distribution

23
Q

Aminoglycosides are hydrophilic, can they accumulate in adipose tissue

A

No - danger of toxicity