Pharm Flashcards
For better absorption drug should be
NON IONISED
lipid soluble
More surface area
Acidic drug in acidic medium —-
Non ionised——for absorption
For excretion we can make acidic drug in alkali medium —-forced alkalinization —drugs becomed inonized so can’t be absorbed
DRUG USED FOR IT
Acetazolamide(diuretics)(carbonic anhydrase inhibitor)
(NaHco3)
Forced acidification for ALKALI DRUG
Ascorbic acid
Nh4cl
For absorption——non ionised——acid in acid(same)
In case of toxicity —ionised form can’t absorbed to excrete–so acid in base(opposite)
P glycoprotein inhibitors
VACINE Q
Verapamil
Amiodarone
CYCLOSPORINE
ITRACONAZOLE
nifedipine
ERYTHROMYCIN
QUINIdine
Bio equivalent -
Difference in bio availability less than 20 percet
Fomipizole
Antidote for methyl alcohol((-)alcohol dehydrogenase)
Antodote for heparin(acid)
Protamine sulfate(base)
Avoid hemodialysis
AVOID
amphetamine
Verapamil
Op ,opioids
Imipramine
Digoxin,diazepam(strong plasma binding)
Chloroquine
Inactivation of drug by
Opposite (acid with base)
Forced alkalination
Plasma protein bound
Displacement type reaction
Salicylic acid—
Sulphonamide—
SWAT——salicylic acid—-warfarin,tolbutamide
Sulphonamide—bilirubin———inc UCB——kernicterus in new born
Doesn’t cross BBB
Aminogylcoside—- but cross placenta -deafness
Anticholineesterase-neomycin
Anticholinergic-glycopyrolate
Dopamine
Acidic drug——aspirin(heparin-string acid—-so ionized given iv)
Basic drug——morphine
Basic protein—albumin
Acidic protein— alpha 1 acidglycoprotein
Active drug to active matabolite
Diazepam
Spirinolactone
Primidone
Active metabolites
Oxazepam
Canrenone
Phenobarbitone
Activation of inactive drug
Add something at the end
Levodopa———dopaMINE
minoxidil———minixidilSULPHATE
Enalapril————enalaprilat
All ACE- are PRODRUG EXCEPT
Captopril
Lisinopril
Paracetamol —
phase 1(CYP2E1)–+—-
INH , chronic ALCOHOLIC
PHASE2-+-
N ACETYLA CYSTEINE,methionine
Hepatotoxic dose-10-15 gram
Fatal dose-20-25 gran
Microsomal enzyme cyp
2C 9 -P henytoin(warfarin,losartan)
2C 19- PP I ‘s(except omeprazole(inhibits this cyp -so interacts with clopidigrel activatied by it)
(M/C genetic variation in)
2D 6-b eta blocker,Codeine to morphine
2E1-paracEtamol
3A4–most of the drugs
Microsomal enz inducer
GPRS CELL PHONE
GriseofulviN
PhenytoiN
RifampiciN
St johN wart , smokiN
CarbamazepiNE(auto)
PhenobarbitoNE(induction)
Hoffman elimination
Atracurium———->laudanosine(cns stimulant-seizure)
Highest first pass metabolism
Large Vd
—VERAPAMIL and Imipramine
Skin laceration
—-lignocaine
Heart
——propranolol,nitrates(except ISOSORBID MONO NITRATE-least)
Resp
——theophylline ,salbutamol
Renal excretion
Digoxin
Penicillin’’
DiG—-G F
Pen— TS (inhibited by probenecid)
First order- Fraction
0 order ——amount
Zero waat power
WARFARIN
(aspirin)
Alcohol(from beginning itslef zero)
TOLBUTAMIDE
phenytoin
Aspirin replaces warfarin and tolbutamide from protein binding site