Drug Excretion
Drug excretion in Milk.
• Most of the drugs consumed during lactation
are found to be detected in breast milk
• However ,quantitatively insignificant from
mothers point of view but often sufficient
enough to cause harmful effect on suckling
infant, because of inherent toxicity of the
drug.
• The passage of drug to breast milk is by
diffusion
Excretion in milk continued…..
• Drugs which are highly protein bound are less
secreted in milk.
• Milk is slightly Acidic
• Hence basic drugs tend to get concentrated more
in milk than acidic drugs.
• Most drugs are safe, some drugs may suppress
lactation or alter the taste.
• Any drugs to be taken should be done,
immediately after breast feeding or 4 hours
before breast feeding-ensuring that drug gets
cleared.
Drugs contraindicated during
lactation.
• Most of Anti-cancer drugs
• All radio-pharmaceuticals, including radio active
isotopes
• Anti-thyroid drugs including radio active iodine.
• Antimicrobial drugs like
1. Tetracyclines –bone and teeth malformations.
2. Chloramphenicol-grey baby syndrome.
3. Sulfonamides-kernicterus.
4. Quinolones- joint and cartilage damage.
5. INH- Hepatotoxicity.
Drugs contraindicated during lactation
• Hormones
1. Glucocorticoids –supression of body growth
and HPA axis.
2. Contraceptives –supress lactation.
• CNS depressants/sedative hypnotics-induces
sedation, impaired intellectual development,
delayed milestones
• Opoids analgesic –respiratory depression
• Lithium-cardiac arrythmia and supression of
thyroid function.
• Anthracene purgatives-induce abdomonal
cramps
• Anti psychotic
Drugs contraindicated during lactation
• Ephedrine and theophylline - CNS stimulants,
makes child irritable.
• Aspirin – causes Reye s syndrome.
• Among antimicrobials ,penicillin and
cephalosporins are virtually harmless thogh
safe produce abdominal distension and
diarrhoea.
• Bromocriptine and other ergot alkaloids used
deliberately to supress lactation.
Drugs excretion through body
integuments like skin ,hair ,nails.
• Some drugs may get deposited in body
integuments.
• When superficial layers are insensibly lost
,which result in drug excretion.
• Presence of drugs in the above is of
importance in arsenic or mercury poisoning
• Quantitatively insignificant but has medico
legal siginificance.
Pharmacokinetic convention/measures
/parameters.
1. Bioavaliability
2. Volume of distribution
3. Half-life
4. Clearance rate
Half life
• Is defined as the time required for 50% decline
in either concentration or effect of drug.
• Depending upon the ccriteria considered
there are 4 types
1. Plasma half life
2. Biological/elimination
3. Pharmacological
4. physical
1. Plasma half life
• Time required for 50% reduction in plasma
concentration of the drug
• Once peak concentration is achieved, there is
progressive decrease in plasma concentration
of drug
• This is due to drug distribution and disposal
• Plasma concentration decrese in two distinct
phase
• Initial phase of rapid decline-due to
distribution
• Subsequent phase of steady decline –disposal.

Drug Excretion

  • 1.
  • 2.
    Drug excretion inMilk. • Most of the drugs consumed during lactation are found to be detected in breast milk • However ,quantitatively insignificant from mothers point of view but often sufficient enough to cause harmful effect on suckling infant, because of inherent toxicity of the drug. • The passage of drug to breast milk is by diffusion
  • 3.
    Excretion in milkcontinued….. • Drugs which are highly protein bound are less secreted in milk. • Milk is slightly Acidic • Hence basic drugs tend to get concentrated more in milk than acidic drugs. • Most drugs are safe, some drugs may suppress lactation or alter the taste. • Any drugs to be taken should be done, immediately after breast feeding or 4 hours before breast feeding-ensuring that drug gets cleared.
  • 4.
    Drugs contraindicated during lactation. •Most of Anti-cancer drugs • All radio-pharmaceuticals, including radio active isotopes • Anti-thyroid drugs including radio active iodine. • Antimicrobial drugs like 1. Tetracyclines –bone and teeth malformations. 2. Chloramphenicol-grey baby syndrome. 3. Sulfonamides-kernicterus. 4. Quinolones- joint and cartilage damage. 5. INH- Hepatotoxicity.
  • 5.
    Drugs contraindicated duringlactation • Hormones 1. Glucocorticoids –supression of body growth and HPA axis. 2. Contraceptives –supress lactation. • CNS depressants/sedative hypnotics-induces sedation, impaired intellectual development, delayed milestones • Opoids analgesic –respiratory depression • Lithium-cardiac arrythmia and supression of thyroid function. • Anthracene purgatives-induce abdomonal cramps • Anti psychotic
  • 6.
    Drugs contraindicated duringlactation • Ephedrine and theophylline - CNS stimulants, makes child irritable. • Aspirin – causes Reye s syndrome. • Among antimicrobials ,penicillin and cephalosporins are virtually harmless thogh safe produce abdominal distension and diarrhoea. • Bromocriptine and other ergot alkaloids used deliberately to supress lactation.
  • 7.
    Drugs excretion throughbody integuments like skin ,hair ,nails. • Some drugs may get deposited in body integuments. • When superficial layers are insensibly lost ,which result in drug excretion. • Presence of drugs in the above is of importance in arsenic or mercury poisoning • Quantitatively insignificant but has medico legal siginificance.
  • 8.
    Pharmacokinetic convention/measures /parameters. 1. Bioavaliability 2.Volume of distribution 3. Half-life 4. Clearance rate
  • 9.
    Half life • Isdefined as the time required for 50% decline in either concentration or effect of drug. • Depending upon the ccriteria considered there are 4 types 1. Plasma half life 2. Biological/elimination 3. Pharmacological 4. physical
  • 10.
    1. Plasma halflife • Time required for 50% reduction in plasma concentration of the drug • Once peak concentration is achieved, there is progressive decrease in plasma concentration of drug • This is due to drug distribution and disposal • Plasma concentration decrese in two distinct phase • Initial phase of rapid decline-due to distribution • Subsequent phase of steady decline –disposal.