Pharmacokinetics 5 Flashcards

1
Q

Drug action - targets?

A
  • enzyme
  • receptors
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2
Q

routes of administration examples

A

IV - blood
Oral - gut
IM - Muscle

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3
Q

The drug hits the site of absorption > diffuses through (normally passive) >

A

drug binds to PLASMA PROTEIN

Reversible binding to plasma proteins

Acidic (& neutral) drugs bind to albumin (warfarin)
Basic drugs bind to β-globulins (quinine)

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4
Q

Drug binding with plasma proteins

A

[Free] or [bound] drug is in dynamic equilibrium

High binding to plasma proteins- less available for target action

One drug can displace other drug binding of other drug

(Thermodynamic motion, collision; thermal energy dominate the electrostatic forces)

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5
Q

Distribution of Drugs (influencing factors)

A

Barriers
- cell arrangements
-active transporters
- size and lipid solubility
Blood flow (how well the tissue perfused)
-High: heart, brain, lungs, kidney, glands
-low: skin, muscle
-negligible- bone, teeth, hairs, cartilage

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6
Q

Tissue accumulation (fat depots)

A

Highly lipid soluble drugs accumulate
acute- thiopental
chronic- xenobiotics, benzodiazepines

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7
Q

Blood Brain Barrier (Tight junctions, restricted access to biomolecules)

A

Diffusion only possible for lipid soluble drugs

The integrity compromised during meningitis (allowing access for antibiotics)

Active transport possible (e.g. methylDOPA)

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8
Q

Blood Placental Barrier (Tight junctions, restricted access to biomolecules)

A

Lipid solubility and size of the drug determine the distribution to foetus.

Drug use in pregnancy: Risk adverse/toxic teratogenic effects during pregnancy and neonatal toxicity during labour

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9
Q

Pharmacokinetics- Volume of Distribution

A

A. Drug bound to plasma proteins
B. Fat Deopts
C. Fluid Compartments

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10
Q

40 liters total body fluids
=
components?

A
  • 15 liters Extracellular
  • 3 litres Plasma (fluid)
  • 12 litres Interstitial
    Includes cerebrospinal / matrix
    >90% as a gel
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11
Q

Pharmacokinetics- Volume of Distribution (Vd)

A

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

Vd = total amount of drug (Q) / plasma concentration (Cp)

The total amount of drug (Q) will vary with time due to the elimination

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12
Q

How many litres gets accumulated and restricted?

A

Vd > 40 litres: drug accumulation in tissues

Vd < 10 litres drug restricted to plasma and interstitial fluid (largely)

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13
Q

Pharmacokinetics- Volume of Distribution

A

Drug A
Q (amount of drug)= 200 gms
Plasma concentration, Cp= 10 gms/L (mass/volume)
Volume of distribution = Q/Cp = 200 gms/ 10 gm/L = 20 L
Vol. of distribution (for an average human)= 20 L/60 Kg = 0.33 L/Kg

Drug B
Q (amount of drug)= 200 gms; Plasma concentration, Cp= 1 gm/L

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