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Drug excretion 2 Contents '''

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Title: Drug excretion 2 Contents '''


1
Drug excretion 2Contents ...
  • Other routes of excretion
  • Biliary
  • Pulmonary
  • Mammary
  • Salivary

2
Routes of excretion
Major routes of elimination
  • Renal ?
  • Biliary
  • Pulmonary

Significant for other reasons
  • Mammary - Delivery to baby
  • Salivary - Drug monitoring

3
Biliary excretion
Bile formed in large volumes in the liver Most
of the water re-absorbed Concentrated bile
stored in the gall bladder Bile secreted into
the upper small intestine
4
Biliary excretion
  • Similar to kidneys
  • Lipid soluble drugs filter initially, but get
    re-absorbed along with the bulk of the water.
    Not excreted efficiently.
  • Acids and bases have active secretion mechanisms.
  • BUT
  • only works effectively if Mol Wt high enough.
    Limit varies for different species. (gt300-500
    for humans)

5
Biliary excretion
  • Most drugs Mol Wt too low for efficient biliary
    excretion.
  • Conjugation to glucuronide often increases Mol Wt
    sufficiently for biliary excretion.
  • Acetate or glycine generally too small.
  • Bile is significant route of excretion for
  • Glucuronide conjugates (e.g. morphine)
  • Limited number of ionised drugs with very high
  • Mol Wt (e.g. cromoglycate)

6
Entero-hepatic circulation
Free
Conjugates in bile
Liver
Conjugates
Free
Small intestine
Colon
Mainly bacteria in colon that hydrolyse the
conjugates
7
Pulmonary excretion
Excretion via the lungs and breath. Significant
route of excretion for some volatile molecules -
especially anaesthetics.
8
Mammary - (milk)
  • No active secretion, just passive diffusion.
  • Concentration in milk reflects free
    concentration in blood (apart from ion trapping).
  • Milk is slightly acid (pH 7.0) compared to
    blood (pH 7.4).

9
Erythromycin in milk
Blood (pH 7.4) Milk (pH 7.0)
Non-ionised Non-ionised
Ionised Ionised
Lipid
Erythromycin concentrations approx 8 times higher
in milk than blood.
10
Drugs in milk -clinical significance
  • Mainly the effect of the drug on the baby. e.g.
  • Chloramphenicol Possible bone marrow
    suppression.
  • Diazepam Accumulation and sedation.
  • Heroin Prolonged neonatal dependence.
  • Methadone Possible withdrawal syndrome if
    breast feeding stopped suddenly.
  • Propylthiouracil Suppression of thyroid
    function.
  • Tetracycline Permanent staining of infant teeth

11
Saliva
  • Significant because of possible use in drug
    monitoring.
  • Pharmacokinetic experiments often need serial
    blood samples (10 or more). Ethical approval?
    Saliva sampling is non-invasive.
  • Neutral molecules - salivary concentrations do
  • reflect free concentrations in plasma. Has
    been
  • used for antipyrine.
  • Ionised drugs are a problem. Saliva pH is
  • variable - variable degree of ion trapping.

12
Terms with which you should be familiar ...
  • Biliary excretion
  • Pulmonary excretion
  • Mammary excretion
  • Salivary excretion
  • Enterohepatic circulation

13
What you should be able to do
  • Describe how drugs may be added to or removed
    from bile, including the significance of
    molecular weight.
  • Describe the process of enterohepatic
    circulation.
  • Describe the movement of drugs into milk and
    the possible consequences for the baby.
  • Describe the potential for replacing blood
    sampling by saliva sampling.
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